Talquetamab–daratumumab in relapsed or refractory myeloma (Registro nro. 22827)

000 -Cabecera
Campo de control interno 03287nam a2200325 4500
001 - Número de control
control field ESSALUD
005 - Fecha y hora de la última transacción
Campo de control 20260817162604.0
007 - Tipo material - Descripcion fisica - info general
Tipo material - Descripcion fisica - info general ta
008 - Elementos de Longitud Fija - Información General
Elementos de Longitud Fija - Información t pe ||||| |||| 00| 0 spa d
040 ## - Origen de la Catalogación
Origen de la Catalogación BMG
041 ## - Idioma
Idioma eng
100 ## - Autor
Autor Mina, Roberto
Rol del Autor Autor
9 (RLIN) 53814
245 ## - Titulo
Titulo Talquetamab–daratumumab in relapsed or refractory myeloma
300 ## - Páginas
Paginación páginas: 671-683
520 ## - Resumen
Resumen Background: Talquetamab, a bispecific antibody targeting GPRC5D and CD3, has led to durable responses in patients with heavily pretreated relapsed or refractory multiple myeloma in phase 1–2 trials, with a limited effect on normal B cells. Methods: In a phase 3 trial, we randomly assigned patients with relapsed or refractory multiple myeloma who had previously received at least one line of therapy to receive talquetamab plus daratumumab and pomalidomide (Tal-DP), talquetamab plus daratumumab (Tal-D), or daratumumab plus pomalidomide and dexamethasone (DPd). The primary end point was progression-free survival as assessed by an independent review committee. Key secondary end points were overall response, complete response or better (complete or stringent complete response), measurable residual disease–negative complete response, and overall survival. Results: A total of 287, 287, and 290 patients were assigned to the Tal-DP, Tal-D, and DPd groups, respectively. At the interim analysis (median follow-up, 24.6 months), progression-free survival was significantly longer with Tal-DP and Tal-D than with DPd (24-month estimate, 81.3% and 77.6% vs. 51.2%; hazard ratio for disease progression or death, Tal-DP vs. DPd, 0.28 [95% confidence interval {CI}, 0.20 to 0.40], and Tal-D vs. DPd, 0.33 [95% CI, 0.24 to 0.46]; P<0.001 for both comparisons). The overall response was higher with Tal-DP and Tal-D than with DPd (88.2% and 88.5% vs. 77.6%), as was complete response or better (71.1% and 69.0% vs. 34.5%) and measurable residual disease–negative complete response (52.3% and 46.3% vs. 15.9%) (P<0.001 for all comparisons). Overall survival at 24 months was 89.2% with Tal-DP, 87.9% with Tal-D, and 79.1% with DPd (hazard ratio for death, Tal-DP vs. DPd, 0.47 [95% CI, 0.30 to 0.73], and Tal-D vs. DPd, 0.51 [95% CI, 0.33 to 0.78]). Serious adverse events occurred in 63.0%, 52.6%, and 53.7% of the patients in the Tal-DP, Tal-D, and DPd groups, respectively; fatal adverse events occurred in 1.8%, 4.0%, and 4.6%. Conclusions: Among patients with relapsed or refractory multiple myeloma who had previously received at least one line of therapy, both Tal-DP and Tal-D led to significantly longer progression-free survival than DPd.
650 ## - Temas - Descriptores
Temas - Descriptores LEUCEMIA
9 (RLIN) 33873
650 ## - Temas - Descriptores
Temas - Descriptores LINFOMA
9 (RLIN) 39360
650 ## - Temas - Descriptores
Temas - Descriptores CUIDADOS INTENSIVOS GENERAL
9 (RLIN) 54115
650 ## - Temas - Descriptores
Temas - Descriptores TRATAMIENTOS EN ONCOLOGÍA
9 (RLIN) 53734
700 ## - Autor Personal
Autor Personal Beksac, Meral
9 (RLIN) 54122
700 ## - Autor Personal
Autor Personal Rodríguez-Otero, Paula
9 (RLIN) 54123
700 ## - Autor Personal
Autor Personal Chen,Wenming
9 (RLIN) 53818
700 ## - Autor Personal
Autor Personal Mateos, María-Victoria
9 (RLIN) 54124
700 ## - Autor Personal
Autor Personal Li, Jian
9 (RLIN) 54125
700 ## - Autor Personal
Autor Personal Moreau, Philippe
9 (RLIN) 54126
700 ## - Autor Personal
Autor Personal Cohen, Yael C.
9 (RLIN) 54127
700 ## - Autor Personal
Autor Personal Min, Chang-Ki
9 (RLIN) 54128
773 0# - Revista (Relacion con el numero)
Host Biblionumber 22717
Host Itemnumber 22647
Ciudad, Editorial Massachusetts NEJM Group
Codigo barras item/ejemplar NEJM010
Titulo de la Revista The New England Journal of Medicine
Número de control de registro ESSALUD
ISSN 0028-4793
942 ## - Elementos de Koha
Tipo de Documento Artículos
Fecha procesamiento 2026-08-17
Catalogador SQB

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