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Overall survival benefits of first-line EGFR tyrosine kinase inhibitors in EGFR-mutated non-small-cell lung cancers: a systematic review and meta-analysis.
Kuan, Feng-Che; Kuo, Liang-Tseng; Chen, Min-Chi; Yang, Cheng-Ta; Shi, Chung-Sheng; Teng, David; Lee, Kuan-Der.
Afiliação
  • Kuan FC; Department of Hematology and Oncology, Chang-Gung Memorial Hospital, Chia-Yi 61363, Taiwan.
  • Kuo LT; Graduate Institute of Clinical Medical Sciences, Chang-Gung University, Tao-Yuan 33302, Taiwan.
  • Chen MC; Department of Orthopaedic Surgery, Division of Sports Medicine, Chang-Gung Memorial Hospital, Chia-Yi, Taiwan.
  • Yang CT; Centre for Evidence-Based Medicine, Chang-Gung Memorial Hospital, Chia-Yi, Taiwan.
  • Shi CS; Chang-Gung University of Science and Technology, Chia-Yi, Taiwan.
  • Teng D; Department of Public Health, Biostatistics Consulting Center, College of Medicine, Chang-Gung University, Tao-Yuan, Taiwan.
  • Lee KD; Department of Thoracic Medicine, Chang-Gung Memorial Hospital, Tao-Yuan 33305, Taiwan.
Br J Cancer ; 113(10): 1519-28, 2015 Nov 17.
Article em En | MEDLINE | ID: mdl-26461059
ABSTRACT

BACKGROUND:

Accumulating data shows that exon 19 deletions and L858R, both activating epidermal growth factor receptor mutations in non-small-cell lung cancers (NSCLCs), are just two different entities in terms of prognosis and treatment response to tyrosine kinase inhibitors (TKIs).

METHODS:

A systematic review and meta-analysis of randomized controlled trials comparing TKIs with conventional chemotherapy was performed. Eight trials of 1498 patients and five trials of 1279 patients with either exon 19 deletions or L858R were included in the meta-analysis.

RESULTS:

TKI treatment demonstrated progression-free survival benefit in patients with exon 19 deletions (hazard ratio (HR) 0.27, 95% confidence interval (CI) 0.21-0.35) and L858R (HR 0.45, 95% CI 0.35-0.58). Patients with exon 19 deletions had significant overall survival (OS) benefit under TKI treatment (HR 0.72, 95% CI 0.60-0.88). Subgroup analyses showed that irreversible TKIs, but not reversible TKIs, had statistically significant OS benefit in these patients (irreversible TKIs, HR 0.59, 95% CI 0.47-0.73; reversible TKIs, HR 0.84, 95% CI 0.69-1.02). Patients with L858R demonstrated no OS benefit under first-line TKI use (HR 1.15, 95% CI 0.95-1.39).

CONCLUSIONS:

In patients with advanced NSCLC harbouring exon 19 deletions, TKIs are associated with better OS compared with conventional chemotherapy. Future clinical trials should take exon 19 deletions and L858R as distinct disease entities and evaluate the treatment efficacy separately.
Assuntos

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Inibidores de Proteínas Quinases / Receptores ErbB / Neoplasias Pulmonares / Mutação Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Inibidores de Proteínas Quinases / Receptores ErbB / Neoplasias Pulmonares / Mutação Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article