Project aims to standardize MRD data generation, assessment and accelerate AML clinical trial programs bringing novel therapies to patients in need faster
SAN FRANCISCO, Jan. 14, 2021 /PRNewswire/ — Invitae Corporation (NYSE: NVTA), a leading medical genetics company, today announced the launch of a new project with Bristol Myers Squibb, Janssen Research & Development, LLC (Janssen), Novartis and Genentech, a member of the Roche Group, to develop a standardized panel for MRD detection in patients with AML to support clinical trial testing across multiple drug development programs. The companies are working together to standardize how MRD data is generated and assessed in clinical trials helping to better establish the clinical utility of MRD as a biomarker in AML.
“Given the existing evidence that shows assessing the presence of MRD can provide valuable information on how well a treatment may be working, we hope to further establish MRD detection as an objective tool for clinicians to create the best treatment plan for individual patients,” said Jason Myers, Ph.D., president of oncology at Invitae. “Together with leading, global biopharmaceutical companies, Bristol Myers Squibb, Janssen, Novartis and Genentech, we intend to develop a panel that can accurately measure and standardize MRD data collection in clinical trials with the goal of accelerating trial timeframes to bring novel therapies to patients in need sooner.”
MRD is the detection of residual disease after treatment based on the presence of molecular biomarkers when the remaining cancer cells are not detectable by conventional methods. The detection of MRD typically relies on highly sensitive and specific technologies such as next-generation sequencing, which has become more commonly used in recent years. Specifically, in AML and other blood cancers, studies have shown the presence of MRD after treatment may predict survival outcomes for patients.
While a growing body of evidence continues to demonstrate a correlation between MRD and the risk of disease relapse or recurrence among other prognostic factors, lack of standardization of MRD technologies and assessment methods have slowed the acceptance of MRD as a clinical trial endpoint in AML. Another goal of the project is to further evaluate MRD as a predictive biomarker and clinical trial endpoint to assess the effectiveness of novel therapies.
“We’re proud to be working with these leading companies to further refine the standards for MRD detection and help establish its utility as an accurate and rapid indicator of treatment effect,” said Sean George, Ph.D., co-founder and chief executive officer of Invitae. “Standardized MRD results can help give providers confidence they are creating a personalized plan for their patients with the goal of improving quality of life and overall survival.”
The multi-gene, next-generation sequencing panel is expected to be used in AML clinical trials to measure baseline molecular status as well as track MRD status. The panel will be built on Invitae’s Anchored Multiplex PCR (AMP™) chemistry, allowing the tests to be completed in laboratories at local clinical trial testing sites across the globe, reducing turnaround time for results.
Approximately 50%-60% of de novo AML and 80%-90% of secondary AML patients have genetic alterations. The comprehensive next-generation sequencing panel is being designed to detect more than 90% of the genetic alterations associated with AML, including key molecular targets CEBPA, FLT3, IDH1 and IDH2.
Author / source: Invitae / https://ir.invitae.com/news-and-events/press-releases/press-release-details/2021/Leading-Biopharmaceutical-Companies-Select-Invitae-to-Develop-Standardized-Panel-to-Detect-Molecular-Residual-Disease-MRD-in-Patients-with-Acute-Myeloid-Leukemia-AML/default.aspx