@article{1223cd69ad9e4fa8834312194ef8a169,
title = "Current status of immune checkpoint inhibition in early-stage NSCLC",
abstract = "Immune checkpoint inhibition (ICI) immunotherapy has revolutionized the approach to metastatic non-small-cell lung cancer (NSCLC). In particular, antibodies blocking the inhibitory immune checkpoints programmed death 1 (PD-1) and its ligand (PD-L1) are associated with higher response rates, improved overall survival and better tolerability as compared with conventional cytotoxic chemotherapy. Recently, ICI has moved from the second-line to the first-line setting for many patients with non-oncogene-addicted NSCLC, either alone or in combination with chemotherapy. The next logical step is to examine this therapy in patients with non-metastatic NSCLC to improve long-term overall survival and cure rates. For patients with unresectable stage III NSCLC, ICI with durvalumab after concurrent chemoradiotherapy has brought a major improvement in 2-year progression-free and overall survival, which holds promise for an improved cure rate. As the relapse pattern in patients with completely resected early-stage NSCLC is predominantly systemic, high expectations rest on the integration of ICI therapy in their treatment approach. A large number of studies with adjuvant or neo-adjuvant ICI are ongoing and will be discussed here. The advent of stereotactic ablative radiotherapy has brought a valid alternative treatment of patients unfit for or not willing to undergo surgery. Data on combining systemic therapy and stereotactic ablative radiotherapy are virtually non-existent, but there is a strong biological rationale to combine radiotherapy and ICI therapy. Early findings in small feasibility studies are promising and now need to be explored in well-designed phase III trials.",
keywords = "immunotherapy, non-small-cell lung cancer, early stage, clinical trials, CELL-LUNG-CANCER, STEREOTACTIC ABLATIVE RADIOTHERAPY, TUMOR-REGRESSION, PHASE-II, RADIATION, IMMUNOTHERAPY, CHEMOTHERAPY, BLOCKADE, IRRADIATION, IPILIMUMAB",
author = "J. Vansteenkiste and E. Wauters and B. Reymen and Ackermann, {C. J.} and S. Peters and {De Ruysscher}, D.",
note = "Funding Information: University Hospitals KU Leuven: MSDAstraZenecaBoehringer-IngelheimCancer Belgium2017-2022Christie NHS Foundation TrustSwiss Cancer LeagueSwiss Group for Clinical Cancer ResearchSAKKFoundation Medicine Funding Information: JV received research funding at University Hospitals KU Leuven: MSD; advisory functions: AstraZeneca, Boehringer-Ingelheim, MSD, Novartis, Roche; lectures fees from AstraZeneca, BMS, Boehringer-Ingelheim, MSD, Roche. EW received research funding: mandate for clinical and translational oncology research of the Foundation against Cancer Belgium (2017-2022); received lectures fees from AstraZeneca, Boehringer-Ingelheim. CJA received research funding at Christie NHS Foundation Trust, Manchester, UK: Swiss Cancer League, Swiss Group for Clinical Cancer Research (SAKK). SP received research support/receipt of grants: (Sub)investigator in trials (institutional financial support for clinical trials) sponsored by Amgen, AstraZeneca, Boehringer-Ingelheim, BMS, Clovis, Roche, Illumina, MSD, Merck Serono, Novartis, and Pfizer; advisory functions: Abbvie, Amgen, AstraZeneca, Bayer, Biocartis, Boehringer-Ingelheim, BMS, Clovis, Daiichi Sankyo, Debiopharm, Eli Lilly, Roche, Foundation Medicine, Illumina, Janssen, MSD, Merck Serono, Merrimack, Novartis, Pharma Mar, Pfizer, Regeneron, Sanofi, Seattle Genetics and Takeda; lectures fees fromAstraZeneca, Boehringer-Ingelheim, BMS, Eli Lilly, Roche, MSD, Novartis, Pfizer, Takeda. DDR received research funding from Astra Zeneca, BMS; advisory functions: Astra Zeneca, BMS, Celgene, Roche/Genentech, Merck/Pfizer; lectures fees from Astra Zeneca, Pfizer. All remaining authors have declared no conflicts of interest. Publisher Copyright: {\textcopyright} 2019 The Author(s). Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved.",
year = "2019",
month = aug,
doi = "10.1093/annonc/mdz175",
language = "English",
volume = "30",
pages = "1244--1253",
journal = "Annals of Oncology",
issn = "0923-7534",
publisher = "Elsevier Ltd",
number = "8",
}