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O&G TopicsGynaecological oncology

O&G · Gynaecological oncology

Epithelial ovarian cancer: FIGO 2021 staging, histotypes and the PARP era

Also known as Epithelial ovarian cancer · Ovarian cancer · Tubo-ovarian cancer · High-grade serous ovarian cancer · HGSC · Advanced ovarian cancer

FRANZCOG fellowship foundation on epithelial ovarian cancer: the FIGO staging of ovarian, fallopian tube and peritoneal cancer reproduced from Berek 2021, the type I and type II pathways, germline BRCA testing, primary debulking vs neoadjuvant chemotherapy (EORTC 55971 and CHORUS), PARP-inhibitor maintenance (SOLO-1, SOLO-2, PRIMA, NOVA, PAOLA-1), and survival by stage.

high14 referencesUpdated 27 July 202613 min readSource-verified · Oct 2026

Checked against its sources on 23 Oct 2026

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Target exams

FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • Ovarian cancer symptoms are often insidious: vague abdominal pain or discomfort, menstrual irregularities, dyspepsia and other mild digestive disturbances
  • About two-thirds of epithelial ovarian cancers are Stage III or IV at diagnosis
  • CA125 may help judge response to chemotherapy but does not contribute to staging
  • Test every woman with high-grade nonmucinous invasive ovarian cancer for BRCA1/2 — ~15% are positive and ~40% of them have no family history
  • Do not screen the general population — USPSTF recommends against CA-125 and TVUS screening in average-risk women
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Practise this topic10 MCQs with explanations

Target exams

FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • Ovarian cancer symptoms are often insidious: vague abdominal pain or discomfort, menstrual irregularities, dyspepsia and other mild digestive disturbances
  • About two-thirds of epithelial ovarian cancers are Stage III or IV at diagnosis
  • CA125 may help judge response to chemotherapy but does not contribute to staging
  • Test every woman with high-grade nonmucinous invasive ovarian cancer for BRCA1/2 — ~15% are positive and ~40% of them have no family history
  • Do not screen the general population — USPSTF recommends against CA-125 and TVUS screening in average-risk women
One-line fellowship answer

Epithelial ovarian cancer arises in the ovary, fallopian tube or peritoneum and is staged by the single FIGO system that has covered all three sites since 2014. About two-thirds of cases are Stage III or IV at diagnosis. Standard treatment is surgical staging and cytoreduction with platinum-based chemotherapy (carboplatin AUC 5 to 6 plus paclitaxel 175 mg/m² every 3 weeks for 6 cycles), and PARP-inhibitor maintenance after response, with the greatest benefit in BRCA-mutated disease. All women with high-grade nonmucinous invasive ovarian cancer should be offered germline BRCA1/2 testing; at least 15 percent carry a mutation. In selected Stage IIIC and IV patients, neoadjuvant chemotherapy and interval debulking gave equivalent survival with less morbidity in the EORTC and CHORUS trials.[1]

A 64-year-old presents with three months of bloating, early satiety and a pelvic mass on examination. CA-125 is 480. CT shows omental cake, peritoneal deposits and ascites. This is ovarian cancer until proven otherwise, and the next questions — fit for primary surgery? BRCA mutation? HRD positive? — drive everything that follows. This topic turns a CT scan into a defensible plan.[1][12]

Overview and definition

Epithelial ovarian cancer (EOC) is the malignant surface-epithelial tumour of the ovary, fallopian tube or peritoneum. FIGO unified ovarian, fallopian tube and primary peritoneal cancer into one staging system in 2014; the 2021 update (Berek et al.) carries that staging through. Because as many as 80 percent of tumours previously classified as high-grade serous carcinoma of the ovary or peritoneum may have originated in the fimbrial end of the fallopian tube, the disease is increasingly reframed as tubo-ovarian cancer.[1][9]

About two-thirds of all epithelial ovarian cancers are Stage III or Stage IV at diagnosis. The largest number of patients is in the 60 to 64 years age group, and the lifetime risk of a woman in the USA developing ovarian cancer is approximately 1 in 70.[1]

The numbers that frame the disease

about two-thirdsStage III or IV at diagnosisFIGO 2021 review
at least 15%Germline BRCA1/2 in high-grade nonmucinous canceralmost 40% of them have no family history
about 20%Hereditary factors overallovarian, tubal and peritoneal cancer
about 1 in 70Lifetime risk (USA)general population
[1]
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References14ShowHide
  1. [1]Berek JS, Renz M, Kehoe S, et al. Cancer of the ovary, fallopian tube, and peritoneum: 2021 update. Int J Gynaecol Obstet, 2021.PMID 34669199
  2. [2]Vergote I, Tropé CG, Amant F, et al. Neoadjuvant chemotherapy or primary surgery in stage IIIC or IV ovarian cancer. N Engl J Med, 2010.PMID 20818904
  3. [3]Kehoe S, Hook J, Nankivell M, et al. Primary chemotherapy versus primary surgery for newly diagnosed advanced ovarian cancer (CHORUS): an open-label, randomised, controlled, non-inferiority trial. Lancet, 2015.PMID 26002111
  4. [4]Moore K, Colombo N, Scambia G, et al. Maintenance Olaparib in Patients with Newly Diagnosed Advanced Ovarian Cancer. N Engl J Med, 2018.PMID 30345884
  5. [5]Banerjee S, Moore KN, Colombo N, et al. Maintenance olaparib for patients with newly diagnosed advanced ovarian cancer and a BRCA mutation (SOLO1/GOG 3004): 5-year follow-up of a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Oncol, 2021.PMID 34715071
  6. [6]Pujade-Lauraine E, Ledermann JA, Selle F, et al. Olaparib tablets as maintenance therapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): a double-blind, randomised, placebo-controlled, phase 3 trial. Lancet Oncol, 2017.PMID 28754483
  7. [7]González-Martín A, Pothuri B, Vergote I, et al. Niraparib in Patients with Newly Diagnosed Advanced Ovarian Cancer. N Engl J Med, 2019.PMID 31562799
  8. [8]Mirza MR, Monk BJ, Herrstedt J, et al. Niraparib Maintenance Therapy in Platinum-Sensitive, Recurrent Ovarian Cancer. N Engl J Med, 2016.PMID 27717299
  9. [9]Przybycin CG, Kurman RJ, Ronnett BM, Shih IeM, Vang R Are all pelvic (nonuterine) serous carcinomas of tubal origin? Am J Surg Pathol, 2010.PMID 20861711
  10. [10]van Driel WJ, Koole SN, Sikorska K, et al. Hyperthermic Intraperitoneal Chemotherapy in Ovarian Cancer. N Engl J Med, 2018.PMID 29342393
  11. [11]Grossman DC, Curry SJ, Owens DK, et al. Screening for Ovarian Cancer: US Preventive Services Task Force Recommendation Statement. JAMA, 2018.PMID 29450531
  12. [12]Vaughan S, Coward JI, Bast RC Jr, Berchuck A, Berek JS, Brenton JD Rethinking ovarian cancer: recommendations for improving outcomes. Nat Rev Cancer, 2011.PMID 21941283
  13. [13]Tewari KS, Burger RA, Enserro D, et al. Final Overall Survival of a Randomized Trial of Bevacizumab for Primary Treatment of Ovarian Cancer. J Clin Oncol, 2019.PMID 31216226
  14. [14]Ray-Coquard I, Pautier P, Pignata S, et al. Olaparib plus Bevacizumab as First-Line Maintenance in Ovarian Cancer. N Engl J Med, 2019.PMID 31851799

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