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
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.

Auteurs

Elizabeth G Dunne (EG)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.

Cameron N Fick (CN)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.

James M Isbell (JM)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.

Jamie E Chaft (JE)

Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Nasser Altorki (N)

Department of Cardiothoracic Surgery, Weill Cornell Medicine, New York, NY.

Bernard J Park (BJ)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.

Jonathan Spicer (J)

Department of Thoracic Surgery, McGill University Health Centre, Montreal, Quebec, Canada.

Patrick M Forde (PM)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD.

Daniel Gomez (D)

Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.

Puneeth Iyengar (P)

Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.

David H Harpole (DH)

Division of Cardiovascular and Thoracic Surgery, Duke University Medical Center, Durham, NC.

Thomas E Stinchcombe (TE)

Division of Medical Oncology, Duke Cancer Institute, Duke University Medical Center, Durham, NC.

Moishe Liberman (M)

Division of Thoracic Surgery, University of Montreal, Montreal, Quebec, Canada.

Matthew J Bott (MJ)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.

Prasad S Adusumilli (PS)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.

James Huang (J)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.

Gaetano Rocco (G)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.

David R Jones (DR)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY. Electronic address: jonesd2@mskcc.org.

Classifications MeSH