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Neoadjuvant Chemoimmunotherapy for NSCLC: A Systematic Review and Meta-Analysis.
Sorin, Mark; Prosty, Connor; Ghaleb, Louis; Nie, Kathy; Katergi, Khaled; Shahzad, Muhammad H; Dubé, Laurie-Rose; Atallah, Aline; Swaby, Anikka; Dankner, Matthew; Crump, Trafford; Walsh, Logan A; Fiset, Pierre O; Sepesi, Boris; Forde, Patrick M; Cascone, Tina; Provencio, Mariano; Spicer, Jonathan D.
Afiliação
  • Sorin M; Rosalind and Morris Goodman Cancer Institute, McGill University, Montréal, Quebec, Canada.
  • Prosty C; Department of Human Genetics, McGill University, Montréal, Quebec, Canada.
  • Ghaleb L; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Nie K; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Katergi K; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Shahzad MH; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Dubé LR; Faculty of Medicine, University of Montreal, Montréal, Quebec, Canada.
  • Atallah A; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Swaby A; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Dankner M; Rosalind and Morris Goodman Cancer Institute, McGill University, Montréal, Quebec, Canada.
  • Crump T; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Walsh LA; Rosalind and Morris Goodman Cancer Institute, McGill University, Montréal, Quebec, Canada.
  • Fiset PO; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Sepesi B; Rosalind and Morris Goodman Cancer Institute, McGill University, Montréal, Quebec, Canada.
  • Forde PM; Faculty of Medicine and Health Sciences, McGill University, Montréal, Quebec, Canada.
  • Cascone T; Department of Surgery, McGill University, Montréal, Quebec, Canada.
  • Provencio M; Rosalind and Morris Goodman Cancer Institute, McGill University, Montréal, Quebec, Canada.
  • Spicer JD; Department of Human Genetics, McGill University, Montréal, Quebec, Canada.
JAMA Oncol ; 10(5): 621-633, 2024 May 01.
Article em En | MEDLINE | ID: mdl-38512301
ABSTRACT
Importance To date, no meta-analyses have comprehensively assessed the association of neoadjuvant chemoimmunotherapy with clinical outcomes in non-small cell lung cancer (NSCLC) in randomized and nonrandomized settings. In addition, there exists controversy concerning the efficacy of neoadjuvant chemoimmunotherapy for patients with NSCLC with programmed cell death 1 ligand 1 (PD-L1) levels less than 1%.

Objective:

To compare neoadjuvant chemoimmunotherapy with chemotherapy by adverse events and surgical, pathological, and efficacy outcomes using recently published randomized clinical trials and nonrandomized trials. Data Sources MEDLINE and Embase were systematically searched from January 1, 2013, to October 25, 2023, for all clinical trials of neoadjuvant chemoimmunotherapy and chemotherapy that included at least 10 patients. Study Selection Observational studies and trials reporting the use of neoadjuvant radiotherapy, including chemoradiotherapy, molecular targeted therapy, or immunotherapy monotherapy, were excluded. Main Outcomes and

Measures:

Surgical, pathological, and efficacy end points and adverse events were pooled using a random-effects meta-analysis.

Results:

Among 43 eligible trials comprising 5431 patients (4020 males [74.0%]; median age range, 55-70 years), there were 8 randomized clinical trials with 3387 patients. For randomized clinical trials, pooled overall survival (hazard ratio, 0.65; 95% CI, 0.54-0.79; I2 = 0%), event-free survival (hazard ratio, 0.59; 95% CI, 0.52-0.67; I2 = 14.9%), major pathological response (risk ratio, 3.42; 95% CI, 2.83-4.15; I2 = 31.2%), and complete pathological response (risk ratio, 5.52; 95% CI, 4.25-7.15; I2 = 27.4%) favored neoadjuvant chemoimmunotherapy over neoadjuvant chemotherapy. For patients with baseline tumor PD-L1 levels less than 1%, there was a significant benefit in event-free survival for neoadjuvant chemoimmunotherapy compared with chemotherapy (hazard ratio, 0.74; 95% CI, 0.62-0.89; I2 = 0%). Conclusion and Relevance This study found that neoadjuvant chemoimmunotherapy was superior to neoadjuvant chemotherapy across surgical, pathological, and efficacy outcomes. These findings suggest that patients with resectable NSCLC with tumor PD-L1 levels less than 1% may have an event-free survival benefit with neoadjuvant chemoimmunotherapy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Terapia Neoadjuvante / Imunoterapia / Neoplasias Pulmonares Limite: Aged / Humans / Middle aged Idioma: En Revista: JAMA Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Terapia Neoadjuvante / Imunoterapia / Neoplasias Pulmonares Limite: Aged / Humans / Middle aged Idioma: En Revista: JAMA Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá