<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>104(3)</volume><submitter>Costa LJ</submitter><funding>Amgen</funding><pubmed_abstract>Although survival rates for patients with newly diagnosed multiple myeloma (NDMM) have improved over recent decades, multiple myeloma (MM) remains without a cure for most. There is increasing consensus that achievement of deep remissions, especially minimal residual disease negativity (MRD -), in frontline treatment is crucial and translates into improved survival. The standard of care (SOC) for NDMM consists at minimum of a triplet regimen of therapies, with or without an autologous stem cell transplant, or a doublet regimen for certain ineligible, particularly frail patients who may have specific limitations. Recently, anti-CD38 monoclonal antibodies (mAbs), such as daratumumab (Dara) or isatuximab (Isa), have been integrated into frontline SOC regimens. Seeking to further deepen and pro</pubmed_abstract><journal>Annals of hematology</journal><pagination>1329-1351</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12031813</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Evolution of frontline treatment for multiple myeloma: clinical investigation of quadruplets containing carfilzomib and anti-CD38 monoclonal antibodies.</pubmed_title><pmcid>PMC12031813</pmcid><pubmed_authors>Touzeau C</pubmed_authors><pubmed_authors>McFadden I</pubmed_authors><pubmed_authors>Gay F</pubmed_authors><pubmed_authors>Costa LJ</pubmed_authors><pubmed_authors>Mateos MV</pubmed_authors><pubmed_authors>Weisel K</pubmed_authors><pubmed_authors>Moreau P</pubmed_authors><pubmed_authors>Landgren O</pubmed_authors><pubmed_authors>Ertel F</pubmed_authors><pubmed_authors>Najdi R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evolution of frontline treatment for multiple myeloma: clinical investigation of quadruplets containing carfilzomib and anti-CD38 monoclonal antibodies.</name><description>Although survival rates for patients with newly diagnosed multiple myeloma (NDMM) have improved over recent decades, multiple myeloma (MM) remains without a cure for most. There is increasing consensus that achievement of deep remissions, especially minimal residual disease negativity (MRD -), in frontline treatment is crucial and translates into improved survival. The standard of care (SOC) for NDMM consists at minimum of a triplet regimen of therapies, with or without an autologous stem cell transplant, or a doublet regimen for certain ineligible, particularly frail patients who may have specific limitations. Recently, anti-CD38 monoclonal antibodies (mAbs), such as daratumumab (Dara) or isatuximab (Isa), have been integrated into frontline SOC regimens. Seeking to further deepen and pro</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-02T20:38:50.957Z</modification><creation>2025-07-11T03:04:02.236Z</creation></dates><accession>S-EPMC12031813</accession><cross_references><pubmed>39774926</pubmed><doi>10.1007/s00277-024-06143-7</doi></cross_references></HashMap>