The Emerging Role of Immunotherapy in Resectable Non-Small Cell Lung Cancer.
Journal
The Annals of thoracic surgery
ISSN: 1552-6259
Titre abrégé: Ann Thorac Surg
Pays: Netherlands
ID NLM: 15030100R
Informations de publication
Date de publication:
03 Feb 2024
03 Feb 2024
Historique:
received:
25
10
2023
revised:
09
01
2024
accepted:
22
01
2024
medline:
6
2
2024
pubmed:
6
2
2024
entrez:
5
2
2024
Statut:
aheadofprint
Résumé
Despite surgical resection, long-term survival of patients with resectable non-small cell lung cancer (NSCLC) remains poor. Adjuvant chemotherapy, the standard of care for locally advanced NSCLC, provides a marginal 5.4% benefit in survival. Immune checkpoint inhibitors (ICIs) have shown a significant survival benefit in some patients with advanced NSCLC and are being evaluated for perioperative use in resectable NSCLC. We conducted a literature search using the PubMed online database to identify clinical trials of immunotherapy in resectable NSCLC and studies analyzing biomarkers and immune priming strategies. Building upon previous phase I and II trials, CheckMate 816, KEYNOTE-671, IMpower010, and PEARLS/KEYNOTE-091 have shown efficacy of neoadjuvant nivolumab, perioperative pembrolizumab, adjuvant atezolizumab and adjuvant pembrolizumab, respectively, with improvement of event-free/disease-free survival of 24-42%, leading to FDA approval of these drugs in the treatment of resectable NSCLC. Phase III trials CheckMate 77T, AEGEAN, and Neotorch have also recently reported the use of immunotherapy both before and after surgery with pathologic complete response rates of 17%-25%, significantly better than chemotherapy alone. Perioperative ICI therapy has comparable perioperative morbidity to chemotherapy alone and does not impair surgical outcomes. Perioperative immunotherapy, in combination with chemotherapy, is safe and improves outcomes in patients with resectable NSCLC. Questions regarding patient selection, the need for adjuvant ICI therapy after neoadjuvant chemoimmunotherapy, and the duration of perioperative immunotherapy remain to be answered by future trials.
Sections du résumé
BACKGROUND
BACKGROUND
Despite surgical resection, long-term survival of patients with resectable non-small cell lung cancer (NSCLC) remains poor. Adjuvant chemotherapy, the standard of care for locally advanced NSCLC, provides a marginal 5.4% benefit in survival. Immune checkpoint inhibitors (ICIs) have shown a significant survival benefit in some patients with advanced NSCLC and are being evaluated for perioperative use in resectable NSCLC.
METHODS
METHODS
We conducted a literature search using the PubMed online database to identify clinical trials of immunotherapy in resectable NSCLC and studies analyzing biomarkers and immune priming strategies.
RESULTS
RESULTS
Building upon previous phase I and II trials, CheckMate 816, KEYNOTE-671, IMpower010, and PEARLS/KEYNOTE-091 have shown efficacy of neoadjuvant nivolumab, perioperative pembrolizumab, adjuvant atezolizumab and adjuvant pembrolizumab, respectively, with improvement of event-free/disease-free survival of 24-42%, leading to FDA approval of these drugs in the treatment of resectable NSCLC. Phase III trials CheckMate 77T, AEGEAN, and Neotorch have also recently reported the use of immunotherapy both before and after surgery with pathologic complete response rates of 17%-25%, significantly better than chemotherapy alone. Perioperative ICI therapy has comparable perioperative morbidity to chemotherapy alone and does not impair surgical outcomes.
CONCLUSIONS
CONCLUSIONS
Perioperative immunotherapy, in combination with chemotherapy, is safe and improves outcomes in patients with resectable NSCLC. Questions regarding patient selection, the need for adjuvant ICI therapy after neoadjuvant chemoimmunotherapy, and the duration of perioperative immunotherapy remain to be answered by future trials.
Identifiants
pubmed: 38316378
pii: S0003-4975(24)00080-8
doi: 10.1016/j.athoracsur.2024.01.024
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024. Published by Elsevier Inc.