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Any hereditary breast ovarian cancer syndrome in which the cause of the disease is a mutation in the BRCA2 gene.
Features include: Breast carcinoma and Ovarian neoplasm.
BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC) is characterized by an increased risk for male and female breast cancer, ovarian cancer (including fallopian tube and primary peritoneal cancers), and to a lesser extent other cancers such as prostate, pancreatic, and melanoma, primarily in individuals with a BRCA2 pathogenic variant. Estimates of malignancy risk vary considerably depending on the context in which they were derived. is a summary of the risk for malignancy in an individual with a germline BRCA1 or BRCA2 pathogenic variant.
Table 2.
Risk of Malignancy in Individuals with a Germline BRCA1 or BRCA2 Pathogenic Variant
Cancer Type | General Population Risk | Risk for Malignancy1
| BRCA2
| 12% | 55%-72% by age 70 | 45%-69%
| 2%...
Source: GeneReviews — "BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer"
BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC) should be suspected in individuals with a personal or family history (first-, second-, or third-degree relative in either lineage) of any of the following:
Source: GeneReviews — "BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer"
Syndromic breast cancer. Individuals with the following cancer susceptibility syndromes have an elevated breast cancer risk. In many instances, BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC) can be distinguished from these other disorders based on the constellation of tumors present in the family; however, in some cases, molecular genetic testing may be necessary to differentiate the disorders. Table 3. Genes Associated with Cancer Susceptibility to Consider in the Differential Diagnosis of BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer
Gene(s) | Cancer Susceptibility Syndrome | MOI | Associated Cancers / Distinctive Features |
|---|---|---|---|
High-penetrance (high-risk) genes for breast cancer ATM | ATM c.7271TG | AD | Specific ATM pathogenic variants (e.g., c.7271TG) are assoc w/high-penetrance breast cancer; heterozygosity for most other ATM pathogenic variants is assoc w/moderate-penetrance breast cancer (see below).1 CDH1 |
Hereditary diffuse gastric cancer | AD | Breast cancer (lobular), diffuse gastric cancer. Majority of cancers occur before age 40 yrs. |
Biomarker and diagnostic research for breast-ovarian cancer, familial, susceptibility to, 2 has been reported in the published literature.
No approved treatments are currently available for breast-ovarian cancer, familial, susceptibility to, 2. The disease remains an area of unmet medical need.
Individuals who have a germline pathogenic variant in BRCA1 or BRCA2 are counseled at the time of disclosure of molecular genetic test results about their options for and .
Breast cancer. National Comprehensive Cancer Network (NCCN) guidelines suggest that women with a BRCA1 or BRCA2 pathogenic variant could consider bilateral mastectomy as a primary surgical treatment of breast cancer because of their elevated rate of ipsilateral and contralateral breast cancer (NCCN Guidelines; no-fee registration and login required). PARP inhibitors have emerged as a promising treatment in individuals with BRCA1- and BRCA2-associated breast cancer, given their role in DNA repair. Because BRCA1, BRCA2, and PARP participate in DNA repair, their mutual disruption could lead to "synergistic lethality" of tumor cells. PARP inhibitors were first studied in women with BRCA1- and BRCA2-associated metastatic breast cancer. Significant improvement was seen in in progression-free survival, leading to FDA approval of olaparib for women with locally advanced metastatic breast cancer in 2017 . In a recent randomized, double-blind Phase III trial, olaparib also improved progression-free survival in individuals with early, high-risk, human epidermal growth factor receptor 2-negative BRCA1- and BRCA2-associated breast cancer in the adjuvant setting . Ovarian cancer.
Source: GeneReviews — "BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer"
No data specific to individuals with BRCA1 or BRCA2 pathogenic variants are available.
Source: GeneReviews — "BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer"
Several ongoing studies are investigating novel approaches to the treatment of BRCA1- and BRCA2-associated breast and ovarian cancer. The majority of these studies involve PARP inhibitors. Several prospective and randomized clinical trials are investigating PARP inhibitor treatment of metastatic pancreatic cancer . Studies to identify biomarkers of disease resistance and expected treatment toxicity are also under way . Additional clinical trials are exploring the use of other PARP inhibitors alone or in combination with other systemic treatments. Search ClinicalTrials.gov in the US and EU Clinical Trials Register in Europe for information on clinical studies.
Source: GeneReviews — "BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer"
View trials for breast-ovarian cancer, familial, susceptibility to, 2
Table 4.
Recommended Surveillance for Women with BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer
System/Concern | Evaluation | Frequency
| Breast self-exam | Monthly
Clinical breast exam | Every 6-12 mos beginning at age 25 yrs
Mammogram | Annually beginning at age 30 yrs
Breast MRI | Annually beginning at age 25 yrs or earlier if breast cancer was diagnosed in family member age 30 yrs
| Screening not recommended1 |
| Skin exam w/dermatologist | Individualized based on family history
Pancreatic
cancer | In asymptomatic persons who meet criteria based on mutation status family history, contrast-enhanced MRI/MRCP /or EUS may be considered in a research setting to better delineate the risks benefits of pancreatic cancer screening. |
EUS = endoscopic ultrasound; MRCP = magnetic resonance cholangiopancreatography
1. For women who have not elected to undergo prophylactic bilateral salpingo-oophorectomy: while some clinicians conduct annual transvaginal ultrasound and/or CA-125 concentration, these modalities have not been effective in detecting early-stage ovarian cancer, either in high-risk or in average-risk women.
Table 5.
Recommended Surveillance for Men with BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer
System/Concern | Evaluation | Frequency
| Breast self-exam training | At the time of identification of a BRCA1 or BRCA2 pathogenic variant
Breast self-exam | Monthly beginning at age 35 yrs
Source: GeneReviews — "BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer"
No clinical trials have been registered for breast-ovarian cancer, familial, susceptibility to, 2.
170 publications have been identified in PubMed for breast-ovarian cancer, familial, susceptibility to, 2. Research spans Epidemiology / Natural History (28%), Diagnostic / Biomarker (21%), and Review / Meta-Analysis (21%).
Research Type | Count | % of Total |
|---|---|---|
Disease patterns and progression | 48 | 28% |
Testing and diagnosis research | 36 | 21% |
Research summaries | 36 | 21% |
Laboratory research | 32 | 19% |
Patient case studies | 8 | 5% |
Clinical study results | 7 | 4% |
New treatment approaches | 2 | 1% |
Other research | 1 | 1% |
Wang T (2026). [PMID: 41276771](https://pubmed.ncbi.nlm.nih.gov/41276771/). *Ann Surg Oncol*. [Clinical Trial Publication]
Statman MR (2026). [PMID: 41577648](https://pubmed.ncbi.nlm.nih.gov/41577648/). *Psychooncology*. [Epidemiology / Natural History]
Bonamici L (2026). [PMID: 41488399](https://pubmed.ncbi.nlm.nih.gov/41488399/). *Hum Mutat*. [Diagnostic / Biomarker]
Calzone K (2026). [PMID: 41846226](https://pubmed.ncbi.nlm.nih.gov/41846226/). *Semin Oncol Nurs*. [Review / Meta-Analysis]
Raspin K (2026). [PMID: 41212395](https://pubmed.ncbi.nlm.nih.gov/41212395/). *Patient*. [Review / Meta-Analysis]
Cheng HH (2026). [PMID: 41671423](https://pubmed.ncbi.nlm.nih.gov/41671423/). *J Natl Compr Canc Netw*. [Review / Meta-Analysis]
Perez L (2026). [PMID: 41589845](https://pubmed.ncbi.nlm.nih.gov/41589845/). *Menopause*. [Epidemiology / Natural History]
Edmunds K (2026). [PMID: 41579216](https://pubmed.ncbi.nlm.nih.gov/41579216/). *Fam Cancer*. [Diagnostic / Biomarker]
Baraian CS (2026). [PMID: 41899580](https://pubmed.ncbi.nlm.nih.gov/41899580/). *Cancers (Basel)*. [Review / Meta-Analysis]
Jurgiel WA (2026). [PMID: 41538105](https://pubmed.ncbi.nlm.nih.gov/41538105/). *Discov Oncol*. [Review / Meta-Analysis]
Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 1:46 AM UTC
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Online Mendelian Inheritance in Man
— |
PALB2 | PALB2-related cancer susceptibility (OMIM 620442) | AD | Breast cancer ≤58%,2 ovarian cancer, male breast cancer, pancreatic cancer PTEN |
PTEN hamartoma tumor syndrome | AD | Breast cancer. Other cancers: thyroid, renal cell carcinoma, endometrial, colorectal. Multiple hamartomas, macrocephaly, trichilemmomas, papillomatous papules. Affected persons usually present by late 20s. STK11 | — |
Peutz-Jeghers syndrome | AD | Breast cancer. Other cancers: GI, ovarian (mostly SCTAT), cervical (adenoma malignum), pancreatic, Sertoli cell testicular. GI polyposis, mucocutaneous pigmentation, hyperpigmented macules on fingers. TP53 | — |
Li-Fraumeni syndrome | AD | Breast cancer (often premenopausal). Other cancers: soft tissue sarcoma, osteosarcoma, brain, adrenocortical carcinoma, leukemias. Early-onset multiple primary cancers. Moderate-penetrance (moderate-risk) genes for breast /or ovarian cancer | — |
ATM | ATM-related cancer susceptibility (ATM heterozygotes; see Ataxia-Telangiectasia.) | AD | Specific ATM pathogenic variants, most notably c.7271TG, are assoc w/high-penetrance breast cancer; heterozygosity for most other ATM pathogenic variants is assoc w/moderate-penetrance breast cancer. risk for other types of tumors such as pancreatic cancer prostate cancer. |
BARD1 | BARD1-related cancer susceptibility (OMIM 114480) | AD | Breast cancer |
BRIP1 | BRIP1-related cancer susceptibility (OMIM 605882) | AD | Epithelial ovarian cancer,3 possible risk for breast cancer CHEK2 |
susceptibility | AD | Breast cancer4 EPCAM MLH1 MSH2 MSH6 PMS2 | — |
Lynch syndrome | AD | Ovarian cancer, slightly risk for breast cancer. | — |
Source: GeneReviews — "BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer"