Presence of AR-V7 in Circulating Tumor Cells Validated as Predictive Biomarker for Advanced Prostate Cancer Treatment by Memorial Sloan Kettering and Epic Sciences
SAN DIEGO, June 4, 2016 /PRNewswire/ -- Detecting AR-V7 positive tumor cells circulating in the blood of an advanced prostate cancer patient predicts that he will not only fail the commonly-prescribed androgen receptor signaling inhibitors (ARSI), abiraterone and enzalutamide, but that he will survive significantly longer if treated with a taxane based chemotherapy regimen.
This discovery, published today in JAMA Oncology, emerged from a study of 161 progressing metastatic castration-resistant prostate cancer (mCRPC) patients about to start an FDA approved ARSIs or taxane as a first, second or third line treatment at Memorial Sloan Kettering Cancer Center (MSK). Blood samples taken along with those routinely collected from the patients were analyzed on the Epic Sciences' liquid biopsy platform for circulating tumor cells (CTCs) with the AR-V7 biomarker. Overall, almost 20% of patients had AR-V7 positive CTCs.
"The percentage of men that responds to ARSIs is highest in the first line setting, decreasing steadily as more treatments are given. We found that a novel liquid biopsy for AR-V7 was able to identify, with specificity, patients who will not benefit from these therapies and should instead start chemotherapy independent of the line of therapy being administered," said Howard Scher, M.D., chief of the genitourinary oncology services at MSK and corresponding author for the study.
Virtually all men with metastatic prostate cancer eventually develop mCRPC, an advanced state of the disease where the standard of care includes abiraterone, enzalutamide and taxanes. Although these therapies extend the lives of many men, approximately 20–25% of patients fail to respond in the first line, which increases to 60–70% in the second line setting. Worse is that determining non-response is often delayed, which may compromise the chance to benefit from alternative treatments.
A possible means for identifying non-responders emerged in 2014, when Johns Hopkins researchers discovered many patients' CTCs had the AR-V7 splice variant.
"We wanted to determine AR-V7's potential for guiding treatment decisions by assessing a real world sample from any mCRPC patient coming to Memorial Sloan Kettering Cancer Center," said Ryan Dittamore, co-investigator on the JAMA Oncology study and vice president of translational research and clinical affairs at Epic Sciences.
The researchers found that every AR-V7 positive patient identified by the Epic Sciences test failed to respond to abiraterone and enzalutamide, and experienced faster disease progression and shorter overall survival than AR-V7 negative patients. Additionally, patients who were AR-V7 positive survived longer when treated with taxane chemotherapies rather than abiraterone or enzalutamide (median 8.9 vs. 4.6 months). In multivariate models taking into account line of therapy and other critical clinical measures, patients who were AR-V7 positive had a 75.8% reduction of risk of death on taxane chemotherapy than on abiraterone or enzalutamide.
"This study indicates the potential for an AR-V7 predictive test to enable advanced prostate cancer patients to avoid ineffective therapies and to receive chemotherapy at an earlier stage when it may be more beneficial. Today no predictive diagnostic tests are available to improve treatment selection in prostate cancer—and they are urgently needed," said Murali Prahalad, Ph.D., CEO of Epic Sciences.
The Epic Sciences liquid biopsy platform used in the study images every nucleated cell in patients' blood to find those with the AR-V7 protein in the nucleus of all potential categories of CTCs, including non-traditional CTCs that are clustered or lack traditional protein markers such as cytokeratin (CK) or EpCAM. This allows identification, on a single cell basis, of rare subpopulations of metastatic cancer cells that may be resistant or susceptible to specific cancer therapies.
"Performing a liquid biopsy for AR-V7 on the Epic Sciences platform turned out to be advantageous from a clinical point of view for two key reasons. First, we could detect CTCs that might be missed with other detection methods, such as CK-negative cells, thereby improving our clinical sensitivity. Second, verifying the biomarker via nuclear-localized protein and not mRNA gives much greater confidence in the analytic specificity of the results, reinforced by the specificity of the clinical data in this study," explained Dittamore.
The study was funded by the National Institutes of Health and National Cancer Institute's Specialized Programs of Research Excellence and Cancer Center Support grants; the Department of Defense Prostate Cancer Research Program; the Prostate Cancer Foundation's Challenge Award; and the David H. Koch Fund for Prostate Cancer Research.
Reference: Scher, H et al. Association of AR-V7 on Circulating Tumor Cells as a Treatment-Specific Biomarker With Outcomes and Survival in Castration-Resistant Prostate Cancer. JAMA Oncology. Advance Online Publication: June 4, 2016. DOI:10.1001/jamaoncol.2016.1828
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.
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SOURCE Epic Sciences
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