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TREATMENT PATTERNS AND OUTCOMES IN THE SECOND AND THIRD LINES AND AFTER TRIPLE-CLASS EXPOSURE: SUBANALYSIS OF THE LATIN AMERICAN MULTIPLE MYELOMA REGISTRY STUDY (MYLACRE)

dc.contributor.authorMaiolino, A
dc.contributor.authorGalvez, K
dc.contributor.authorRemaggi, G
dc.contributor.authorSchutz, N
dc.contributor.authorBittencourt, R
dc.contributor.authorHungria, V
dc.contributor.authorColaco, C
dc.contributor.authorCrusoe, E
dc.contributor.authorTobias, W
dc.contributor.authorGaiolla, R [UNESP]
dc.date.accessioned2026-07-14T17:49:30Z
dc.date.issued2025-10-01
dc.description.abstractIntroduction Patterns of care for multiple myeloma (MM) vary across countries. MYLACRE was a non-interventional registry of patients (pts) diagnosed with MM between in Latin America. We analyzed MYLACRE pts treated in the 2nd and 3rd lines of therapy (LOT2 and LOT3), with the objective of characterizing treatment (tx) patterns. We also investigated tx strategies and outcomes in the subset of triple-class exposed (TCE) pts. Objectives Characterizing treatment (tx) patterns. We also investigated tx strategies and outcomes in the subset of triple-class exposed (TCE) pts. Material and methods Data were retrospectively collected, and tx was left to investigators’ discretion. The LOT2 Population comprised all pts who had an entry for the start date of LOT2. The LOT3 Population comprised all pts from the LOT2 Population who had an entry of the start date of LOT3. We defined TCE pts as those who had received ≥1 proteasome inhibitor (PI), ≥1 immunomodulatory drug (IMiD), and ≥1 anti-CD38 antibody, regardless of tx duration. We analyzed TCE pts with at least one subsequent LOT after becoming TCE. We analyzed time to next treatment (TTNT) and overall survival (OS), with TTNT measured between Day 1 of the LOT of interest and Day 1 of the subsequent LOT. Resultados Of the 1029 pts originally analyzed, 405 and 167 entered the LOT2 and LOT3 Populations, respectively. In LOT2, the most frequently used PI, IMiD, and anti- CD38 were bortezomib (41.0%), lenalidomide (41.0%) and daratumumab (26.2%). Other agents used in >10% were carfilzomib (17.0%) and thalidomide (19.3%). The median TTNT was 21.2 months (mo), and median OS was 26.1 mo. In LOT3, Carfilzomib (26.9%), Lenalidomide (34.7%), and Daratumumab (18.6%) were, respectively, the most common PI, IMiD, and anti-CD38. Bortezomib (25.7%) and thalidomide (10.8%) were the next most frequent. The median TTNT was 12.2 mo, median OS was 14.5 mo. A total of 166 (16.1%) pts had a record of tx with ≥1 PI, ≥1 IMiD, and ≥1 anti-CD38 at some point. Of these pts, 48 (48/166=28.9%) initiated a subsequent LOT after TCE and entered the TCE Population. These pts became TCE after LOT1 (n = 5), LOT2 (n = 27), LOT3 (n = 8), or later (n = 8). Considering agents belonging to the PI, IMID, and anti-CD38 classes, Carfilzomib was the agent most frequently used in the first LOT after TCE (52.1%), followed by Lenalidomide (22.9%), pomalidomide (20.8%), Daratumumab (18.8%), and Thalidomide (10.4%). Forty-five TCE pts could be analyzed for TTNT and OS. The median TTNT was 9.5 mo (95% CI, 5.9 to 19.4 mo). The median OS was 13.4 mo (95% CI, 10.6 to 17.7 mo). Discussion and conclusion This snapshot of pts with MM treated in Latin America shows heterogeneity in txs used in LOT2, LOT3, and after TCE status, suggesting a lack of standard of care in the real world. The difference between real-life drug use and international guidelines could also be determined by access barriers. The short OS, especially after TCE, highlights the importance of more effective tx options to improve outcomes. Funding This study was funded by Johnson & Johnson and Legend Biotech USA In.
dc.description.affiliationClínicas Oncológicas lntegradas, Rio de Janeiro, Brazil
dc.description.affiliationHospital Pablo Tobon Uribe, Medellín, Colombia
dc.description.affiliationFundaleu, Buenos Aires, Argentina
dc.description.affiliationHospital Italiano de Buenos Aires, Buenos Aires, Argentina
dc.description.affiliationHospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Brazil
dc.description.affiliationClinica Sao Germano, São Paulo, Brazil
dc.description.affiliationLiga Contra o Cancer, Natal, Brazil; Fundacion Santa Fe de Bogota, Colombia
dc.description.affiliationlnstituto D'or Oncologia, Salvador, Brazil
dc.description.affiliationHospital São Paulo, São Paulo, Brazil
dc.description.affiliationFaculdade de Medicina de Botucatu, Universidade Estadual Paulista (UNESP), Botucatu, Brazil
dc.description.affiliationUnespFaculdade de Medicina de Botucatu, Universidade Estadual Paulista (UNESP), Botucatu, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1194408806
dc.identifier.dimensionspub.1194408806
dc.identifier.doi10.1016/j.htct.2025.104869
dc.identifier.issn2531-1379
dc.identifier.issn2531-1387
dc.identifier.orcid0000-0003-0140-9548
dc.identifier.orcid0000-0002-6320-8867
dc.identifier.orcid0000-0002-1167-7186
dc.identifier.orcid0000-0002-3173-4141
dc.identifier.orcid0000-0002-4327-1957
dc.identifier.orcid0000-0002-9480-4995
dc.identifier.urihttps://hdl.handle.net/11449/327683
dc.publisherElsevier
dc.relation.ispartofHematology Transfusion and Cell Therapy; v. 47; p. 104869
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
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dc.titleTREATMENT PATTERNS AND OUTCOMES IN THE SECOND AND THIRD LINES AND AFTER TRIPLE-CLASS EXPOSURE: SUBANALYSIS OF THE LATIN AMERICAN MULTIPLE MYELOMA REGISTRY STUDY (MYLACRE)
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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