OVARIAN CANCER

Disease State

Ovarian cancer is one of the leading causes of cancer death among women, with a lifetime risk of about 1 in 91 for a woman to develop the disease. Due to the high risk of death associated with ovarian cancer, it is essential to understand the disease's distinct biology to inform patient care.1

Patient and Disease Characteristics

Epidemiology

The incidence of ovarian cancer has been gradually declining over the past few decades, likely due, in part, to the increased use of oral contraceptives and the decrease in use of menopausal hormone therapy.1​

Percent of Cases by Stage at Diagnosis2

5-year Relative Survival by Stage at Diagnosis2

Localized
Regional
Distant
Unknown
5-year Relative Survival (all stages)

Although fewer women are being diagnosed with ovarian cancer, many are still diagnosed at later stages, which significantly impacts their chances of long-term survival.2​ Approximately ~45% of ovarian tumors harbor actionable genomic alterations (AGAs).3-5

Pathobiology

Ovarian cancer can develop when genomic aberrations cause uncontrolled cell growth.6

HRR Pathway Deficiency7,8

In many cases of ovarian cancer, genes involved in the homologous recombination repair (HRR) pathway are mutated. BRCA1/2, for example, are tumor suppressor genes, and as such these mutations will drive tumor formation.
Genomic mutations can cause homologous recombination deficiency (HRD)7​

HRD Phenotype

A common underlying issue in ovarian cancer is HRD, a condition where cells lose their ability to repair damaged DNA.6,7

Patient and Disease Characteristics

Patient care in ovarian cancer relies on the understanding that each patient’s disease is unique. Testing for tumor characteristics is important for identifying appropriate patient care strategies.1

Patient Care Plan

Patient history and characteristics1

Genetics
Age
Pregnancy history
Family history
Menstrual history

Stage of disease1​

Early stage
Locally advanced
Metastatic

Ovarian cancer subtypes1

Epithelial ovarian tumors
Ovarian germ cell tumors
Ovarian stromal tumors

Tumor and molecular characteristics1,9-11

Actionable biomarkers

Patient history and characteristics1

Stage of disease1​

Ovarian cancer subtypes1

Tumor and molecular characteristics1,9-11

Genetics
Age
Pregnancy history
Family history
Menstrual history
Early stage
Locally advanced
Metastatic
Epithelial ovarian tumors
Ovarian germ cell tumors
Ovarian stromal tumors
Actionable biomarkers
AGAs=actionable genomic alterations; BRCA1/2=breast cancer gene 1/2; CTC=circulating tumor cells; HRD=homologous recombination deficiency; MMR=mismatch repair; MSI=microsatellite instability; PARP=poly (ADP-ribose) polymerase.

Learn more about select biomarkers in ovarian cancer

References
1. American Cancer Society. Ovarian Cancer. August 25, 2025. Accessed August 25, 2025. https://www.cancer.org/cancer/types/ovarian-cancer/key-statistics.html. 2. National Cancer Institute, Surveillance, Epidemiology, and End Results Program. Cancer Stat Facts: Ovarian Cancer. Accessed August 18, 2025. https://seer.cancer.gov/statfacts/html/ovary.html. 3. Shen C, et al. Oncotarget. 2016;7(44)71686-71695. doi:10.18632/oncotarget.11994. 4. Turashvili G, et al. Arch Pathol Lab Med. Published online September 16, 2025. doi:10.5858/arpa.2025-0157-CP. 5. Rajapaksha W, et al. Front Drug Deliv. 2024;4:1339936. doi:10.3389/fddev.2024.1339936. 6. Romey M, et al. Mod Pathol. 2024;37(4):100445. doi:10.1016/j.modpat.2024.100445. 7. College of American Pathologists. Homologous Recombination Repair Deficiency (HRD): Brief Review of the Clinical Implication and Methodology of Measurement. Accessed August 22, 2025. https://www.cap.org/member-resources/articles/homologous-recombination-repair-deficiency-hrd-brief-review-of-the-clinical-implication-and-methodology-of-measurement. 8. Oubaddou Y, et al. Asian Pac J Cancer Prev. 2023;24(9):3139-3153. doi:10.31557/APJCP.2023.24.9.3139. 9. Budczies J, et al. J Pathol Clin Res. 2022;8(4):371-382. doi:10.1002/cjp2.271. 10. Fan S, et al. Int Immunopharmacol. 2020;89(Pt A):107126. doi:10.1016/j.intimp.2020.107126. 11. Szczerba A, et al. Cancers (Basel). 2022;14(24):6030. doi:10.3390/cancers14246030.
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