SAN DIEGO, Nov. 16, 2016 /PRNewswire/ -- Epic Sciences announced findings demonstrating a circulating tumor cell (CTC)biomarker can identify patients with metastatic castrate resistant prostate cancer (mCRPC) who are more likely to respond to treatment with a PARP inhibitor in combination with androgen receptor signaling inhibitors (ARSi) compared to those treated with
At the 2016 ASCO Annual Meeting, this biomarker was reported by Epic Sciences to identify single HRD-positive (HRD+) CTCs. In addition, Epic Sciences demonstrated the clinical validity of this biomarker by prognosticating which mCRPC patients would have poor outcomes with ARSi and taxane chemotherapy.
Today, Epic reports on the further evaluation this biomarker as part of the NCI 9012 study to examine the efficacy of a PARP inhibitor (veliparib) in combination with an ARSi (abiraterone) in patients with mCRPC.
"PARP inhibitors are efficacious in a subset of patients with mCRPC. Therefore, it is critically important to find the patients who will benefit from these novel therapeutics," said Felix Feng, MD, associate professor of radiation oncology, urology and medicine at UCSF, and lead author of the study. "Identifying these patients with a simple blood draw represents a tremendous leap forward in the clinical development of PARP inhibitors."
The study demonstrated that 29 percent of first-line mCRPC patients were positive for the biomarker, while previous reports identify far fewer patients based on the detection of inactivating HRD mutations associated with PARP inhibitor response from sequencing of single-site, metastatic tissue biopsies (i.e. 13 percent of patients with BRCA2 loss).
In addition to observing increased prevalence within the cohort, the biomarker was used to observe and track dynamic changes in the HRD+ CTCs throughout a patient's treatment. On average, patients receiving the PARP inhibitor in conjunction with ARSi saw a reduction of HRD+ CTCs during therapy, whereas on average, patients given the ARSi alone saw an increase of HRD+ CTCs while on therapy.
"This circulating tumor cell biomarker clearly distinguishes a subset of patients who will have poor clinical response on ARSi alone but will have significantly improved responses with PARP inhibition. The biomarker's higher prevalence has been confirmed in multiple independent cohorts," said Ryan Dittamore, VP of translational research & clinical affairs at Epic Sciences and co-author on the study. "We are rapidly accelerating clinical development in partnership with biopharmaceutical companies and academic sponsors to evaluate the biomarker with many novel therapies including PARP inhibitors and other novel HRD-targeting therapies across a range of cancers."
About Epic Sciences
Epic Sciences, Inc. is developing novel diagnostics to personalize and advance the treatment and management of cancer. Epic Sciences' mission is to enable the rapid and non-invasive detection of genetic and molecular changes in cancer throughout a patient's journey. The company was founded on a powerful platform to identify and characterize rare cells, including circulating tumor cells (CTCs). Epic Sciences' no cell left behind® technology helps match patients to targeted therapies and monitor for drug resistance, so that the best treatment path can be chosen at every clinical decision point. Today, we partner with leading pharmaceutical companies and major cancer centers around the world. Epic Sciences' goal is to commercialize our technology to increase the success rate of cancer drugs in clinical trials and improve patient outcomes by providing physicians real-time information to guide treatment choices.
Further information is available on the Company's website, www.epicsciences.com. Stay in touch on Linkedin Epic Sciences, on Twitter @EpicSciences or on Facebook.com/EpicSciences.
To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/liquid-biopsy-biomarker-identifies-patients-with-improved-response-to-parp-inhibition-in-metastatic-castrate-resistant-prostate-cancer-300363620.html
SOURCE Epic Sciences
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