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    510(k) clearance will allow 23andMe to report an additional 41 genetic variants in the BRCA1 and BRCA2 genes that increase risk for breast, ovarian, prostate and pancreatic cancer Many of these additional variants occur more often in people of African American and Hispanic/Latino descent 23andMe also granted an FDA Predetermined Change Control Plan, allowing the company to update its BRCA report with additional variants without a pre-market submission, provided those variants meet the same rigor

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    • RT @westr: @23andMe Granted New FDA Clearance to Report Additional #BRCA Variants https://t.co/WW3V8kX4Zf via @YahooFinance "will allow #…

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    AbstractGermline BRCA–associated pancreatic ductal adenocarcinoma (glBRCA PDAC) tumors are susceptible to platinum and PARP inhibition. The clinical outcomes of 125 patients with glBRCA PDAC were stratified based on the spectrum of response to platinum/PARP inhibition: (i) refractory [overall survival (OS) <6 months], (ii) durable response followed by acquired resistance (OS <36 months), and (iii) long-term responders (OS >36 months). Patient-derived xenografts (PDX) were generated from 25 patients with glBRCA PDAC at different clinical time points. Response to platinum/PARP inhibition in vivo and ex vivo culture (EVOC) correlated with clinical response. We deciphered the mechanisms of resistance in glBRCA PDAC and identified homologous recombination (HR) proficiency and secondary mutations restoring partial functionality as the most dominant resistant mechanism. Yet, a subset of HR-deficient (HRD) patients demonstrated clinical resistance. Their tumors displayed basal-like molecular s

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    • #ICYMI— Spectrum of Response to Platinum and #PARP Inhibitors in Germline #BRCA–Associated #PancreaticCancer in the Clinical and Preclinical Setting, by @ChaniStossel, Maria Raitses-Gurevich Talia Golan et al. https://t.co/dKqtorhfSw @sheba_medical @TelAvivUni https://t.co/c1x9hjKqug

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    Photo: Luke Henry, the ICRWe demonstrated that drugs called PARP inhibitors could be particularly effective in BRCA-mutant cancers and, with The Royal Marsden NHS Foundation Trust, helped run clinical trials leading to the first PARP inhibitor being licensed in ovarian cancer. The PARP inhibitor story began back in the mid-1990s, when a team of researchers at The Institute of Cancer Research –…

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    • 🔬🧬We previously applied genetic principles to discover a novel strategy for #Cancer treatment for patients with #BRCA 1/2 mutations. Read more about the ICR’s role in the science that underpins the olaparib discovery: https://t.co/8W5SOcdjIx