Plasma Proteomic Analysis in Non-Small Cell Lung Cancer Patients Treated with PD-1/PD-L1 Blockade.

PD-L1 biomarkers immune checkpoint inhibitors liquid biopsy lung cancer

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
22 Jun 2021
Historique:
received: 14 05 2021
revised: 17 06 2021
accepted: 18 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

Checkpoint inhibitors have been approved for the treatment of non-small cell lung cancer (NSCLC). However, only a minority of patients demonstrate a durable clinical response. PD-L1 scoring is currently the only biomarker measure routinely used to select patients for immunotherapy, but its predictive accuracy is modest. The aim of our study was to evaluate a proteomic assay for the analysis of patient plasma in the context of immunotherapy. Pretreatment plasma samples from 43 NSCLC patients who received anti-PD-(L)1 therapy were analyzed using a proximity extension assay (PEA) to quantify 92 different immune oncology-related proteins. The plasma protein levels were associated with clinical and histopathological parameters, as well as therapy response and survival. Unsupervised hierarchical cluster analysis revealed two patient groups with distinct protein profiles associated with high and low immune protein levels, designated as "hot" and "cold". Further supervised cluster analysis based on T-cell activation markers showed that higher levels of T-cell activation markers were associated with longer progression-free survival (PFS) (

Identifiants

pubmed: 34206510
pii: cancers13133116
doi: 10.3390/cancers13133116
pmc: PMC8268315
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Sjöberg Foundation
ID : #1
Organisme : Cancerfonden
ID : CAN2015/709 and CAN2018/816

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Auteurs

Mohamed Eltahir (M)

Department of Immunology, Genetics and Pathology, Uppsala University, 751 85 Uppsala, Sweden.
Department of Pharmaceutical Biosciences, Science for Life Laboratory, Uppsala University, 751 24 Uppsala, Sweden.

Johan Isaksson (J)

Department of Immunology, Genetics and Pathology, Uppsala University, 751 85 Uppsala, Sweden.
Centre for Research and Development, Uppsala University, Region Gävleborg, 801 88 Uppsala, Sweden.

Johanna Sofia Margareta Mattsson (JSM)

Department of Immunology, Genetics and Pathology, Uppsala University, 751 85 Uppsala, Sweden.

Klas Kärre (K)

Department of Microbiology, Cell and Tumor Biology, Karolinska Institute, 171 77 Stockholm, Sweden.

Johan Botling (J)

Department of Immunology, Genetics and Pathology, Uppsala University, 751 85 Uppsala, Sweden.

Martin Lord (M)

Department of Pharmaceutical Biosciences, Science for Life Laboratory, Uppsala University, 751 24 Uppsala, Sweden.

Sara M Mangsbo (SM)

Department of Pharmaceutical Biosciences, Science for Life Laboratory, Uppsala University, 751 24 Uppsala, Sweden.

Patrick Micke (P)

Department of Immunology, Genetics and Pathology, Uppsala University, 751 85 Uppsala, Sweden.

Classifications MeSH