<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zabaleta A</submitter><funding>La Caixa Foundation</funding><funding>Cancer Research UK (A26819), FCAECC and AIRC under the Accelerator Award Programme (EDITOR)</funding><funding>Instituto de Salud Carlos III</funding><funding>Riney Family Multiple Myeloma Research Program</funding><funding>Instituto de Salud Carlos III/Subdirección General de Investigación Sanitaria, (cofunded by the EU)</funding><funding>Black Swan Research Initiative of the International Myeloma Foundation</funding><funding>Fundación Científica Asociación Española Contra el Cáncer</funding><funding>CIBER-Consorcio Centro de Investigación Biomédica en Red - Área de Oncología - Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación</funding><funding>CRIS Cancer Foundation</funding><pagination>93-102</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11625977</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>100(1)</volume><pubmed_abstract>The impact of measurable residual disease (MRD) in relapse/refractory multiple myeloma (RRMM) patients treated with T-cell redirecting immunotherapy is uncertain. We analyzed MRD dynamics using next-generation flow in 201 patients treated in clinical trials with chimeric antigen receptor (CAR) T cells and T-cell engagers (TCE). Achieving MRD negativity at 10&lt;sup>-6&lt;/sup> was associated with 89% reduction in the risk of progression and/or death. Survival outcomes were improved in patients with sustained versus transient MRD negativity and were dismal in those who remained MRD positive. The intent-to-treat MRD negative rates were higher in patients treated with CAR T cells versus TCE. However, among patients achieving MRD negativity, there were no differences in survival outcomes when strati</pubmed_abstract><journal>American journal of hematology</journal><pubmed_title>Clinical significance of complete remission and measurable residual disease in relapsed/refractory multiple myeloma patients treated with T-cell redirecting immunotherapy.</pubmed_title><pmcid>PMC11625977</pmcid><funding_grant_id>PR_EX_2020‐02</funding_grant_id><funding_grant_id>PI19/01451</funding_grant_id><funding_grant_id>CB16/12/00233</funding_grant_id><funding_grant_id>ICI19/00025</funding_grant_id><funding_grant_id>PI21/01816</funding_grant_id><funding_grant_id>CP042702/LCF/PR/GN18/50310007</funding_grant_id><funding_grant_id>CB16/12/00369</funding_grant_id><funding_grant_id>CB16/12/00489</funding_grant_id><funding_grant_id>PI22/00647</funding_grant_id><funding_grant_id>PR_EX_2020-02</funding_grant_id><pubmed_authors>Moreno C</pubmed_authors><pubmed_authors>Mateos MV</pubmed_authors><pubmed_authors>Puertas B</pubmed_authors><pubmed_authors>Zabaleta A</pubmed_authors><pubmed_authors>Blade J</pubmed_authors><pubmed_authors>Lopez-Corral L</pubmed_authors><pubmed_authors>Urbano A</pubmed_authors><pubmed_authors>Cedena MT</pubmed_authors><pubmed_authors>Puig N</pubmed_authors><pubmed_authors>Tamariz-Amador LE</pubmed_authors><pubmed_authors>Lopez-Munoz N</pubmed_authors><pubmed_authors>Rey-Bua B</pubmed_authors><pubmed_authors>Martinez-Lopez J</pubmed_authors><pubmed_authors>Juan M</pubmed_authors><pubmed_authors>de Larrea CF</pubmed_authors><pubmed_authors>Rodriguez-Otero P</pubmed_authors><pubmed_authors>Perez JJ</pubmed_authors><pubmed_authors>Prosper F</pubmed_authors><pubmed_authors>Miras F</pubmed_authors><pubmed_authors>Paiva B</pubmed_authors><pubmed_authors>Gonzalez-Calle V</pubmed_authors><pubmed_authors>San Miguel JF</pubmed_authors><pubmed_authors>Gonzalez-Navarro EA</pubmed_authors><pubmed_authors>Lahuerta JJ</pubmed_authors><pubmed_authors>Sanchez-Pina JM</pubmed_authors><pubmed_authors>Oliver-Caldes A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical significance of complete remission and measurable residual disease in relapsed/refractory multiple myeloma patients treated with T-cell redirecting immunotherapy.</name><description>The impact of measurable residual disease (MRD) in relapse/refractory multiple myeloma (RRMM) patients treated with T-cell redirecting immunotherapy is uncertain. We analyzed MRD dynamics using next-generation flow in 201 patients treated in clinical trials with chimeric antigen receptor (CAR) T cells and T-cell engagers (TCE). Achieving MRD negativity at 10&lt;sup>-6&lt;/sup> was associated with 89% reduction in the risk of progression and/or death. Survival outcomes were improved in patients with sustained versus transient MRD negativity and were dismal in those who remained MRD positive. The intent-to-treat MRD negative rates were higher in patients treated with CAR T cells versus TCE. However, among patients achieving MRD negativity, there were no differences in survival outcomes when strati</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-18T13:09:40.281Z</modification><creation>2025-04-06T22:42:27.548Z</creation></dates><accession>S-EPMC11625977</accession><cross_references><pubmed>39548827</pubmed><doi>10.1002/ajh.27526</doi></cross_references></HashMap>