In contrast, none of the patients with nuclear localized AR-V7 protein expression in CTCs exhibited a response to ARSi, demonstrating superior performance of the nuclear localized approach. The difference between the scoring criteria also made significant differences in the prediction of therapeutic benefit of switching from commonly utilized ARSi to taxane chemotherapy, with only the nuclear scoring criteria demonstrating extension of life through switching therapies.
"The study results highlight the importance of robust analytic and clinical validation of predictive cancer biomarker tests at key clinical decision points in patient management," said Howard Scher, MD, chief of the genitourinary oncology service at MSK and lead author of the study. "The decision to prescribe intravenous treatment with a taxane over an oral ARSI needs to be based on a thoroughly evaluated technology in order to ensure patient outcomes are improved. Our work demonstrates the importance of the rigorous validation of the AR-V7 assay to guide the choice of systemic therapy in patients with metastatic disease."
The AR-V7 biomarker has been tested in multiple studies in CTCs and whole blood through detection of both AR-V7 protein and mRNA. While AR-V7 mRNA studies have demonstrated worse outcomes to ARSi, therapeutic responses to ARSi have been reported in AR-V7 mRNA positive patients.
"We know that when AR-V7 protein is detected in the nucleus of the tumor cell, those patients demonstrate high specificity to ARSi resistance," said Ryan Dittamore, vice president of translational research & clinical affairs, Epic Sciences and co-author on the study. "This study shows that using Epic Sciences' proprietary CTC platform to determine whether AR-V7 protein is sequestered in the cytoplasm or translocated to the nucleus can provide an important clinical difference compared to other technologies with less specific AR-V7 detection techniques."
In 2016, Epic Sciences partnered with Genomic Health, Inc., to offer the highly-specific nuclear AR-V7 liquid biopsy test later this year. Provided through Genomic Health's world-class Oncotype IQ Genomic Intelligence Platform and performed at the Epic Sciences CAP/CLIA-certified laboratory, the test is poised to address the needs of about 50,000 patients each year in the United States alone.
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, on Twitter @EpicSciences or on Facebook.com/EpicSciences.
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SOURCE Epic Sciences