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Ovarian cancer

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Title: Ovarian cancer  
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Ovarian cancer

Ovarian cancer (human)
Micrograph of a mucinous ovarian carcinoma stained by H&E.
Classification and external resources
Specialty Oncology, gynecology
ICD-10 C56
ICD-9-CM 183, 220
ICD-O varied
DiseasesDB 9418
MedlinePlus 000889
eMedicine med/1698
MeSH D010051

Ovarian cancer is a cancer that begins in an ovary.[1] It results in abnormal cells that have the ability to invade or spread to other parts of the body.[2] When this process begins, symptoms may be vague or not apparent, but they become more noticeable as the cancer progresses. These symptoms may include bloating, pelvic pain, and abdominal swelling, among others.[3] Common areas to which the cancer may spread include the lining of the abdomen, lining of the bowel and bladder, lymph nodes, lungs, and liver.[4][5] The risk of ovarian cancer increases in women who have ovulated more over their lifetime. This includes those who have never had children, those who begin ovulation at a younger age or reach menopause at an older age.[6] Other risk factors include hormone therapy after menopause, fertility medication, and obesity.[1][7] Factors that decrease risk include hormonal birth control, tubal ligation, and breast feeding.[7] About 10% of cases are related to inherited genetic risk; women with mutations in the genes BRCA1 or BRCA2 have about a 50% chance of developing the disease. The most common type of ovarian cancer, comprising more than 95% of cases, is ovarian carcinoma. There are five main subtypes of ovarian carcinoma, of which high-grade serous is most common. These tumors are believed to start in the cells covering the ovaries,[6] though some may form at the Fallopian tubes.[8] Less common types of ovarian cancer include germ cell tumors and sex cord stromal tumors.[6] A diagnosis of ovarian cancer is confirmed through a biopsy of tissue, usually removed during surgery.[3] Screening is not recommended in women who are at average risk, as evidence does not support a reduction in death and the high rate of false positive tests may lead to unneeded surgery, which is accompanied by its own risks.[9] Those at very high risk may have their ovaries removed as a preventive measure.[1] If caught and treated in an early stage, ovarian cancer may be curable. Treatment usually includes some combination of surgery, radiation therapy, and chemotherapy.[3] Outcomes depend on the extent of the disease and the subtype of the cancer present.[6] The overall five-year survival rate in the United States is 45%.[10] Outcomes are worse in the developing world.[6] In 2012, ovarian cancer occurred in 239,000 women and resulted in 152,000 deaths worldwide. This makes it, among women, the seventh-most common cancer and the eighth-most common cause of death from cancer. Death from ovarian cancer is more common in North America and Europe than in Africa and Asia.[6]


  • Signs and symptoms 1
  • Risk factors 2
    • Hormones 2.1
    • Genetics 2.2
    • Environmental factors 2.3
    • Other 2.4
    • Protective factors 2.5
  • Pathophysiology 3
  • Diagnosis 4
    • Examination 4.1
      • Risk scoring 4.1.1
    • Pathology 4.2
      • Epithelial carcinoma 4.2.1
        • Serous carcinoma
          • Primary peritoneal carcinoma
        • Clear-cell carcinoma
        • Clear-cell adenocarcinoma
        • Endometrioid
          • Malignant mixed müllerian tumor (carcinosarcoma)
        • Mucinous
          • Adenocarcinoma
          • Pseudomyxoma peritonei
        • Undifferentiated epithelial
        • Transitional cell tumor
          • Malignant Brenner tumor
          • Transitional cell carcinoma
      • Sex cord stromal tumor 4.2.2
        • Granulosa cell tumor
        • Sertoli-Leydig cell tumor
      • Germ cell tumor 4.2.3
        • Dysgerminoma
        • Choriocarcinoma
        • Immature (solid) teratoma
        • Yolk sac tumor/endodermal sinus tumor
      • Squamous cell carcinoma 4.2.4
      • Mixed tumors 4.2.5
      • Secondary ovarian cancer 4.2.6
      • Low malignant potential tumors 4.2.7
    • Staging 4.3
  • Screening 5
  • Prevention 6
  • Management 7
    • Surgery 7.1
    • Chemotherapy 7.2
    • Radiation therapy 7.3
    • Hormonal therapy 7.4
    • Immunotherapy 7.5
    • Follow-up 7.6
    • Palliative care 7.7
  • Prognosis 8
    • Survival rates 8.1
    • Recurrence rates 8.2
  • Epidemiology 9
  • Society and culture 10
  • Other animals 11
  • Research 12
  • References 13
  • Further reading 14
  • External links 15

Signs and symptoms

Signs and symptoms of ovarian cancer are frequently absent in early stages; even when they do exist, they may be subtle. In most cases, symptoms exist for several months before being recognized and diagnosed, or they may initially be misdiagnosed as a condition such as

  • Ovarian Cancer at American Cancer Society
  • GeneReviews/NCBI/NIH/UW entry on BRCA1 and BRCA2 Hereditary Breast/Ovarian Cancer
  • Interactive Health Tutorials Medline Plus: Ovarian cancer Using animated graphics and you can also listen to the tutorial
  • UK statistics for ovarian cancer
  • Patient information about ovarian cancer from Cancer Research UK
  • What is Ovarian Cancer Infographic, information on ovarian cancer - Mount Sinai Hospital, New York

External links

  • Cannistra SA (December 2004). "Cancer of the ovary". N. Engl. J. Med. 351 (24): 2519–29.  

Further reading

  1. ^ a b c "Ovarian Cancer Prevention (PDQ®)". NCI. December 6, 2013. Retrieved 1 July 2014. 
  2. ^ "Defining Cancer". National Cancer Institute. Retrieved 10 June 2014. 
  3. ^ a b c "Ovarian Epithelial Cancer Treatment (PDQ®)". NCI. 2014-05-12. Retrieved 1 July 2014. 
  4. ^ a b "Treating advanced ovarian cancer". Retrieved 2015-05-16. 
  5. ^ Ruddon, Raymond W. (2007). Cancer biology (4th ed.). Oxford: Oxford University Press. p. 223.  
  6. ^ a b c d e f World Cancer Report 2014. World Health Organization. 2014. pp. Chapter 5.12.  
  7. ^ a b "Ovarian Cancer Prevention (PDQ®)". NCI. 2014-06-20. Retrieved 1 July 2014. 
  8. ^ Piek JM, van Diest PJ, Verheijen RH (2008). "Ovarian carcinogenesis: an alternative hypothesis". Adv. Exp. Med. Biol. Advances in Experimental Medicine and Biology 622: 79–87.  
  9. ^ Moyer VA (Dec 18, 2012). "Screening for ovarian cancer: U.S. Preventive Services Task Force reaffirmation recommendation statement.". Annals of internal medicine 157 (12): 900–4.  
  10. ^ "SEER Stat Fact Sheets: Ovary Cancer". NCI. Retrieved 18 June 2014. 
  11. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc Jayson GC, Kohn EC, Kitchener HC, Ledermann JA (October 2014). "Ovarian cancer". Lancet 384 (9951): 1376–88.  
  12. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb Seiden, Michael V. (2012). "Gynecologic Malignancies". In Longo DL, Kasper DL, Jameson JL, Fauci AS, Hauser SL, Loscalzo J.  
  13. ^ a b "Ovarian cancer symptoms". Retrieved 2015-05-16. 
  14. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah "Ovarian cancer". DynaMed. June 18, 2015. 
  15. ^ Goff BA (June 2012). "Ovarian cancer: screening and early detection". Obstetrics and gynecology clinics of North America 39 (2): 183–94.  
  16. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba Hoffman, Barbara L.; Schorge, John O.; Schaffer, Joseph I.; Halvorson, Lisa M.; Bradshaw, Karen D.; Cunningham, F. Gary (2012). "Epithelial Ovarian Cancer". Williams Gynecology (2nd ed.). McGraw Hill Medical. pp. 853–878.  
  17. ^ a b c d e f g DeCherney, Alan; Nathan, Lauren; Goodwin, T. Murphy; Laufer, Neri; Roman, Ashley (2012). "Pediatric and Adolescent Gynecology". Current Diagnosis & Treatment Obstetrics & Gynecology (11th ed.).  
  18. ^ a b c d e f g h i j k l m n o p "Ovarian cancer risks and causes". Cancer Research UK. 15 January 2014. Retrieved 29 January 2015. 
  19. ^ Manson, JoAnn E.; Bassuk, Shari S. (2012). "The Menopause Transition and Postmenopausal Hormone Therapy". In Longo DL, Kasper DL, Jameson JL, Fauci AS, Hauser SL, Loscalzo J.  
  20. ^ "Ovarian Cancer Prevention (PDQ®)".  
  21. ^ Hjartåker A, Meo MS, Weiderpass E (January 2010). "Alcohol and gynecological cancers: an overview". European Journal of Cancer Prevention 19 (1): 1–10.  
  22. ^ Biswas A, Oh PI, Faulkner GE, Bajaj RR, Silver MA, Mitchell MS, Alter DA (2015). "Sedentary Time and Its Association With Risk for Disease Incidence, Mortality, and Hospitalization in Adults: A Systematic Review and Meta-analysis". Annals of Internal Medicine 162 (2): 123–32.  
  23. ^ Margolies, Liz (7 October 2013). "Ovarian Cancer in Transgender Men". National LGBT Cancer Network. Retrieved 5 May 2015. 
  24. ^ a b Odunsi, Kunle; Pejovic, Tanja; Anderson, Matthew L. (2011). Molecular Biology of Gynecologic Cancers. DeVita, Hellman, and Rosenberg's Cancer: Principles and Practice of Oncology (Wolters Kluwer/Lippincott Williams & Wilkins). pp. 1302–1310.  
  25. ^ "Genetics of Breast and Ovarian Cancer (PDQ®)". NCI. 2 October 2014. Retrieved 27 October 2014. 
  26. ^ Rossing MA, Wicklund KG, Cushing-Haugen KL, Weiss NS (2010-01-28). "Predictive Value of Symptoms for Early Detection of Ovarian Cancer". J Natl Cancer Inst. 102 (4): 222–9.  
  27. ^ a b c Miller RW, Ueland FR (March 2012). "Risk of malignancy in sonographically confirmed ovarian tumors.". Clinical obstetrics and gynecology 55 (1): 52–64.  
  28. ^ "Ovarian cancer tests". Retrieved 2015-05-16. 
  29. ^ Dunn, J. D. (Ed.). Associated Title(s): PROTEOMICS – Clinical Applications 11 (15). Online ISSN: 1615-9861. 
  30. ^ "Guideline CG122. Ovarian cancer: The recognition and initial management of ovarian cancer, Appendix D: Risk of malignancy index (RMI I).". NICE clinical guidelines. April 2011. 
  31. ^ Geomini, Peggy; Kruitwagen, Roy; Bremer, Gérard L.; Cnossen, Jeltsje; Mol, Ben W. J. (Feb 2009). "The accuracy of risk scores in predicting ovarian malignancy: a systematic review". Obstetrics and Gynecology 113 (2 Pt 1): 384–394.  
  32. ^ a b Kosary, Carol L. (2007). "Chapter 16: Cancers of the Ovary" (PDF). In Baguio, RNL; Young, JL; Keel, GE; Eisner, MP; Lin, YD; Horner, M-J. SEER Survival Monograph: Cancer Survival Among Adults: US SEER Program, 1988-2001, Patient and Tumor Characteristics. SEER Program. NIH Pub. No. 07-6215. Bethesda, MD: National Cancer Institute. pp. 133–144. 
  33. ^ a b c d e f g h i "Types of ovarian cancer". Retrieved 2015-05-16. 
  34. ^ a b c Levy, Gary; Purcell; Karen (2013). DeCherney, AH; Nathan, L; Laufer, N; et al., eds. Premalignant & Malignant Disorders of the Ovaries & Oviducts. CURRENT Diagnosis & Treatment: Obstetrics & Gynecology, 11e (McGraw-Hill). 
  35. ^ "Primary peritoneal carcinoma". Retrieved 2015-05-16. 
  36. ^ a b "Ovarian Cancer Staging" (PDF). Society for Gynecologic Oncology. 1 January 2014. 
  37. ^ "How is ovarian cancer staged?". Retrieved July 27, 2010. 
  38. ^ "Diagnosis and Staging". Retrieved July 27, 2010. 
  39. ^ "Stages of ovarian cancer". Retrieved 2015-05-16. 
  40. ^ a b c Croswell, Jennifer M.; Brawley, Otis W.; Kramer, Barnett S. (2012). "Prevention and Early Detection of Cancer". In Longo DL, Kasper DL, Jameson JL, Fauci AS, Hauser SL, Loscalzo J.  
  41. ^ a b c d e "Types of treatment for ovarian cancer". Retrieved 2015-05-16. 
  42. ^ "Surgery for ovarian cancer". Retrieved 2015-05-16. 
  43. ^ Lawrie, TA; Medeiros, LR; Rosa, DD; da Rosa, MI; Edelweiss, MI; Stein, AT; Zelmanowicz, A; Ethur, AB; Zanini, RR (28 February 2013). "Laparoscopy versus laparotomy for FIGO stage I ovarian cancer.". The Cochrane database of systematic reviews 2: CD005344.  
  44. ^ a b "Drugs used for ovarian cancer". Retrieved 2015-05-16. 
  45. ^ Yao, Stephanie (19 December 2014). "FDA approves Lynparza to treat advanced ovarian cancer: First LDT companion diagnostic test also approved to identify appropriate patients". U.S. Food and Drug Administration. 
  46. ^ "Ovarian Cancer Treatments Available". Archived from the original on 2010-08-27. Retrieved July 27, 2010. 
  47. ^ a b "Radiotherapy for ovarian cancer". Retrieved 2015-05-16. 
  48. ^ a b c d e f g h i j k l "Ovarian cancer research". Retrieved 2015-05-16. 
  49. ^ "Follow up for ovarian cancer". Cancer Research UK. 
  50. ^ a b Follow-up care from American Cancer Society. Last Medical Review: 03/21/2013. Last Revised: 02/06/2014
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    • Bhosale P, Peungjesada S, Wei W, Levenback CF, Schmeler K, Rohren E, Macapinlac HA, Iyer RB (August 2010). "Clinical Utility of Positron Emission Tomography/Computed Tomography in the Evaluation of Suspected Recurrent Ovarian Cancer in the Setting of Normal CA-125 Levels". International Journal of Gynecological Cancer 20 (6): 936–944.  
  52. ^ "Chemotherapy for ovarian cancer". Retrieved 2015-05-16. 
  53. ^ "ASCO Provisional Clinical Opinion: The Integration of Palliative Care into Standard Oncology Care". ASCO. Retrieved 20 August 2014. 
  54. ^ Radwany SM, von Gruenigen VE (Mar 2012). "Palliative and end-of-life care for patients with ovarian cancer.". Clinical obstetrics and gynecology 55 (1): 173–84.  
  55. ^ "Survival rates for ovarian cancer". American Cancer Society. April 22, 2013. Retrieved 2013-12-30. 
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    • Smith TJ, Temin S, Alesi ER, Abernethy AP, Balboni TA, Basch EM, Ferrell BR, Loscalzo M, Meier DE, Paice JA, Peppercorn JM, Somerfield M, Stovall E, Von Roenn JH (6 February 2012). "American Society of Clinical Oncology Provisional Clinical Opinion: The Integration of Palliative Care Into Standard Oncology Care". Journal of Clinical Oncology 30 (8): 880–887.  
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    • Lewin SN, Buttin BM, Powell MA, Gibb RK, Rader JS, Mutch DG, Herzog TJ (November 2005). "Resource utilization for ovarian cancer patients at the end of life: How much is too much?". Gynecologic Oncology 99 (2): 261–266.  
  57. ^ "Statistics and outlook for ovarian cancer". Retrieved 2015-05-16. 
  58. ^ a b Survival rates based on SEER incidence and NCHS mortality statistics, as cited by the National Cancer Institute in SEER Stat Fact Sheets — Cancer of the Ovary
  59. ^ Gucalp, Rasim; Dutcher, Janice (2012). "Oncologic Emergencies". In Longo DL, Kasper DL, Jameson JL, Fauci AS, Hauser SL, Loscalzo J.  
  60. ^ "Survival rates for ovarian cancer, by stage". American Cancer Society. Retrieved 29 October 2014. 
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  63. ^ a b c Ramirez, Pedro T.; Gershenson, David M. (September 2013). "Ovarian Cancer". The Merck Manual for Health Care Professionals. 
  64. ^ "Ovarian cancer statistics". Cancer Research UK. Retrieved 28 October 2014. 
  65. ^ Hennessy, Bryan T.; Suh, Grace K.; Markman, Maurie (2011). Kantarjian, HM; Wolff, RA; Koller, CA, eds. Ovarian Cancer. The MD Anderson Manual of Medical Oncology (McGraw-Hill). 
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  75. ^ Menon U, Gentry-Maharaj A, Hallett R, Ryan A, Burnell M, Sharma A, Lewis S, Davies S, Philpott S, Lopes A, Godfrey K, Oram D, Herod J, Williamson K, Seif MW, Scott I, Mould T, Woolas R, Murdoch J, Dobbs S, Amso NN, Leeson S, Cruickshank D, McGuire A, Campbell S, Fallowfield L, Singh N, Dawnay A, Skates SJ, Parmar M, Jacobs I (April 2009). "Sensitivity and specificity of multimodal and ultrasound screening for ovarian cancer, and stage distribution of detected cancers: results of the prevalence screen of the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS)". Lancet Oncol. 10 (4): 327–40.  
  76. ^ Leffers N, Daemen T, Helfrich W, Boezen HM, Cohlen BJ, Melief CJ, Nijman HW (Sep 17, 2014). "Antigen-specific active immunotherapy for ovarian cancer". The Cochrane database of systematic reviews 9: CD007287.  


Research into mitigating side effects of ovarian cancer treatment is also ongoing. Radiation fibrosis, the formation of scar tissue in an area treated with radiation, may be relieved with hyperbaric oxygen therapy, but research has not been completed in this area. Treatment of ovarian cancer may also cause people to experience psychiatric difficulties, including depression. Research is ongoing to determine how counseling and psychotherapy can help people who have ovarian cancer during treatment.[48]

Hormone therapies are a topic of current research in ovarian cancer, particularly, the value of certain medications used to treat breast cancer. These include tamoxifen, letrozole, and anastrozole. Preliminary studies have showed a benefit for tamoxifen in a small number of people with advanced ovarian cancer. Letrozole may help to slow or stop growth of estrogen receptor positive ovarian cancer. Anastrozole is being investigated in postmenopausal people with estrogen receptor-positive cancer.[48]

Tyrosine kinase inhibitors are another investigational drug class that may have applications in ovarian cancer. Angiogenesis inhibitors in the receptor tyrosine kinase inhibitor group, including pazopanib, cediranib, and nintedanib, have also been shown to increase progression free survival (PFS), but their benefit for overall survival has not been investigated as of 2015.[11] Preliminary research showed that cediranib combined with platins in recurrent ovarian cancer increased the time to second recurrence by 3–4 months and increased survival by 3 months.[48] MK-1775 is a tyrosine kinase inhibitor that is being used in combination with paclitaxel and carboplatin in platinum-sensitive cancers with p53 mutations. Nintedanib is being researched as a potential therapy in combination with cyclophosphamide for people with recurrences.[48]

mTOR inhibitors were a highly investigated potential treatment in the 2000s and 2010s, but the side effects of these drugs (particularly hyperglycemia and hyperlipidemia) were not well tolerated and the survival benefit not confirmed. PI3 kinase inhibitors have been of interest, but they tend to be highly toxic and cause diarrhea. Another investigated drug is selumetinib, a MAPK inhibitor. It improved survival, but did not correlate with any mutations found in tumors.[11]

PARP inhibitors have also shown promise in early trials, particularly in people with BRCA gene mutations, since the BRCA protein interacts with the PARP pathway. It is also being studied in recurrent ovarian cancer in general, where preliminary studies have shown longer PFS. Specifically, olaparib has shown greater survival compared to doxorubicin, though this treatment is still being investigated. It is not clear yet which biomarkers are predictive of responsiveness to PARP inhibitors.[11] Rucaparib is another PARP inhibitor being researched in BRCA-positive and BRCA-negative recurrent advanced ovarian cancer. Niraparib is a PARP inhibitor being tested in BRCA-positive recurrent ovarian cancer.[48]

Intraperitoneal chemotherapy has also been under investigation during the 2000s and 2010s for its potential to deliver higher doses of cytotoxic agent to tumors. Preliminary trials with cisplatin and paclitaxel have shown it is not well tolerated, but does improve survival, and more tolerable regimens are being researched.[11] Cisplatin and paclitaxel are both being researched as intraperitoneal chemotherapy agents. A specific chemotherapy regimen for rare clear-cell cancers is also under investigation: irinotecan combined with cisplatin.[48]

While an active area of research, no immunotherapy has been shown to be effective as of 2013.[76] However, trials of the antibody and VEGF inhibitor bevacizumab, which can slow the growth of new blood vessels in the cancer, have shown promising results, especially in combination with pazopanib, which also slows the process of blood vessel growth. Bevacizumab has been particularly effective in preliminary studies on stage-III and -IV cancer[11] and has been cited as having at least a 15% response rate.[12] It is being investigated particularly in mucinous ovarian cancers.[48] Bevacizumab can also be combined with platinum chemotherapy, a combination that has had positive preliminary results in PFS, but equivocal results regarding overall survival. One disadvantage to these treatments is the side effect profile, which includes high blood pressure and proteinuria. The drug can also exacerbate bowel disease, leading to fistulae or bowel perforation. Vintafolide, which consists of an antifolate conjugated with vinblastine, is also in clinical trials; it may prove beneficial because folate receptors are overexpressed in many ovarian cancers.[11] Another potential immunotherapy is trastuzumab (Herceptin), which is active against tumors positive for Her2/neu mutations.[12] Other angiogenesis inhibitors are also being investigated as potential ovarian cancer treatments. Combretastatin and pazopanib are being researched in combination for recurrent ovarian cancer. Trebananib and tasquinimod are other angiogenesis inhibitors being investigated. The monoclonal antibody farletuzumab is being researched as an adjuvant to traditional chemotherapy. Another type of immunotherapy involves vaccines, including TroVax.[48]

Research into various prognostic factors for ovarian cancer is also going on. Recent research shows that thrombocytosis predicts lower survival and higher stage cancer.[11] Ongoing research is also investigating the benefits of surgery for recurrent ovarian cancer.[48]

Researchers are assessing different ways to screen for ovarian cancer. Screening tests that could potentially be used alone or in combination for routine screening include the CA-125 marker and transvaginal ultrasound. Doctors can measure the levels of the CA-125 protein in a woman’s blood; high levels could be a sign of ovarian cancer, but this is not always the case, and not all women with ovarian cancer have high CA-125 levels. Transvaginal ultrasound involves using an ultrasound probe to scan the ovaries from inside the vagina, giving a clearer image than scanning the abdomen. The UK Collaborative Trial of Ovarian Cancer Screening is testing a screening technique that combines CA-125 blood tests with transvaginal ultrasound. Several large studies are going on, but none has identified an effective technique.[11][74] In 2009, however, early results from the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS) showed that a technique combining annual CA-125 tests with ultrasound imaging did help to detect the disease at an early stage.[48][75] However, it's not yet clear if this approach could actually help to save lives—the full results of the trial will be published in 2015. One major problem with screening is no clear progression of the disease from stage I (noninvasive) to stage III (invasive) is seen, and it may not be possible to find cancers before they reach stage III. Another problem is that screening methods tend to find too many suspicious lesions, most of which are not cancer, but malignancy can only be assessed with surgery.[11] The ROCA method combined with transvaginal ultrasonography is being researched in high-risk women to determine if it is a viable screening method. It is also being investigated in normal-risk women as it has shown promise in the wider population.[16] Studies are also in progress to determine if screening helps detect cancer earlier in people with BRCA mutations.[48]


Ovarian tumors have been reported in mares. Reported tumor types include teratoma,[66][67] cystadenocarcinoma,[68] and particularly granulosa cell tumor.[69][70][71][72][73]

Other animals

Society and culture

The rate of ovarian cancer between 1993 and 2008 decreased in women of the 40-49 age cohort and in the 50-64 age cohort, possibly due to this group's widespread adoption of oral contraceptives.[11] This decrease made it the ninth-most common cancer in women.[16]

In the US, ovarian cancer affects 1.3-1.4% and is the cause of death of about 1% of women.[16][63] This made it the fifth-leading cause of cancer-related deaths with an estimated 15,000 deaths in 2008.[12][63] Ovarian cancer represents approximately 4% of cancers diagnosed in women.[14] It occurs more commonly in developed countries.[63] Ovarian cancer is the fifth-most common cancer in women in the UK (around 7,100 women were diagnosed with the disease in 2011), and it is the fifth-most common cause of cancer death in women (around 4,300 women died in 2012).[64] It is the most deadly gynecologic cancer.[16] In 2014, the incidence rate for women in developed countries was about 9.4 per 100,000, compared to 5.0 per 100,000 in developing countries.[11] In the US, the incidence rate in women over 50 is approximately 33 per 100,000.[65] In Europe, Lithuania, Latvia, Ireland, Slovakia, and the Czech Republic have the highest incidences of ovarian cancer, whereas Portugal and Cyprus have the lowest incidences.[14]

The overall lifetime risk is around 1.6%[12] (one woman in 48-70).[14] The risk in the UK is similar, at 1.7% (one woman in 60). Ashkenazi Jewish women carry mutated BRCA alleles at a rate five times that of the rest of the population, putting them at higher risk for ovarian cancer.[11]

Globally, as of 2010, about 160,000 people died from ovarian cancer, up from 113,000 in 1990.[62] As of 2014, more than 220,000 diagnoses of epithelial ovarian cancer were made yearly.[11] In 2010, in the United States, an estimated 21,880 new cases were diagnosed and 13,850 women died of ovarian cancer. Around 1800 of the new diagnoses were sex-cord or stromal tumors.[12] In the United Kingdom as of 2014, approximately 7,000-7,100 yearly diagnoses were made and 4,200 deaths occurred.[11][18] It is the 5th most common cancer in UK women. Ovarian cancer is most commonly diagnosed after menopause,[18] between the ages of 60 and 64. 90% of ovarian cancer occurs in women over the age of 45 and 80% in women over 50.[14]

Ovarian cancer cases diagnosed by age group[58]
Age-standardized death from ovarian cancer per 100,000 inhabitants in 2004[61]
  no data
  less than 0.6
  more than 7


Ovarian cancer frequently recurs after treatment. If a recurrence occurs in advanced disease, it typically occurs within 18 months of initial treatment (18 months progression-free survival). Recurrences can be treated, but the disease-free interval tends to shorten and chemoresistance increases with each recurrence.[11] Low malignant potential tumors rarely relapse, even when fertility-sparing surgery is the treatment of choice. 15% of LMP tumors relapse after unilateral surgery in the previously unaffected ovary, and they are typically easily treated with surgery. More advanced tumors may take up to 20 years to relapse, if they relapse at all, and are only treated with surgery unless the tumor has changed its histological characteristics or grown very quickly. In these cases, and when there is significant ascites, chemotherapy may also be used.[16]

Recurrence rates

Low malignant potential tumors[16]
Stage Relative five-year
survival rate
I 99%
II 98%
III 96%
IV 77%
Fallopian tube carcinoma
Stage Relative five-year
survival rate
I 87%
II 86%
III 52%
IV 40%
Germ cell tumors of the ovary
Stage Relative 5-yr
Survival Rate
I 98%
II 94%
III 87%
IV 69%
Ovarian stromal tumors
Stage Relative five-year
survival rate
I 95%
II 78%
III 65%
IV 35%
Invasive epithelial ovarian cancer
Stage Relative five-year
survival rate
I 90%
IA 94%
IB 92%
IC 85%
II 70%
IIA 78%
IIB 73%
III 39%
IIIA 59%
IIIB 52%
IIIC 39%
IV 17%

The survival rates given below are for the different types of ovarian cancer, according to American Cancer Society.[60] They come from the National Cancer Institute, SEER, and are based on patients diagnosed from 2004 to 2010.

Histologic grade Survival
Low grade 88%
Intermediate grade 58%
High grade 27%
Stage Survival
I 90-95%
II 70-80%
III 20-50%
IV 1-5%

Overall five-year survival rates for all types of ovarian cancer are presented below by stage and histologic grade:[12]

Survival rates

Complications of ovarian cancer can include spread of the cancer to other organs, progressive function loss of various organs, ascites, and intestinal obstructions, which can be fatal. Intestinal obstructions in multiple sites are the most common proximate cause of death.[11] Intestinal obstruction in ovarian cancer can either be a true obstruction, where tumor blocks the intestinal lumen, or a pseudo-obstruction, when tumor prevents normal peristalsis.[59] Continuous accumulation of ascites can be treated by placing a drain that can be self-drained.[11]

Ovarian cancer survival varies significantly with subtype. Dysgerminomas have a very favorable prognosis. In early stages, they have a five-year survival rate of 96.9%.[17] Stage-III dysgerminomas have a five-year survival of 61%; when treated with BEP chemotherapy after incomplete surgical removal, dysgerminomas have a 95% two-year survival rate. Sex-cord/stromal malignancies also have a favorable prognosis; because they are slow-growing, even those with metastatic disease can survive a decade or more.[12] Low malignant potential tumors usually only have a bad prognosis when there are invasive tumor implants found in the peritoneal cavity.[16]

The five-year survival rate for all stages of ovarian cancer is 46%; the one-year survival rate is 72% and the ten-year survival rate is 35%.[57] For cases where a diagnosis is made early in the disease, when the cancer is still confined to the primary site, the five-year survival rate is 92.7%.[58] About 70% of women with advanced disease respond to initial treatment, most of whom attain complete remission, but half of these women experience a recurrence 1–4 years after treatment.[12]

Ovarian cancer metastasizes early in its development, often before it has been diagnosed. High-grade tumors metastasize more readily than low-grade tumors. Typically, tumor cells begin to metastasize by growing in the peritoneal cavity.[12] More than 60% of women presenting with ovarian cancer have stage-III or stage-IV cancer, when it has already spread beyond the ovaries. Ovarian cancers shed cells into the naturally occurring fluid within the abdominal cavity. These cells can then implant on other abdominal (peritoneal) structures, included the uterus, urinary bladder, bowel, lining of the bowel wall, and omentum, forming new tumor growths before cancer is even suspected.

Ovarian cancer usually has a relatively poor prognosis. It is disproportionately deadly because it lacks any clear early detection or screening test, meaning most cases are not diagnosed until they have reached advanced stages.[56] However, in some cases, ovarian cancer recurrences are chronically treatable.[11]

Relative five-year survival of invasive epithelial ovarian cancer by stage[55]


Radiation therapy can be used as part of the palliative care of advanced ovarian cancer, since it can help to shrink tumors that are causing symptoms. Palliative radiotherapy typically lasts for only a few treatments, a much shorter course of therapy than non-palliative radiotherapy.[47]

Palliative care can entail treatment of symptoms and complications of the cancer, including pain, nausea, constipation, ascites, bowel obstruction, edema, and mucositis. Especially if the cancer advances and becomes incurable, treatment of symptoms becomes one of the main goals of therapy. Palliative care can also entail helping with decision-making such as if or when hospice care is appropriate, and the preferred place for the patient at end of life care.[54] Bowel obstruction can be treated with palliative surgery. Other treatments of complications can include total parenteral nutrition, a low-residue diet, and adequate pain control.[11] Bowel obstruction can also be treated with octreotide when palliative surgery is not an option. Cancer can also block the ureters, which can be relieved by a nephrostomy or a ureteric stent. Ascites can be relieved by paracentesis or placement of a drain to increase comfort.[4]

Palliative care focuses on relieving symptoms and increasing or maintaining quality of life. It has been recommended as part of the treatment plan for any person with advanced ovarian cancer or patients with significant symptoms.[53]

Palliative care

Women with ovarian cancer should not have routine surveillance imaging to monitor the cancer unless new symptoms appear or tumor markers begin rising.[51] Imaging without these indications is discouraged because it is unlikely to detect a recurrence, improve survival, and because it has its own costs and side effects.[51] However, CT imaging can be used if desired, though this is not common.[11] If a tumor is easily imaged, imaging may be used to monitor the progress of treatment.[52]

For women with germ-cell tumors, follow-up tests generally include alpha-fetoprotein (AFP) and/or human chorionic gonadotropin. For women with stromal cancers, tests for hormones like estrogen, testosterone, and inhibin are sometimes helpful.[50] Inhibin can also be useful for monitoring the progress of sex-cord tumors, along with mullerian inhibiting substance. AFP can also be used to monitor Sertoli-Leydig tumors.[12]

Specific follow-up depends on, for example, the type and stage of ovarian cancer, the treatment, and the presence of any symptoms. Usually, a check-up appointment is made about every 2 to 3 months initially, followed by twice per year for up to 5 years.[49] For epithelial ovarian cancers, the most common test upon follow-up is CA-125 level. However, treatment based only on elevated CA-125 levels and not any symptoms can increase side effects without any prolongation of life, so the implication of the outcome of a CA-125 test should be discussed before taking it.[50] The recommendation as of 2014 is recurrent cancer may be present if the CA-125 level is twice normal.[11]


Immunotherapy is a topic of current research in ovarian cancer. In some cases, the antibody drug bevacizumab, though still a topic of active research, is used to treat advanced cancer along with chemotherapy.[41] It has been approved for this use in the European Union.[48]


Despite the fact that 60% of ovarian tumors have estrogen receptors, ovarian cancer is only rarely responsive to hormonal treatments. Estrogen alone does not have an effect on the cancer, and tamoxifen and letrozole are rarely effective.[11]

Hormonal therapy

In stage 1c and 2 cancers, radiation therapy is used after surgery if there is the possibility of residual disease in the pelvis but the abdomen is cancer-free. Radiotherapy can also be used in palliative care of advanced cancers. A typical course of radiotherapy for ovarian cancer is 5 days a week for 3–4 weeks. Common side effects of radiotherapy include diarrhea, constipation, and frequent urination.[47]

[12] Radiation therapy does not improve survival in people with well-differentiated tumors.[46]

Dysgerminomas are most effectively treated with radiation,[17] though this can cause infertility and is being phased out in favor of chemotherapy.[12]

Radiation therapy

In people with BRCA mutations, platinum chemotherapy is more effective.[11] Olaparib, a PARP inhibitor, was approved by the U.S. Food and Drug Administration for use in BRCA-associated ovarian cancer that had previously been treated with chemotherapy.[45] Germ-cell tumors and malignant sex-cord/stromal tumors are treated with chemotherapy, though dysgerminomas and sex-cord tumors are not typically very responsive.[12][17]

If ovarian cancer recurs, it is considered partially platinum-sensitive or platinum-resistant, based on the time since the last recurrence treated with platins: partially platinum-sensitive cancers recurred 6–12 months after last treatment, and platinum-resistant cancers have an interval of less than 6 months. Second-line chemotherapy should be given only after the cancer becomes symptomatic, because no difference in survival is seen between treating asymptomatic (elevated CA-125) and symptomatic recurrences. For platinum-sensitive tumors, platins are the drugs of choice for second-line chemotherapy, in combination with other cytotoxic agents. Regimens include carboplatin combined with pegylated liposomal doxorubicin, gemcitabine, or paclitaxel. For platinum-resistant tumors, there are no high-efficacy chemotherapy options. Single-drug regimens (doxorubicin or topotecan) do not have high response rates,[11] but topotecan is used in some cases.[12] Topotecan cannot be used in people with an intestinal blockage. Paclitaxel used alone is another possible regimen, or it may be combined with liposomal doxorubicin, gemcitabine, cisplatin, topotecan, etoposide, or cyclophosphamide.[44]

Chemotherapy in ovarian cancer typically consists of platins, a group of platinum-based drugs. Carboplatin is given in combination with either paclitaxel or docetaxel; the typical combination is carboplatin with paclitaxel. Three-drug regimens have not been found to be more effective.[11] Chemotherapy can be given intravenously or in the peritoneal cavity.[12] Typical cycles of treatment involve one treatment every 3 weeks, repeated for 6 weeks or more.[44]

Chemotherapy has been a general standard of care for ovarian cancer for decades, although with highly variable protocols. Chemotherapy is used after surgery to treat any residual disease, if appropriate. In some cases, there may be reason to perform chemotherapy first, followed by surgery. This is called "neoadjuvant chemotherapy", and is common when a tumor cannot be completely removed or optimally debulked via surgery. If a unilateral salpingo-oophorectomy or other surgery is performed, additional chemotherapy, called "adjuvant chemotherapy", can be given.[11] Chemotherapies used in ovarian cancer include paclitaxel, cisplatin, topotecan, and gemcitabine. Germ-cell malignancies are treated differently - a regimen of bleomycin, etoposide, and cisplatin (BEP chemotherapy) is used.[12] Adjuvant chemotherapy is used in stage 1 cancer typically if the tumor is of a high histologic grade (grade 3) or the highest substage (stage 1c).[41]


It is unclear if laparoscopy or laparotomy is better or worse for FIGO stage I ovarian cancer.[43]

The major side effect of an oophorectomy in younger women is early menopause, which can cause osteoporosis. After surgery, hormone replacement therapy can be considered, especially in younger women. This therapy can consist of a combination of estrogen and progesterone, or estrogen alone. Estrogen alone is safe after hysterectomy; when the uterus is still present, unopposed estrogen dramatically raises the risk of endometrial cancer.[11] People having ovarian cancer surgery are typically hospitalized afterwards for 3–4 days and spend around a month recovering at home.[42] Surgery outcomes are best at hospitals that do a large number of ovarian cancer surgeries.[16]

If ovarian cancer recurs, secondary surgery is sometimes a treatment option. This depends on how easily the tumor can be removed, how much fluid has accumulated in the abdomen, and overall health.[11]

To fully stage ovarian cancer, lymphadenectomy should be included in the surgery, but a significant survival benefit to this practice may not happen.[11] This is particularly important in germ cell tumors because they frequently metastasize to nearby lymph nodes.[12]

In advanced cancers, where complete removal is not an option, as much tumor as possible is removed in a procedure called debulking surgery. This surgery is not always successful, and is less likely to be successful in women with extensive metastases in the peritoneum, stage- IV disease, cancer in the transverse fissure of the liver, mesentery, or diaphragm, and large areas of ascites. Debulking surgery is usually only done once.[11] More complete debulking is associated with better outcomes: women with no macroscopic evidence of disease after debulking have a median survival of 39 months, as opposed to 17 months with less complete surgery.[12] Interval debulking surgery is another protocol used, where neoadjuvant chemotherapy is given, debulking surgery is performed, and chemotherapy is finished after debulking.[41]

Surgery is the preferred treatment and is frequently necessary to obtain a tissue specimen for differential diagnosis via its histology. The type of surgery depends upon how widespread the cancer is when diagnosed (the cancer stage), as well as the presumed type and grade of cancer. The surgeon, who is usually a specialized gynecologic oncology surgeon, may remove one (unilateral oophorectomy) or both ovaries (bilateral oophorectomy), the Fallopian tubes (salpingectomy), the uterus (hysterectomy), and the omentum (omentectomy). Typically, all of these are removed. For low-grade, unilateral stage-IA cancers, only the involved ovary (which must be unruptured) and Fallopian tube will be removed. This can be done especially in young people who wish to preserve their fertility. However, a risk of microscopic metastases exists and staging must be completed.[11] If any metastases are found, a second surgery to remove the remaining ovary and uterus is needed.[41] If a tumor in a premenopausal woman is determined to be a low malignant potential tumor during surgery, and it is clearly stage I cancer, only the affected ovary is removed. For postmenopausal women with low malignant potential tumors, hysterectomy with bilateral salpingo-oophorectomy is still the preferred option. During staging, the appendix should be examined or removed. This is particularly important with mucinous tumors.[16] In children or adolescents with ovarian cancer, surgeons typically attempt to preserve one ovary to allow for the completion of puberty, but if the cancer has spread, this is not always possible. Dysgerminomas in particular tend to affect both ovaries: 8-15% of dysgerminomas are present in both ovaries.[17] People with low-grade (well-differentiated) tumors are typically treated only with surgery,[12] which is often curative.[33]


Treatment usually involves chemotherapy and surgery, and sometimes radiotherapy, regardless of the subtype of ovarian cancer.[33] Surgical treatment may be sufficient for well-differentiated malignant tumors and confined to the ovary. Addition of chemotherapy may be required for more aggressive tumors confined to the ovary. For patients with advanced disease, a combination of surgical reduction with a combination chemotherapy regimen is standard. Borderline tumors, even following spread outside of the ovary, are managed well with surgery, and chemotherapy is not seen as useful.[41]


People with a significant family history for ovarian cancer are often referred to a genetic counselor to see if they should be tested for BRCA mutations.[16]

People with strong genetic risk for ovarian cancer may consider the surgical removal of their ovaries as a preventative measure. This is often done after completion of childbearing years. This reduces the chances of developing both breast cancer (by around 50%) and ovarian cancer (by about 96%) in people at high risk. Women with BRCA gene mutations usually also have their Fallopian tubes removed at the same time (salpingo-oophorectomy), since they also have an increased risk of Fallopian tube cancer. However, these statistics may overestimate the risk reduction because of how they have been studied.[12][40]


Ovarian cancer has low prevalence, even in the high-risk group of women from the ages of 50 to 60 (about one in 2000), and screening of women with average risk is more likely to give ambiguous results than detect a problem which requires treatment. Because ambiguous results are more likely than detection of a treatable problem, and because the usual response to ambiguous results is invasive interventions, in women of average risk, the potential harms of having screening without an indication outweigh the potential benefits. The purpose of screening is to diagnose ovarian cancer at an early stage, when it is more likely to be treated successfully.[12][40] Screening with transvaginal ultrasound, pelvic examination, and CA-125 levels can be used instead of prophylactic surgery in women who have BRCA1 or BRCA2 mutations. This strategy has shown some success.[16]

The only screening recommended for all women is an annual pelvic examination. This is not very effective in detecting early ovarian cancer because it is usually only palpable in advanced stages.[16] Ovarian cancer screening is of high clinical interest because the disease is not typically detectable at its early stages, when it is the most curable. Screening is not recommended using CA-125 measurements, HE4 levels, ultrasound, or adnexal palpation in women who are at average risk. Screening for any type of cancer must be accurate and reliable—it needs to accurately detect the disease and it must not give false positive results in people who do not have cancer.[12][40]


In addition to being staged, like all cancers, ovarian cancer is also graded. The histologic grade of a tumor measures how abnormal or malignant its cells look under the microscope. The four grades indicate the likelihood of the cancer to spread and the higher the grade, the more likely for this to occur. Grade 0 is used to describe noninvasive tumors. Grade 0 cancers are also referred to as borderline tumors.[38] Grade 1 tumors have well differentiated cells (look very similar to the normal tissue) and are the ones with the best prognosis. Grade 2 tumors are also called moderately well-differentiated and they are made up of cells that resemble the normal tissue. Grade 3 tumors have the worst prognosis and their cells are abnormal, referred to as poorly differentiated.[39]

  • Stage I: T1+N0+M0
    • IA: T1a+N0+M0
    • IB: T1b+N0+M0
    • IC: T1c+N0+M0
  • Stage II: T2+N0+M0
    • IIa: T2a+N0+M0
    • IIB: T2b+N0+M0
    • IIC: T2c+N0+M0
  • Stage III: T3+ N0+M0
    • IIIA: T3a+ N0+M0
    • IIIB: T3b+ N0+M0
    • IIIC: T3c+ N0+M0 or Any T+N1+M0
  • Stage IV: Any T+ Any N+M1

The ovarian cancer stages are made up by combining the TNM categories in the following manner:

The AJCC/TNM staging system also contains a Tx and a Nx subcategory which indicates the extent of the tumor cannot be described because of insufficient data, respectively the involvement of the lymph nodes cannot be described because of the same reason.

The M categories in the AJCC/TNM staging system provide information on whether the ovarian cancer has metastasized to distant organs such as liver or lungs. M0 indicates the cancer did not spread to distant organs and M1 category is used for cancer that has spread to other organs of the body.

This staging system also uses N categories to describe cancers that have or not spread to nearby lymph nodes. The two N categories are N0, which indicates the cancerous tumors have not affected the lymph nodes, and N1, which indicates the involvement of lymph nodes close to the tumor.

The AJCC/TNM staging system includes three categories for ovarian cancer, T, N, and M. The T category contains three other subcategories, T1, T2, and T3, each of them being classified according to the place where the tumor has developed (in one or both ovaries, inside or outside the ovary). The T1 category of ovarian cancer describes ovarian tumors that are confined to the ovaries, and which may affect one or both of them. The subsubcategory T1a is used to stage cancer found in only one ovary, which has left the capsule intact and which cannot be found in the fluid taken from the pelvis. Cancer that has not affected the capsule is confined to the inside of the ovaries and cannot be found in the fluid taken from the pelvis, but has affected both ovaries, is staged as T1b. T1c category describes a type of tumor that can affect one or both ovaries, and which has grown through the capsule of an ovary or it is present in the fluid taken from the pelvis. T2 is a more advanced stage of cancer. In this case, the tumor has grown in one or both ovaries and is spread to the uterus, Fallopian tubes, or other pelvic tissues. Stage T2a is used to describe a cancerous tumor that has spread to the uterus or the Fallopian tubes (or both) but which is not present in the fluid taken from the pelvis. Stages T2b and T2c indicate cancer that metastasized to other pelvic tissues than the uterus and Fallopian tubes and which cannot be seen in the fluid taken from the pelvis, respectively tumors that spread to any of the pelvic tissues (including uterus and Fallopian tubes), but which can also be found in the fluid taken from the pelvis. T3 is the stage used to describe cancer that has spread to the peritoneum. This stage provides information on the size of the metastatic tumors (tumors that are located in other areas of the body, but are caused by ovarian cancer). These tumors can be very small, visible only under the microscope (T3a), visible but not larger than 2 cm (T3b) and bigger than 2 cm (T3c).

Para-aortic lymph node metastases are considered regional lymph nodes (Stage IIIC). As there is only one para-aortic lymph node intervening before the thoracic duct on the right side of the body, the ovarian cancer can rapidly spread to distant sites such as the lung.

Stage Description
I Cancer is completely limited to the ovary
IA involves one ovary, capsule intact, no tumor on ovarian surface, negative washings
IB involves both ovaries; capsule intact; no tumor on ovarian surface; negative washings
IC tumor involves one or both ovaries
IC1 surgical spill
IC2 capsule has ruptured or tumor on ovarian surface
IC3 positive ascites or washings
II pelvic extension of the tumor (must be confined to the pelvis) or primary peritoneal tumor, involves one or both ovaries
IIA tumor found on uterus or fallopian tubes
IIB tumor elsewhere in the pelvis
III cancer found outside the pelvis or in the retroperitoneal lymph nodes, involves one or both ovaries
IIIA metastasis in retroperitoneal lymph nodes or microscopic extrapelvic metastasis
IIIA1 metastasis in retroperitoneal lymph nodes
IIIA1(i) the metastasis is less than 10 mm in diameter
IIIA1(ii) the metastasis is greater than 10 mm in diameter
IIIA2 microscopic metastasis in the peritoneum, regardless of retroperitoneal lymph node status
IIIB metastasis in the peritoneum less than or equal to 2 cm in diameter, regardless of retroperitoneal lymph node status; or metastasis to liver or spleen capsule
IIIC metastasis in the peritoneum greater than 2 cm in diameter, regardless of retroperitoneal lymph node status; or metastasis to liver or spleen capsule
IV distant metastasis (i.e. outside of the peritoneum)
IVA pleural effusion containing cancer cells
IVB metastasis to distant organs (including the parenchyma of the spleen or liver), or metastasis to the inguinal and extra-abdominal lymph nodes

The FIGO stages are as follows:[11][36]

Ovarian adenocarcinoma deposit in the mesentery of the small bowel

Ovarian cancer is staged using the FIGO staging system and uses information obtained after surgery, which can include a total abdominal hysterectomy, removal of (usually) both ovaries and Fallopian tubes, (usually) the omentum, pelvic (peritoneal) washings, and pelvic biopsies for cytopathology.[11][12][36] Around 30% of ovarian cancers that appear confined to the ovary have metastasized microscopically, which is why even stage-I cancers must be staged completely.[12] The AJCC stage is the same as the FIGO stage. The AJCC staging system describes the extent of the primary tumor (T), the absence or presence of metastasis to nearby lymph nodes (N), and the absence or presence of distant metastasis (M).[37] The most common stage at diagnosis is stage IIIc, with over 70% of diagnoses.[12]


Low malignant potential ovarian tumors, also called borderline tumors, have some benign and some malignant features.[16] LMP tumors make up approximately 10%-15% of all ovarian tumors.[14][33] They develop earlier than epithelial ovarian cancer, around the age of 40-49. They typically do not have extensive invasion; 10% of LMP tumors have areas of stromal microinvasion (<3mm, <5% of tumor). LMP tumors have other abnormal features, including increased mitosis, changes in cell size or nucleus size, abnormal nuclei, cell stratification, and small projections on cells (papillary projections). Serous and/or mucinous characteristics can be seen on histological examination, and serous histology makes up the overwhelming majority of advanced LMP tumors. More than 80% of LMP tumors are Stage I; 15% are stage II and III and less than 5% are stage IV.[16] Implants of LMP tumors are often non-invasive.[33]

Low malignant potential tumors

Ovarian cancer can also be a secondary cancer, the result of metastasis from a primary cancer elsewhere in the body.[12] About 7% of ovarian cancers are due to metastases, while the rest are primary cancers. Common primary cancers are breast cancer, colon cancer, appendiceal cancer, and stomach cancer (primary gastric cancers that metastasize to the ovary are called Krukenberg tumors).[12] Endometrial cancer and lymphomas can also metastasize to the ovary.[34] Surface epithelial-stromal tumor can originate in the peritoneum (the lining of the abdominal cavity), in which case the ovarian cancer is secondary to primary peritoneal cancer, but treatment is basically the same as for primary surface epithelial-stromal tumor involving the peritoneum.

Secondary ovarian cancer

Mixed tumors contain elements of more than one of the above classes of tumor histology. To be classed as a mixed tumor, the minor type must make up more than 10% of the tumor.[14]

Mixed tumors

Primary ovarian squamous cell carcinomas are rare and have a poor prognosis when advanced. More typically, ovarian squamous cell carcinomas are cervical metastases, areas of differentiation in an endometrioid tumor, or derived from a mature teratoma.[16]

Squamous cell carcinoma

Yolk sac tumor/endodermal sinus tumor
Immature (solid) teratoma

Dysgerminoma accounts for 35% of ovarian cancer in young women.[17] These tumors may have mutations in the KIT gene, a mutation known for its role in gastrointestinal stromal tumor. People with an XY karyotype and ovaries (gonadal dysgenesis) who develop a unilateral dysgerminoma are at risk for a gonadoblastoma in the other ovary, and in this case, both ovaries are usually removed when a unilateral dysgerminoma is discovered. However, in general, dysgerminomas are bilateral 10-15% of the time.[12]


Germ-cell tumors are typically discovered when they become large, palpable masses. However, like sex cord tumors, they can cause ovarian torsion or hemorrhage and, in children, isosexual precocious puberty. They frequently metastasize to nearby lymph nodes, especially para-aortic and pelvic lymph nodes.[12]

Germ cell tumors of the ovary develop from the ovarian germ cells.[33] Germ cell tumor accounts for about 30% of ovarian tumors, but only 5% of ovarian cancers, because most germ-cell tumors are teratomas and most teratomas are benign. Malignant teratomas tend to occur in older women, when one of the germ layers in the tumor develops into a squamous cell carcinoma.[12] Germ-cell tumors tend to occur in young women (20s-30s) and girls, making up 70% of the ovarian cancer seen in that age group.[17] Germ-cell tumors can include dysgerminomas, teratomas, yolk sac tumors/endodermal sinus tumors, and choriocarcinomas, when they arise in the ovary. Some germ-cell tumors have an isochromosome 12, where one arm of chromosome 12 is deleted and replaced with a duplicate of the other.[12] While the overall prognosis of germ-cell tumors is favorable, it can vary substantially with specific histology; for instance, the prognosis of the most common germ cell tumor (dysgerminomas) tends to be good, whilst the second-most common (endodermal sinus tumor) tends to have a poor prognosis. Overall, they metastasize more frequently than epithelial ovarian cancers. In addition, the cancer markers used vary with tumor type: choriocarcinomas are monitored with beta-HCG and endodermal sinus tumors with alpha-fetoprotein.[12]

Germ cell tumor

Sertoli-Leydig cell tumor
Granulosa cell tumor

Sex cord-stromal tumor, including estrogen-producing granulosa cell tumor, the benign thecoma, and virilizing Sertoli-Leydig cell tumor or arrhenoblastoma, accounts for 7% of ovarian cancers. They occur most frequently in women between 50 and 69 years of age, but can occur in women of any age, including young girls. They are not typically aggressive and are usually unilateral.[12] Several different cells from the mesenchyme can give rise to sex-cord or stromal tumors. These include fibroblasts and endocrine cells. The symptoms of a sex-cord or stromal ovarian tumor can differ from other types of ovarian cancer. Common signs and symptoms include ovarian torsion, hemorrhage from or rupture of the tumor, an abdominal mass, and hormonal disruption. In children, isosexual precocious pseudopuberty may occur with granulosa cell tumors since they produce estrogen. These tumors cause abnormalities in menstruation (excessive bleeding, infrequent menstruation, or no menstruation) or postmenopausal bleeding. Because these tumors produce estrogen, they can cause or occur at the same time as endometrial cancer or breast cancer. Other sex-cord/stromal tumors present with distinct symptoms. Sertoli-Leydig cell tumors cause virilization and excessive hair growth due to the production of testosterone and androstenedione, which can also cause Cushing's syndrome in rare cases. Also, sex-cord stromal tumors occur that do not cause a hormonal imbalance, including benign fibromas, which cause ascites and hydrothorax.[12]

Sex cord stromal tumor

Transitional cell carcinomas represent less than 5% of ovarian cancers. Histologically, they appear similar to bladder carcinoma. The prognosis is intermediate - better than most epithelial cancers but worse than malignant Brenner tumors.[16]

Transitional cell carcinoma

Malignant Brenner tumors are rare. Histologically, they have dense fibrous stroma with areas of transitional epithelium, and some squamous differentiation. To be classified as a malignant Brenner tumor, it must have Brenner tumor foci and transitional cell carcinoma. The transitional cell carcinoma component is typically poorly differentiated and resembles urinary tract cancer.[16]

Malignant Brenner tumor
Transitional cell tumor

Undifferentiated cancers - those where the cell type cannot be determined - make up about 10% of epithelial ovarian cancers.[33]

Undifferentiated epithelial

Pseudomyxoma peritonei refers to a collection of encapsulated mucous or gelatinous material in the abdominopelvic cavity, which is very rarely caused by a primary mucinous ovarian tumor. More commonly, it is associated with ovarian metastases of intestinal cancer.[16]

Pseudomyxoma peritonei

Mucinous adenocarcinomas make up 5-10% of epithelial ovarian cancers. Histologically, they are similar to intestinal or cervical adenocarcinomas, and are often actually metastases of appendiceal or colon cancers. Advanced mucinous adenocarcinomas have a poor prognosis, generally worse than serous tumors, and are often resistant to platinum chemotherapy, though they are rare.[16]


Mixed müllerian tumors make up less than 1% of ovarian cancer. They have epithelial and mesenchymal cells visible and tend to have a poor prognosis.[16]

Malignant mixed müllerian tumor (carcinosarcoma)

Endometrioid adenocarcinomas make up approximately 15-20% of epithelial ovarian cancers. Because they are typically low-grade, endometrioid adenocarcinomas have a good prognosis. These tumors frequently co-occur with endometriosis or endometrial cancer.[16]


Clear-cell adenocarcinomas are histopathologically similar to other clear cell carcinomas, with clear cells and hobnail cells. They represent approximately 5-10% of epithelial ovarian cancers and are associated with endometriosis in the pelvic cavity. They are typically early-stage and therefore curable by surgery, but advanced clear-cell adenocarcinomas (approximately 20%) have a poor prognosis and are often resistant to platinum chemotherapy.[16]

Hobnail cells seen in a clear cell carcinoma sample
Clear-cell adenocarcinoma

Clear-cell ovarian carcinomas do not typically respond well to chemotherapy and may be related to endometriosis.[11] They represent approximately 5% of all endometrial cancers. Japanese women develop clear-cell ovarian cancer more frequently than other groups of women.[14]

Clear-cell carcinoma

Primary peritoneal carcinomas develop from the peritoneum, a membrane that covers the abdominal cavity that has the same embryonic origin as the ovary. They are often discussed and classified with ovarian cancers when they affect the ovary.[33][35]

Primary peritoneal carcinoma

50% of the time, serous carcinomas are bilateral, and in 85% of cases, they have spread beyond the ovary at the time of diagnosis. Most have a diameter over 15 cm.[34]

Most people with epithelial ovarian carcinoma, about two-thirds, have a serous carcinoma,[11] though this proportion is estimated as high as 80%.[14][34] Low-grade serous carcinoma is less aggressive than high-grade serous carcinomas, though it does not typically respond well to chemotherapy or hormonal treatments.[11] Serous carcinomas are thought to begin in the Fallopian tube.[33] Histologically, serous adenocarcinomas have psammoma bodies. Low-grade serous adenocarcinomas resemble Fallopian tube epithelium, whereas high-grade serous adenocarcinomas show anaplasia and nuclear atypia.[16]

Serous carcinoma

Surface epithelial-stromal tumour, also known as ovarian epithelial carcinoma, is the most common type of ovarian cancer, representing approximately 90% of ovarian cancers. It includes serous tumour, endometrioid tumor, and mucinous cystadenocarcinoma. Less common tumors are malignant Brenner tumor and transitional cell carcinoma of the ovary. Epithelial ovarian cancers develop from the epithelium, a layer of cells that covers the ovary.[33]

A pathological specimen of ovarian carcinoma

Epithelial carcinoma

Ovarian cancers are histologically and genetically divided into type I or type II. Type I cancers are of low histological grade, and include endometrioid, mucinous, and clear-cell carcinomas. Type II cancers are of higher histological grade and include serous carcinoma and carcinosarcoma.[11]

Percent of
ovarian cancers
in women
age 20+
Histology Five-year
89.7 Surface epithelial-stromal tumor (adenocarcinoma) 54.4
 26.4 Papillary serous cystadenocarcinoma 21.0
 15.9 "Borderline" adenocarcinoma
(underestimated - short data collection interval)
 12.6 Adenocarcinoma, not otherwise specified 18.3
 9.8 Endometrioid tumor 70.9
 5.8 Serous cystadenocarcinoma 44.2
 5.5 Papillary 21.0
 4.2 Mucinous cystadenocarcinoma 77.7
 4.0 Clear-cell ovarian tumor 61.5
 3.4 Mucinous adenocarcinoma 49.1
 1.3 Cystadenocarcinoma 50.7
5.5 Carcinoma
 4.1 Carcinoma not otherwise specified 26.8
 1.1 Sex cord-stromal tumour 87.8
 0.3 Other carcinomas, specified 37.3
1.7 Mullerian tumor 29.8
1.5 Germ cell tumor 91.0
 0.8 Teratoma 89.1
 0.5 Dysgerminoma 96.8
 0.3 Other, specified 85.1
0.6 Not otherwise specified 23.0
0.5 Epidermoid (squamous cell carcinoma) 51.3
0.2 Brenner tumor 67.9
0.2 Other, specified 71.7

Ovarian cancers are classified according to the microscopic appearance of their structures (histology or histopathology). Histology dictates many aspects of clinical treatment, management, and prognosis. The gross pathology of ovarian cancers is very similar regardless of histologic type: tumors have solid and cystic masses.[16] According to SEER, the types of ovarian cancers in women age 20 and over are:[32]

Ovarian cancers in women aged 20+, with area representing relative incidence and color representing five-year relative survival rate[32]


Another method for quantifying risk of ovarian cancer is the Risk of Ovarian Cancer Algorithm (ROCA), observes levels over time and determines if they are increasing rapidly enough to warrant transvaginal ultrasound.[16] The Risk of Ovarian Malignancy algorithm uses CA-125 levels and HE4 levels to calculate the risk of ovarian cancer; it may be more effective than RMI. The Assessment of Different Neoplasias in the Adnexa (ADNEX) model can be used to assess risk of malignancy in an adnexal mass, based on its characteristics and risk factors. The QCancer (Ovary) algorithm is used to predict likelihood of ovarian cancer from risk factors.[14]

Feature RMI 1[11] RMI 2[14][31]

Ultrasound abnormalities:

  • multilocular cyst
  • solid areas
  • ascites
  • intra-abdominal metastases
  • 0 = no abnormality
  • 1 = one abnormality
  • 3 = two or more abnormalities
  • 0 = none
  • 1 = one abnormality
  • 4 = two or more abnormalities
Menopausal score
  • 1 = premenopausal
  • 3 = postmenopausal
  • 1 = premenopausal
  • 4 = postmenopausal
CA-125 Quantity in U/ml Quantity in U/ml

Two methods can be used to determine the ultrasound score and menopausal score, with the resultant scores being referred to as RMI 1 and RMI 2, respectively, depending on what method is used.

RMI = ultrasound score x menopausal score x CA-125 level in U/ml.[11]

The RMI is calculated as:

A widely recognized method of estimating the risk of malignant ovarian cancer is the risk of malignancy index (RMI), calculated based on an initial workup.[11][30] An RMI score of over 200 or 250 is generally felt to indicate high risk for ovarian cancer.[11][14]

Risk scoring

To definitively diagnose ovarian cancer, a surgical procedure to inspect the abdomen is required. This can be an open procedure (laparotomy, incision through the abdominal wall) or keyhole surgery (laparoscopy). During this procedure, suspicious tissue is removed and sent for microscopic analysis. Usually, this includes a unilateral salpingo-oophorectomy, removal of a single affected ovary and Fallopian tube. Fluid from the abdominal cavity can also be analyzed for cancerous cells. If cancer is found, this procedure can also be used to determine the extent of its spread (which is a form of tumor staging).[12]

CT scanning is preferred to assess the extent of the tumor in the abdominopelvic cavity, though magnetic resonance imaging can also be used.[11] CT scanning can also be useful for finding omental caking or differentiating fluid from solid tumor in the abdomen, especially in low malignant potential tumors. However, it may not detect smaller tumors. Sometimes, a chest x-ray is used to detect metastases in the chest or pleural effusion. Another test for metastatic disease, though it is infrequently used, is a barium enema, which can show if the rectosigmoid colon is involved in the disease. Positron emission tomography, bone scans, and paracentesis are of limited use; in fact, paracentesis can cause metastases to form at the needle insertion site and may not provide useful results.[16] However, paracentesis can be used in cases where there is no pelvic mass and ascites is still present.[16] A physician suspecting ovarian cancer may also perform mammography or an endometrial biopsy (in the case of abnormal bleeding) to assess the possibility of breast malignancies and endometrial malignancy, respectively. Vaginal ultrasonography is often the first-line imaging study performed when an adnexal mass is found. Several characteristics of an adnexal mass indicate ovarian malignancy; they usually are solid, irregular, multilocular, and/or large; and they typically have papillary features, central vessels, and/or irregular internal septations.[14]

A physical examination, including a pelvic examination, and a pelvic ultrasound (transvaginal or otherwise) are both essential for diagnosis: physical examination may reveal increased abdominal girth and/or ascites (fluid within the abdominal cavity), while pelvic examination may reveal an ovarian or abdominal mass.[11] An adnexal mass is a significant finding that often indicates ovarian cancer, especially if it is fixed, nodular, irregular, solid, and/or bilateral. Ovaries that can be felt are also a sign of ovarian cancer in postmenopausal women. Other parts of a physical examination for suspected ovarian cancer can include a breast examination and a digital rectal exam.[14]

Current research is looking at ways to consider tumor marker proteomics in combination with other indicators of disease (i.e. radiology and/or symptoms) to improve diagnostic accuracy. The challenge in such an approach is that the disparate prevalence of ovarian cancer means that even testing with very high sensitivity and specificity will still lead to a number of false positive results, which in turn may lead to issues such as performing surgical procedures in which cancer is not found intraoperatively.[29] Genomics approaches have not yet been developed for ovarian cancer.[14]

Use of blood test panels may help in diagnosis.[14][27] The OVA1 panel includes CA-125, beta-2 microglobulin, transferrin, apolipoprotein A1, and transthyretin. OVA1 above 5.0 in premenopausal people and 4.4 in postmenopausal people indicates a high risk for cancer.[16]

A blood test for a marker molecule called CA-125 is useful in differential diagnosis and in follow up of the disease, but it by itself has not been shown to be an effective method to screen for early-stage ovarian cancer due to its unacceptable low sensitivity and specificity.[27] CA-125 levels in premenopausal people over 200 U/mL may indicate ovarian cancer, as may any elevation in CA-125 above 35 U/mL in post-menopausal people. CA-125 levels are not accurate in early stage ovarian cancer, as fully half of stage I ovarian cancer patients have a normal CA-125 level.[14][16] CA-125 may also be elevated in benign (non-cancerous) conditions, including endometriosis, pregnancy, uterine fibroids, menstruation, ovarian cysts, Systemic lupus erythematosus, liver disease, inflammatory bowel disease, and pelvic inflammatory disease.[28] HE4 is another candidate for ovarian cancer testing, though it has not been extensively tested. Other tumor markers for ovarian cancer include CA19-9, CA72-4, CA15-3, immunosuppressive acidic protein, haptoglobin-alpha, OVX1, mesothelin, lysophosphatidic acid, osteopontin, and fibroblast growth factor 23.[14]

When an ovarian malignancy is included in a list of diagnostic possibilities, a limited number of laboratory tests are indicated. A complete blood count and serum electrolyte test should be obtained in all patients;[27] when an ovarian cancer is present, these tests often show a high number of platelets (20-25% of people) and low blood sodium levels due to chemical signals secreted by the tumor.[16] A positive test for inhibin A and inhibin B can indicate a granulosa cell tumor.[14]

Ovarian cancer's early stages (I/II) are difficult to diagnose because most symptoms are nonspecific and thus of little use in diagnosis; as a result, it is rarely diagnosed until it spreads and advances to later stages (III/IV).[26] In patients in whom pregnancy is a possibility, BHCG level should be measured during the diagnosis process. Serum alpha-fetoprotein, neuron-specific enolase, and lactate dehydrogenase should be measured in young girls and adolescents with suspected ovarian tumors as younger patients are more likely to have malignant germ cell tumors.[12][14]

Diagnosis of ovarian cancer starts with a physical examination (including a pelvic examination), a blood test (for CA-125 and sometimes other markers), and transvaginal ultrasound.[12] Sometimes a rectovaginal examination is used to help plan a surgery.[16] The diagnosis must be confirmed with surgery to inspect the abdominal cavity, take biopsies (tissue samples for microscopic analysis), and look for cancer cells in the abdominal fluid. This helps to determine if an ovarian mass is benign or malignant.[12]

Micrograph of serous carcinoma, a type of ovarian cancer, diagnosed in peritoneal fluid
A very large ovarian cancer as seen on CT



Serous carcinomas may develop from serous tubal intraepithelial carcinoma, rather than developing spontaneously from ovarian tissue. Other carcinomas develop from cortical inclusion cysts, which are groups of epithelial ovarian cells inside the stroma.[16]

Almost 100% of rare mucinous carcinomas have mutations in KRAS and amplifications of ERBB2 (also known as Her2/neu).[11] Overall, 20% of ovarian cancers have mutations in Her2/neu.[12]

In 50% of high-grade serous cancers, homologous recombination DNA repair is dysfunctional, as are the notch and FOXM1 signaling pathways. They also almost always have p53 mutations. Other than this, mutations in high-grade serous carcinoma are hard to characterize beyond their high degree of genomic instability. BRCA1 and BRCA2 are essential for homologous recombination DNA repair, and germline mutations in these genes are found in about 15% of people with ovarian cancer.[11] The most common mutations in BRCA1 and BRCA2 are the frameshift mutations that originated in a small founding population of Ashkenazi Jews.[16]

Overall, the most common gene mutations in ovarian cancer occur in NF1, BRCA1, BRCA2, and CDK12. Type-I ovarian cancers, which tend to be less aggressive, tend to have microsatellite instability in several genes, including BRAF, KRAS, and PTEN, which are tumor suppressor genes. Type-II cancers, the more aggressive type, have different genes mutated, including p53, BRCA1, and BRCA2.[11] Low-grade cancers tend to have mutations in KRAS, whereas cancers of any grade that develop from low malignant potential tumors tend to have mutations in p53.[16] Type I cancers tend to develop from precursor lesions.[14] Serous cancers that have BRCA mutations also inevitably have p53 mutations, indicating that the removal of both functional genes is important for cancer to develop.[16]

Ovarian cancer forms when errors in normal ovarian cell growth occur. Usually, when cells grow old or get damaged, they die, and new cells take their place. Cancer starts when new cells form unneeded, and old or damaged cells do not die as they should. The buildup of extra cells often forms a mass of tissue called a growth or tumor. These abnormal cancer cells have many genetic abnormalities that cause them to grow excessively.[25] When an ovary releases an egg, the egg follicle bursts open and becomes the corpus luteum. This structure needs to be repaired by dividing cells in the ovary.[18] Continuous ovulation for a long time means more repair of the ovary by dividing cells, which can acquire mutations in each division.[16]

Mutations found in ovarian cancer subtypes[11][14][24]
Gene mutated Mutation type Subtype Prevalence
AKT1 amplification 3%
AKT2 amplification/mutation 6%,[11] 20%[24]
ARID1A point mutation endometrioid and clear cell
BRAF point mutation low-grade serous 0.5%
BRCA1 nonsense mutation high-grade serous 5%
BRCA2 frameshift mutation high-grade serous 3%
CCND1 amplification 4%
CCND2 upregulation 15%
CCNE1 amplification 20%
CDK12 high-grade serous
CDKN2A downregulation (30%) and deletion (2%) 32%
CTNNB1 clear cell
DICER1 missense mutation nonepithelial 29%
DYNLRB1 (km23) mutation 42%
EGFR amplification/overexpression 20%
ERBB2 (Her2/neu) amplification/overexpression mucinous and low-grade serous 30%
FMS coexpression with CSF-1 50%
JAG1 amplification 2%
JAG2 amplification 3%
KRAS amplification mucinous and low-grade serous 11%
MAML1 amplification and point mutation 2%
MAML2 amplification and point mutation 4%
MAML3 amplification 2%
MLH1 1%
NF1 deletion (8%) and point mutation (4%) high-grade serous 12%
NOTCH3 amplification and point mutation 11%
NRAS low-grade serous
PIK3C3 (PI3K3) amplification/mutation 12-20%
PIK3CA amplification endometrioid and clear cell 18%
PPP2R1A endometrioid and clear cell
PTEN deletion endometrioid and clear cell 7%
RB1 deletion (8%) and point mutation (2%) 10%
TGF-β mutation/overexpression 12%
TP53 mutation/overexpression high-grade serous 20-50%
TβRI mutation 33%
TβRII mutation 25%
USP36 overexpression


A diet that includes large amounts of carotene, fiber, and vitamins with low amounts of fat—specifically, a diet with non-starchy vegetables (e.g. broccoli and onions)—may be protective,[16] though research is still ongoing in this area.[18]

Tubal ligation is protective because carcinogens are unable to reach the ovary and fimbriae via the vagina, uterus, and Fallopian tubes.[12] Tubal ligation is also protective in women with the BRCA1 mutation, but not the BRCA2 mutation.[14] Hysterectomy reduces the risk, and removal of both Fallopian tubes and ovaries (bilateral salpingo-oophorectomy) dramatically reduces the risk of not only ovarian cancer, but breast cancer as well.[11] This is still a topic of research, as the link between hysterectomy and lower ovarian cancer risk is controversial. The reasons that hysterectomy may be protective have not been elucidated as of 2015.[18]

Suppression of ovulation, which would otherwise cause damage to the ovarian epithelium and, consequently, inflammation, is generally protective. This effect can be achieved by having children, taking combined oral contraceptives, and breast feeding, all of which are protective factors.[12] A longer period of breastfeeding correlates with a larger decrease in the risk of ovarian cancer.[18] Each birth decreases risk of ovarian cancer more, and this effect is seen with up to five births. Combined oral contraceptives reduce the risk of ovarian cancer by up to 50%, and the protective effect of combined oral contraceptives can last 25–30 years after they are discontinued.[16][18] The protective effect of combined oral contraceptives may be due to progesterone or to the cessation of ovulation.[18] Regular use of aspirin is associated with a lower risk of ovarian cancer; other NSAIDs do not have a similar protective effect.[14]

Protective factors

Higher levels of C-reactive protein are associated with a higher risk of developing ovarian cancer.[14]

Trans men who have ovaries may be at higher risk of ovarian cancer, but the reason for this is unknown. Potential factors include testosterone therapy and lower rates of protective factors.[23]

Smoking tobacco is associated with a higher risk of mucinous ovarian cancer; after smoking cessation, the risk eventually returns to normal. A diet high in animal fats may be associated with ovarian cancer, but the connection is unclear. Diet seems to play a very small role, if any, in ovarian cancer risk.[18]

Increased age (up to the 70s) is a risk factor for epithelial ovarian cancer because more mutations in cells can accumulate and eventually cause cancer. Those over 80 are at slightly lower risk.[16]

Alcohol consumption does not appear to be related to ovarian cancer.[14][21] Other factors that have been investigated, such as talc use on the perineum, smoking, high levels of vitamin D in the blood, presence of inclusion ovarian cysts, and infection with human papilloma virus (the cause of some cases of cervical cancer), have been disproven as risk factors for ovarian cancer.[11][14] However, the carcinogenicity of perineal talc is controversial, because it can act as an irritant if it travels through the reproductive tract to the ovaries.[16][18] Use of talc elsewhere on the body is unrelated to ovarian cancer.[18] Sitting regularly for prolonged periods is associated with higher mortality from epithelial ovarian cancer. The risk is not negated by regular exercise, though it is lowered.[22]


Cohort studies have found a correlation between dairy consumption and ovarian cancer, but case-control studies do not show this correlation. There is mixed evidence regarding the effect of red meat and processed meat in ovarian cancer.[14]

Industrialized nations, with the exception of Japan, have high rates of epithelial ovarian cancer, which may be due to diet in those countries. White people are at a 30-40% higher risk for ovarian cancer when compared to Black and Hispanic people, likely due to socioeconomic factors: White women tend to have fewer children and different rates of gynecologic surgeries that affect risk for ovarian cancer.[16]

Environmental factors

Several rare genetic disorders are associated with specific subtypes of ovarian cancer. Peutz–Jeghers syndrome, a rare genetic disorder, also predisposes people to sex cord tumour with annular tubules.[11][12] Ollier disease and Maffucci syndrome are associated with granulosa cell tumors in children and may also be associated with Sertoli-Leydig tumors. Benign fibromas are associated with nevoid basal cell carcinoma syndrome.[12]

A strong family history of endometrial cancer, colon cancer, or other gastrointestinal cancers may indicate the presence of a syndrome known as hereditary nonpolyposis colorectal cancer (also known as Lynch syndrome), which confers a higher risk for developing a number of cancers, including ovarian cancer. Lynch syndrome is caused by mutations in mismatch repair genes, including MSH2, MLH1, MLH6, PMS1, and PMS2.[12] The risk of ovarian cancer for an individual with Lynch syndrome is between 10 and 12 percent.[12][16] People of Icelandic descent, European Jewish descent/Ashkenazi Jewish descent, and Hungarian descent are at higher risk for epithelial ovarian cancer.[16]

In the United States, five of 100 women with a first-degree relative with ovarian cancer will eventually get ovarian cancer themselves, placing those with affected family members at triple the risk of women with unaffected family members. Seven of 100 women with two or more relatives with ovarian cancer will eventually get ovarian cancer.[16][20] In general, 5-10% of ovarian cancer cases have a genetic cause.[16] BRCA mutations are associated with high-grade serous nonmucinous epithelial ovarian cancer.[14]

The major genetic risk factor for ovarian cancer is a mutation in BRCA1 or BRCA2 DNA mismatch repair genes, which is present in 10% of ovarian cancer cases. Only one allele need be mutated to place a person at high risk, because the risky mutations are autosomal dominant. The gene can be inherited through either the maternal or paternal line, but has variable penetrance.[12][16] Though mutations in these genes are usually associated with increased risk of breast cancer, they also carry a 30-50% lifetime risk of ovarian cancer, a risk that peaks in a person's 40s and 50s.[12] This risk is also cited as 40-60% and 39-46%.[11][16] Mutations in BRCA2 are less risky than those with BRCA1, with a lifetime risk of 20-40%.[12] This risk is also cited as 12-20%. On average, BRCA-associated cancers develop 15 years before their sporadic counterparts, because people who inherit the mutations on one copy of their gene only need one mutation to start the process of carcinogenesis, whereas people with two normal genes would need to acquire two mutations.[16]

Ovarian and breast cancer patients in a pedigree chart of a family


Before menopause, obesity can increase a person's risk of ovarian cancer, but this risk is not present after menopause. This risk is also relevant in those who are both obese and have never used HRT. A similar association with ovarian cancer appears in taller people.[18]

Endometriosis is another risk factor for ovarian cancer,[18] as is pain with menstruation. Endometriosis is associated with clear-cell and endometrioid subtypes, low-grade serous tumors, stage I and II tumors, grade 1 tumors, and lower mortality.[14]

Long periods of continuous ovulation are thought to be the main non-genetic cause of epithelial ovarian cancer. This is because during the cells are constantly stimulated to divide while ovulatory cycles continue. Therefore, people who have not borne children are at twice the risk of ovarian cancer than those who have. A longer period of ovulation caused by early first menstruation or late menopause is also a risk factor.[16][18]

Hormonal conditions such as polycystic ovary syndrome and endometriosis are associated with ovarian cancer, but the link is not completely confirmed.[11] Postmenopausal hormone replacement therapy (HRT) with estrogen likely increases the risk of ovarian cancer. The association has not been confirmed in a large-scale study,[16][19] but notable studies including the Million Women Study have supported this link. Postmenopausal HRT with combined estrogen and progesterone may increase contemporaneous risk if used for over 5 years, but this risk returns to normal after cessation of therapy. Research is divided on the role of intrauterine devices (IUDs) in causing ovarian cancers. Some studies show that short-term use of the IUD can decrease risk of ovarian cancer, but that long-term use of the IUD increases the risk; others show that use of the IUD slightly increases risk when used for any amount of time.[18] Estrogen HRT with or without progestins increases the risk of endometrioid and serous tumors but lowers the risk of mucinous tumors. Higher doses of estrogen increase this risk.[14]

Use of fertility medication may contribute to borderline ovarian tumor formation, but the link between the two is disputed and difficult to study.[11] Fertility drugs may be associated with a higher risk of borderline tumors.[14] Those who have been treated for infertility but remain nulliparous are at higher risk for epithelial ovarian cancer; however, those who are successfully treated for infertility and subsequently give birth are at no higher risk. This may be due to shedding of precancerous cells during pregnancy, but the cause remains unclear.[16] The risk factor may instead be infertility itself, not the treatment.[18]


Things that halt ovulation: breast feeding, oral contraceptive use with estrogen/progesterone combination meds, multiple pregnancies, and pregnancy at an early age, all decrease risk of ovarian cancer. These conditions decrease the overall time during one's lifetime spent ovulating. A positive family history of ovarian cancer is a risk factor for ovarian cancer. People with hereditary nonpolyposis colon cancer (Lynch Syndrome), and persons with BRCA-1 and BRCA-2 genetic abnormalities are at increased risk.

Most of the risk for ovarian cancer is related to the amount of time spent in ovulation. Thus not having children is a risk factor for ovarian cancer, likely because ovulation is not suppressed due to pregnancy. Both obesity and hormone replacement therapy also raise the risk.[12]

Risk factors

Ovarian cancer symptoms can vary based on the subtype.[12] Low malignant potential (LMP) tumors, also known as borderline tumors, do not cause an increase in CA125 levels and are not identifiable with an ultrasound. The typical symptoms of a LMP tumor can include abdominal distension or pelvic pain. Particularly large masses tend to be benign or borderline.[16]

In adolescents or children with ovarian tumors, the presenting symptoms can include severe abdominal pain, irritation of the peritoneum, or bleeding.[17] As the cancer becomes more advanced, it can cause an accumulation of fluid in the abdomen. If the malignancy has not been diagnosed by the time it causes ascites, it is typically diagnosed shortly thereafter.[12] Advanced cancers can also cause abdominal masses, lymph node masses, or pleural effusion.[14]

[14].Sister Mary Joseph nodule Metastases may cause a [16][15][12] If these symptoms start to occur more often or more severely than usual, especially after no significant history of such symptoms, ovarian cancer should be considered.[14][13][12]

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