Germline (hereditary) testing
A test of the DNA you were born with, to find inherited risk genes such as BRCA or Lynch syndrome.
Multi-gene hereditary panels (BRCA1/2, PALB2, TP53, Lynch genes, CDH1, ATM, CHEK2) are recommended for all TNBC, ovarian, pancreatic, and metastatic prostate cancer patients and increasingly for all breast cancer. Findings change surgery, drug choice (PARP inhibitors), and family screening.
How it works
NGS of blood or saliva DNA identifies pathogenic germline variants.
- Actionable for patient and relatives
- Cheap
- VUS burden
- Uptake and counselling capacity
Everyone with HER2-negative early breast cancer that meets high-risk criteria should be offered germline BRCA testing, because a positive result now changes treatment: a year of olaparib after chemotherapy reduces relapse and death. It does not apply to low-risk tumours, HER2-positive disease, or somatic-only BRCA mutations.
People with Lynch syndrome should be offered daily aspirin, which roughly halves bowel cancer risk with a delayed and durable effect. Whether a lower dose (as tested in CAPP3) is as effective, and whether the finding extends to the general population, are separate questions.
Every woman diagnosed with advanced high-grade ovarian cancer should be tested for BRCA mutations at diagnosis, because those who carry one should receive two years of olaparib after chemotherapy, which greatly extends the time in remission and improves long-term survival. The plateau in the survival curves suggests some patients are cured by this approach. Toxicity is mostly anaemia, fatigue and nausea, and the two-year limit appears sufficient.
For women who carry a BRCA mutation, preventive removal of the ovaries and tubes saves lives, and preventive mastectomy almost eliminates breast cancer. These are the strongest prevention effects in oncology, which is why finding carriers before they develop cancer matters so much.
Latest papers
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