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EGFR-Tyrosine Kinase Inhibitor Retreatment in Non-Small-Cell Lung Cancer Patients Previously Exposed to EGFR-TKI: A Systematic Review and Meta-Analysis.
Michelon, Isabella; Vilbert, Maysa; do Rego Castro, Caio Ernesto; Stecca, Carlos; Dacoregio, Maria Inez; Rizzo, Manglio; Cláudio Cordeiro de Lima, Vladmir; Cavalcante, Ludimila.
Afiliación
  • Michelon I; Department of Medicine, Catholic University of Pelotas, Pelotas 96015-560, Brazil.
  • Vilbert M; Massachusetts General Hospital Cancer Center, Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
  • do Rego Castro CE; Department of Medicine, University of Brasilia, Brasília 70910-900, Brazil.
  • Stecca C; Department of Medicine, Parana Oncology Center, Curitiba 80030-200, Brazil.
  • Dacoregio MI; Department of Medicine, University of Centro Oeste, Guarapuava 85040-167, Brazil.
  • Rizzo M; Cancer Immunobiology Laboratory, Instituto de Investigaciones en Medicina Traslacional, Universidad Austral-Consejo Nacional de Investigaciones Cientificas y Tecnologicas (CONICET), Buenos Aires 1428, Argentina.
  • Cláudio Cordeiro de Lima V; Clinical Oncology Unit, Hospital Universitario Austral, Av. Presidente Perón 1500, (B1629ODT) Derqui-Pilar, Buenos Aires 1428, Argentina.
  • Cavalcante L; Department of Medical Oncology, AC Camargo Cancer Center, São Paulo 01509-010, Brazil.
J Pers Med ; 14(7)2024 Jul 15.
Article en En | MEDLINE | ID: mdl-39064005
ABSTRACT
We performed a systematic review and meta-analysis to assess the efficacy of EGFR-tyrosine kinase inhibitors (TKI) retreatment in advanced/metastatic non-small-cell lung cancer (NSCLC) patients. We systematically searched PubMed, Embase, Cochrane databases, ASCO, and ESMO websites for studies evaluating EGFR-TKI retreatment in advanced/metastatic NSCLC patients. All analyses were performed using R software (v.4.2.2). We included 19 studies (9 CTs and 10 retrospective cohorts) with a total of 886 patients. In a pooled analysis of all patients during retreatment with TKI, median OS was 11.7 months (95% confidence interval [CI] 10.2-13.4 months) and PFS was 3.2 months (95% CI 2.5-3.9 months). ORR was 15% (95% CI 10-21%) and DCR was 61% (95% CI 53-67%). The subanalysis by generation of TKI in the rechallenge period revealed a slightly better ORR for patients on 3rd generation TKI (p = 0.05). Some limitations include the high heterogeneity of some of the analyses and inability to perform certain subanalyses. Our results unequivocally support the benefit of EGFR-TKI rechallenge in EGFR-mutated NSCLC patients progressing on TKI treatment after a TKI-free interval. These findings may be especially valuable in areas where access to novel therapeutic drugs and clinical trials is limited.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Pers Med Año: 2024 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Pers Med Año: 2024 Tipo del documento: Article País de afiliación: Brasil
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