Francesco Maura, MD, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, shares insights from his research utilizing whole genome sequencing (WGS) in patients with newly diagnosed multiple myeloma to elucidate the temporal sequence of genomic events. His investigation concludes that there are genomic deletions prior to the known initiating events of hyperdiploidy (HRD) and translocations affecting the immunoglobulin heavy chain (IGH) locus, which underly the inactivation of tumor suppressor genes. This interview took place at the 65th ASH Annual Meeting and Exposition, held in San Diego, CA.
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