Advancing neoadjuvant therapies in resectable non-small cell lung cancer: implications for novel treatment strategies and biomarker discovery.
NSCLC
adjuvant
lung cancer
neoadjuvant
perioperative
Journal
Pathology oncology research : POR
ISSN: 1532-2807
Titre abrégé: Pathol Oncol Res
Pays: Switzerland
ID NLM: 9706087
Informations de publication
Date de publication:
2024
2024
Historique:
received:
02
05
2024
accepted:
04
06
2024
medline:
3
7
2024
pubmed:
3
7
2024
entrez:
3
7
2024
Statut:
epublish
Résumé
The delivery of neoadjuvant and perioperative therapies for non-small cell lung cancer has been radically altered by significant advances and by the incorporation of targeted therapies as well as immune checkpoint inhibitors alone or alongside conventional chemotherapy. This evolution has been particularly notable in the incorporation of immunotherapy and targeted therapy into the treatment of resectable NSCLC, where recent FDA approvals of drugs such as nivolumab and pembrolizumab, in combination with platinum doublet chemotherapy, have led to considerable improvements in pathological complete response rates and the potential for enhanced long-term survival outcomes. This review emphasizes the growing importance of biomarkers in optimizing treatment selection and explores the impact of emerging studies that challenge existing treatment paradigms and investigate novel therapeutic combinations poised to redefine standard of care practices. Furthermore, the discussion extends to the unmet needs within perioperative treatment assessment and prognostication, highlighting the prospective value of biomarkers in evaluating treatment responses and prognosis.
Identifiants
pubmed: 38957347
doi: 10.3389/pore.2024.1611817
pii: 1611817
pmc: PMC11217184
doi:
Substances chimiques
Biomarkers, Tumor
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1611817Informations de copyright
Copyright © 2024 Jeon, Gor, D’Aiello, Stiles, Illei and Halmos.
Déclaration de conflit d'intérêts
BH—Receives clinical research funding from Boehringer Ingelheim, Astra Zeneca, Merck, BMS, Advaxis, Amgen, AbbVie, Daiichi, Pfizer, GSK, Beigene, Janssen, Black Diamond Therapeutics, Forward Pharma, Numab, Arrivent. Receives Honoraria from Astra Zeneca, Boehringer Ingelheim, Apollomics, Janssen, Takeda, Merck, BMS, Genentech, Pfizer, Eli-Lilly, Arcus, Merus, Daiichi, Precede. BS—Provides consulting and serves as advisory boards for Medtronic, AstraZeneca, Roche-Genentech, Pfizer, Arcus Biosciences, Bristol Myers Squib, Merck, Regeneron, Galvanize Therapeutics. Receives research funding from BMS Foundation and his wife owns salary/stock for SIGA Technologies. PI—Serves as advisory board for Agilent, AstraZeneca, Sanofi, AbbVie, Genentech, Merus, and speaks for Eli Lilly. Receives research funding from Bristol Myers-Squib. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.