Lynch syndrome is the most common inherited cancer syndrome: a faulty mismatch-repair gene raises lifetime bowel cancer risk to 40-80% and also endometrial and other cancers.
Germline MLH1, MSH2, MSH6, PMS2, or EPCAM variants; ~3% of CRC and 1 in ~280 people. Colonoscopy every 1-2 years from age 20-25, aspirin chemoprevention (CAPP2), and risk-reducing hysterectomy. Lynch tumours are dMMR and highly immunotherapy-responsive; frameshift neoantigen vaccines (Nous-209) aim at prevention.
Showing the technology this term belongs to: Germline (hereditary) testing.
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.
Because Lynch syndrome tumours make the same abnormal proteins in almost every patient, a single vaccine could in principle be given to carriers before cancer develops. This small trial showed the concept is safe and immunogenic; whether it prevents cancer requires the randomised trials now being planned.
It is the second half of the argument for unselected germline testing, and it widens the target beyond BRCA: two thirds of the actionable inherited findings in prostate cancer are in other genes, including the mismatch repair genes that open a checkpoint inhibitor route.
It is the argument for sequencing every man with advanced prostate cancer rather than only the ones who look high risk: the phenotype is uncommon, it is invisible clinically, it opens the only durable immunotherapy route in this disease, and in one man in five it also identifies Lynch syndrome in the family.
The germline finding is the practical lesson: a meaningful minority of biliary cancer patients carry inherited repair-gene mutations that matter for PARP inhibitor eligibility and for their relatives, which argues for germline testing alongside tumour sequencing.
Guidelines recommending universal mismatch repair testing in pancreatic cancer, by immunohistochemistry or sequencing rather than PCR alone, rest on this and similar series.
It gives a cheap way to find the rare men who could benefit from checkpoint blockade: an immunohistochemical stain on the highest-grade primary tumours, where the yield is twenty times higher than average. It also shows the loss is clonal and early, so the diagnostic block is an adequate place to look.
The evidence that made germline testing standard for every man with metastatic prostate cancer, whatever his family history. It changes his treatment, because PARP inhibitors and platinum work better in these tumours, and it changes his relatives' screening, because BRCA2 carries breast, ovarian and pancreatic risk as well.
Shares CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer, Genomic characterization of biliary tract cancers identifies driver genes and predisposing mutations, Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma, MSH2 loss in primary prostate cancer.
Shares Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1, Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer, Genomic characterization of biliary tract cancers identifies driver genes and predisposing mutations, MSH2 loss in primary prostate cancer.
Shares CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer, Genomic characterization of biliary tract cancers identifies driver genes and predisposing mutations, Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma, Prevalence of germline variants in prostate cancer and implications for current genetic testing guidelines.
Shares Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer, MSH2 loss in primary prostate cancer, Hu 2018: evaluating mismatch repair deficiency in pancreatic adenocarcinoma, challenges and recommendations, Prevalence of microsatellite instability in prostate cancer and response to immune checkpoint blockade.
Shares Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer, Hu 2018: evaluating mismatch repair deficiency in pancreatic adenocarcinoma, challenges and recommendations, Prevalence of microsatellite instability in prostate cancer and response to immune checkpoint blockade, Identification of Lynch syndrome among patients with colorectal cancer.
Shares Inherited DNA-repair gene mutations in men with metastatic prostate cancer, Mismatch repair deficient (MSI-high) pancreatic ductal adenocarcinoma, Early-onset colorectal cancer (under 50), Germline vs somatic mutations.
Shares CAPP2: two years of aspirin cuts bowel cancer in Lynch syndrome by more than a third over 10 years, Aspirin for cancer prevention and adjuvant therapy, Chemoprevention & risk-reducing surgery, Inherited risk is mostly unidentified.
Shares Microsatellite-unstable (MSI-high) gastric cancer, MSI and mismatch-repair testing, Mismatch repair deficient (MSI-high) pancreatic ductal adenocarcinoma, Mismatch repair proteins (MLH1, MSH2, MSH6, PMS2).