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dc.contributor.authorMateos, María-Victoriaes_ES
dc.contributor.authorWeisel, Katjaes_ES
dc.contributor.authorDe Stefano, Valerioes_ES
dc.contributor.authorGoldschmidt, Hartmutes_ES
dc.contributor.authorDelforge, Micheles_ES
dc.contributor.authorMohty, Mohamades_ES
dc.contributor.authorDytfeld, Dominikes_ES
dc.contributor.authorAngelucci, Emanuelees_ES
dc.contributor.authorVincent, Laurees_ES
dc.contributor.authorPerrot, Aurorees_ES
dc.contributor.authorBenjamin, Reubenes_ES
dc.contributor.authorVan de Donk, Niels W. C. J.es_ES
dc.contributor.authorOcio San Miguel, Enrique María es_ES
dc.contributor.authorRoccia, Titoes_ES
dc.contributor.authorSchecter, Jordan M.es_ES
dc.contributor.authorKoskinen, Silvaes_ES
dc.contributor.authorHaddad, Imènees_ES
dc.contributor.authorStrulev, Vadimes_ES
dc.contributor.authorMitchell, Ladaes_ES
dc.contributor.authorBuyze, Jozefienes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-03-10T10:52:47Z
dc.date.available2025-03-10T10:52:47Z
dc.date.issued2024es_ES
dc.identifier.issn0887-6924es_ES
dc.identifier.issn1476-5551es_ES
dc.identifier.urihttps://hdl.handle.net/10902/35928
dc.description.abstractTreatment of relapsed/refractory multiple myeloma (RRMM) is challenging as patients exhaust all available therapies and the disease becomes refractory to standard drug classes. Here we report the final results of LocoMMotion, the first prospective study of real-world clinical practice (RWCP) in triple-class exposed (TCE) patients with RRMM, with a median follow-up of 26.4 months (range, 0.1-35.0). Patients (N = 248) had received median 4 prior LOT (range, 2-13) at enrollment. 91 unique regimens were used in index LOT. Overall response rate was 31.9% (95% CI, 26.1-38.0), median progression-free survival (PFS) was 4.6 months (95% CI, 3.9-5.6) and median overall survival was 13.8 months (95% CI, 10.8-17.0). 152 patients (61.3%) had subsequent LOTs with 134 unique regimens, of which 78 were used in first subsequent LOT. Median PFS2 (from start of study through first subsequent LOT) was 10.8 months (95% CI, 8.4-13.0). 158 patients died on study, 67.7% due to progressive disease. Additional subgroup analyses and long-term safety summaries are reported. The high number of RWCP treatment regimens utilized and poor clinical outcomes confirm a lack of standardized treatment for TCE patients with RRMM, highlighting the need for new treatments with novel mechanisms.es_ES
dc.description.sponsorshipThis study (ClinicalTrials.gov identifier: NCT04035226) was funded by Janssen Research & Development, LLC and Legend Biotech USA Inc. Medical writing support was provided by Andrew Marson and Sarika Pathak Sharma, PhD, of Eloquent Scientific Solutions, and funded by Janssen Global Services, LLC. The authors thank the LocoMMotion study team, including Jonathan Squire, Kensa Hatch, Lorenzo Acciarri, Henrieke Bruin, and Jeannie Kearl.es_ES
dc.format.extent7 p.es_ES
dc.language.isoenges_ES
dc.publisherNature Publishing Groupes_ES
dc.rights© The Author(s) 2024. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceLeukemia, 2024, 38, 2554-2560es_ES
dc.titleLocoMMotion: a study of real-life current standards of care in triple-class exposed patients with relapsed/refractory multiple myeloma - 2-year follow-up (final analysis)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1038/s41375-024-02404-6es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1038/s41375-024-02404-6es_ES
dc.type.versionpublishedVersiones_ES


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© The Author(s) 2024. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holderExcepto si se señala otra cosa, la licencia del ítem se describe como © The Author(s) 2024. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder