Immunotherapy-chemotherapy combinations for non-small cell lung cancer: current trends and future perspectives.

NSCLC anti-CTLA4 anti-PD-L1 anti-PD1 immune-checkpoint inhibitors immunotherapy immunotherapy-chemotherapy combination lung cancer

Journal

Expert opinion on biological therapy
ISSN: 1744-7682
Titre abrégé: Expert Opin Biol Ther
Pays: England
ID NLM: 101125414

Informations de publication

Date de publication:
10 2022
Historique:
pubmed: 23 8 2022
medline: 22 10 2022
entrez: 22 8 2022
Statut: ppublish

Résumé

In recent years, immunotherapy has become a pillar in the treatment of advanced, non-oncogene-addicted non-small cell lung cancer (NSCLC). Programmed death ligand 1 (PD-L1) expression is currently the only factor used to predict response to immunotherapy in clinical practice. Specifically, single-agent pembrolizumab as first-line therapy is approved for tumors with high expression of PD-L1 (≥50%) while immunotherapy and chemotherapy are approved for any PD-L1. However, combinations of immune-checkpoint inhibitors (ICIs) and other agents may confer higher benefit than immunotherapy alone in some circumstances. We reviewed the available data regarding the combined use of ICIs and chemotherapy in patients with advanced, treatment-naïve NSCLC. In light of the benefit demonstrated in advanced disease, these combinations have been subsequently tested in other settings. We collected the most relevant findings regarding efficacy and safety of chemo-immunotherapy combinations in early and locally advanced NSCLC. Immune-chemotherapy combinations demonstrated benefit in the advanced setting, and this strategy in now being applied in the early and local advanced settings. A description of clinical and biological predictors of response is required in order to identify patients who may benefit the most from combination therapy.

Identifiants

pubmed: 35994596
doi: 10.1080/14712598.2022.2116273
doi:

Substances chimiques

B7-H1 Antigen 0
Immune Checkpoint Inhibitors 0
Programmed Cell Death 1 Receptor 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1259-1273

Auteurs

Eugenia Cella (E)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Lodovica Zullo (L)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Silvia Marconi (S)

IRCCS Ospedale Policlinico San Martino, UO Tumori Polmonari, Genoa, Italy.

Giovanni Rossi (G)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Simona Coco (S)

IRCCS Ospedale Policlinico San Martino, UO Tumori Polmonari, Genoa, Italy.

Chiara Dellepiane (C)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Angela Alama (A)

IRCCS Ospedale Policlinico San Martino, UO Tumori Polmonari, Genoa, Italy.

Leslie Rozeboom (L)

Department of Pathology, Anschutz Medical Campus, Aurora, Colorado, USA.

Elisa Bennicelli (E)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Francesca Parisi (F)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Gianluca Sacco (G)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Giulia Barletta (G)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Linda Zinoli (L)

IRCCS Ospedale Policlinico San Martino, UO Clinica di Oncologia Medica, Genoa, Italy.

Marco Tagliamento (M)

Dipartimento di Medicina Interna (DiMI), Università degli Studi di Genova, Genoa, Italy.

Paolo Pronzato (P)

IRCCS Ospedale Policlinico San Martino, UO Oncologia Medica 2, Genoa, Italy.

Carlo Genova (C)

IRCCS Ospedale Policlinico San Martino, UO Clinica di Oncologia Medica, Genoa, Italy.
Dipartimento di Medicina Interna (DiMI), Università degli Studi di Genova, Genoa, Italy.

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Classifications MeSH