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| Elisabet Manasanch, M.D. | Linghua Wang, M.D., Ph.D. Photo Credit: Courtesy of University of Texas MD Anderson Cancer Center |
A new study by researchers at The University of Texas MD Anderson Cancer Center highlights novel insights into the evolution of multiple myeloma from precursor disease, which may help better identify patients likely to progress and develop new interventions.
Published today in Cancer Cell, the study integrates paired single-cell RNA sequencing and B cell receptor sequencing from 64 patients with multiple myeloma or precursor disease. The study achieved several notable milestones in the effort to better understand this evolutionary process and is believed to be the largest cohort of myeloma precursor patient samples analyzed at single-cell resolution.
How multiple myeloma, a deadly and incurable cancer of plasma cells in the bone marrow, evolves from precursor conditions like monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma remains largely a mystery. To help solve that mystery, this study was designed by Elisabet Manasanch, M.D., associate professor of Lymphoma/Myeloma, in collaboration with Linghua Wang, M.D., Ph.D., associate professor of Genomic Medicine, and Minghao Dang, Ph.D., postdoctoral fellow in the Wang lab.
“This research is a big step towards understanding the evolutionary roadmap that leads to myeloma,” Wang said. “Additionally, there is a significant clinical unmet need to find and validate novel biomarkers to identify patients at high-risk of progression who would benefit the most from early treatment interventions.”





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