<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liyasova M</submitter><funding>Molly and David Bloom Chair</funding><funding>Rapid Novor, Inc</funding><funding>Canadian Cancer Society Research Institute</funding><pagination>5028-5037</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9401514</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(18)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>M-protein is a well-established biomarker used for multiple myeloma monitoring. Current improvements in multiple myeloma treatment created the need to monitor minimal residual disease (MRD) with high sensitivity. Measuring residual levels of M-protein in serum by MS was established as a sensitive assay for disease monitoring. In this study we evaluated the performance of EasyM-a noninvasive, sensitive, MS-based assay for M-protein monitoring.&lt;h4>Experimental design&lt;/h4>Twenty-six patients enrolled in MCRN-001 clinical trial of two high-dose alkylating agents as conditioning followed by lenalidomide maintenance were selected for the study. All selected patients achieved complete responses (CR) during treatment, whereas five experienced progressive disease on study. The M-pro</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>A Personalized Mass Spectrometry-Based Assay to Monitor M-Protein in Patients with Multiple Myeloma (EasyM).</pubmed_title><pmcid>PMC9401514</pmcid><funding_grant_id>704269</funding_grant_id><pubmed_authors>Liyasova M</pubmed_authors><pubmed_authors>Piza G</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Trudel S</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Atenafu EG</pubmed_authors><pubmed_authors>Taylor P</pubmed_authors><pubmed_authors>Reece D</pubmed_authors><pubmed_authors>Ma B</pubmed_authors><pubmed_authors>McDonald Z</pubmed_authors><pubmed_authors>Gorospe K</pubmed_authors><pubmed_authors>Yao C</pubmed_authors><pubmed_authors>Xu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Personalized Mass Spectrometry-Based Assay to Monitor M-Protein in Patients with Multiple Myeloma (EasyM).</name><description>&lt;h4>Purpose&lt;/h4>M-protein is a well-established biomarker used for multiple myeloma monitoring. Current improvements in multiple myeloma treatment created the need to monitor minimal residual disease (MRD) with high sensitivity. Measuring residual levels of M-protein in serum by MS was established as a sensitive assay for disease monitoring. In this study we evaluated the performance of EasyM-a noninvasive, sensitive, MS-based assay for M-protein monitoring.&lt;h4>Experimental design&lt;/h4>Twenty-six patients enrolled in MCRN-001 clinical trial of two high-dose alkylating agents as conditioning followed by lenalidomide maintenance were selected for the study. All selected patients achieved complete responses (CR) during treatment, whereas five experienced progressive disease on study. The M-pro</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-05-10T06:44:17.571Z</modification><creation>2025-04-04T13:08:54.485Z</creation></dates><accession>S-EPMC9401514</accession><cross_references><pubmed>34210683</pubmed><doi>10.1158/1078-0432.CCR-21-0649</doi></cross_references></HashMap>