Ensartinib in resected ALK-positive non–small-cell lung cancer (Registro nro. 22732)

000 -Cabecera
Campo de control interno 02708nam a2200301 4500
001 - Número de control
control field ESSALUD
005 - Fecha y hora de la última transacción
Campo de control 20260804150724.0
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 Yue, Dongsheng
Rol del Autor Autor
9 (RLIN) 53711
245 ## - Titulo
Titulo Ensartinib in resected ALK-positive non–small-cell lung cancer
300 ## - Páginas
Paginación páginas: 151-161
520 ## - Resumen
Resumen Background: Anaplastic lymphoma kinase (ALK) inhibitors have emerged as promising agents for patients with resectable ALK-positive non–small-cell lung cancer (NSCLC). Whether ensartinib, a second-generation ALK inhibitor, is safe and effective in such patients is unknown. Methods: In this phase 3, double-blind, randomized trial involving patients with completely resected, ALK-positive stage IB to IIIB NSCLC after adjuvant chemotherapy, we randomly assigned patients in a 1:1 ratio to receive ensartinib at a dose of 225 mg once daily or placebo for 24 months. The primary end point was disease-free survival in patients with stage II to IIIB NSCLC. The key secondary end point was disease-free survival in the overall patient population. Results: A total of 274 patients were randomly assigned to receive ensartinib or placebo (137 patients in each group). At 24 months, the percentage of patients with stage II to IIIB disease who were alive and disease-free was 86.4% in the ensartinib group and 53.5% in the placebo group (hazard ratio for disease recurrence or death, 0.20; 95% confidence interval [CI], 0.11 to 0.38; P<0.001). In the overall patient population, the percentage of patients who were alive and disease-free was 87.3% in the ensartinib group and 57.2% in the placebo group (hazard ratio, 0.20; 95% CI, 0.10 to 0.37; P<0.001). Overall survival data were immature. Adverse events of grade 3 or higher occurred in 35.8% of the patients who received ensartinib (most commonly rash) and in 18.2% of those who received placebo. Conclusions: Among patients with completely resected stage IB to IIIB ALK-positive NSCLC, the percentage of patients who were alive and disease-free at 24 months was significantly higher with ensartinib than with placebo.<br/>
650 ## - Temas - Descriptores
Temas - Descriptores CANCER DE PULMÓN
9 (RLIN) 53712
650 ## - Temas - Descriptores
Temas - Descriptores NEUMOLOGÍA
9 (RLIN) 25628
650 ## - Temas - Descriptores
Temas - Descriptores CUIDADOS INTENSIVOS
9 (RLIN) 5208
650 ## - Temas - Descriptores
Temas - Descriptores TRATAMIENTO EN ONCOLOGÍA
9 (RLIN) 53713
700 ## - Autor Personal
Autor Personal Huang, Meijuan
9 (RLIN) 53714
700 ## - Autor Personal
Autor Personal Song, Pingping
9 (RLIN) 53715
700 ## - Autor Personal
Autor Personal Chen, Yuejun
9 (RLIN) 53716
700 ## - Autor Personal
Autor Personal Li, Bin
9 (RLIN) 53717
700 ## - Autor Personal
Autor Personal Fu, Junke
9 (RLIN) 53718
700 ## - Autor Personal
Autor Personal Guo, Jianji
9 (RLIN) 53719
773 0# - Revista (Relacion con el numero)
Host Biblionumber 22717
Host Itemnumber 22635
Ciudad, Editorial Massachusetts NEJM Group
Codigo barras item/ejemplar NEJM002
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 2026-07-30
Catalogador sqb

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