Prognostic repair gene sequencing for prostate cancer patients (including BRCA)
Guidelines published in Jan 2018 suggest that physicians test their prostate cancer patients for germline mutations in BRCA and several other genes. The guidelines call for testing all patients with Gleason score (GS) 8, 9, 10 or metastatic (METS) disease (regardless of family history); and patients with Gleason score 6 or 7 with strong family history of cancer.1 The new NCCN guidelines stem from recent publications2 concluding that prostate cancer patients with those mutations may have more aggressive cancer, or develop 2nd primary cancers. And those with metastatic disease may be candidates for PARP inhibitors if mutations are present.
Prostate cancer patients with BRCA mutations…
…are more likely to develop metastatic disease.2
…are at risk of having or developing a 2nd primary cancer.2
…are candidates for PARP inhibitors (if disease is metastatic).2
…may have family members at risk of cancer.2
Patients with repair gene mutations should be considered for alternative management and treatment approaches.
BRCA testing is performed on the patient’s germline DNA. Strand uses buccal swabs already collected with the know error® system to obtain germline DNA samples sufficient to run its UroSeq™ Prostate Gene Panel test (BRCA1, BRCA2, ATM, CHEK2, PALB2 and RAD51D) in accordance with NCCN guidelines. Ordering UroSeq™ is fast and easy, there is no need to call the patient back to provide another specimen, nor a need to order a special kit. Since Strand routinely receives the Path reports with the order to test Know Error, we know the Gleason score from each patient and can determine from whom family history is needed (Gleason 6, 7) and for whom it’s not needed (Gleason 8, 9, 10, Mets). You can call to order the UroSeq™ panel testing or we can accept a standing, written reflex order that will allow us to proceed with testing automatically as appropriate for each patient. Fee free to contact us regarding any questions about the new guidelines or our test.
• Our testing platform is highly sensitive and specific
• Reports are tailored to urologists—only the relevant genes are reported
• Genetic counseling is provided for patients at no charge
• We are compliant with MolDx/CMS requirements to verify the source and purity of genomic test results.
1 Strong family history consists of: brother or father or multiple family members dx with PCa under 60yrs old; OR known germline repair gene mutations (e.g. BRCA2, LYNCH); OR more than one relative with breast, ovarian, pancreatic, colorectal, endometrial, gastric, kidney, small bowel, urothelial, bile duct cancer.
2 Pritchard CC1, Mateo J, et al; Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer. New England Journal of Medicine; 2016 Aug 4;375(5):443-53. doi: 10.1056/NEJMoa1603144.