Biomarkers Associated with Immune-Related Adverse Events under Checkpoint Inhibitors in Metastatic Melanoma.

genetic alterations immune-related adverse events immunotherapies melanoma

Journal

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

Informations de publication

Date de publication:
08 Jan 2022
Historique:
received: 17 12 2021
accepted: 04 01 2022
entrez: 21 1 2022
pubmed: 22 1 2022
medline: 22 1 2022
Statut: epublish

Résumé

Immune checkpoint inhibitors (ICI) have revolutionized the therapeutic landscape of metastatic melanoma. However, ICI are often associated with immune-related adverse events (IRAE) such as colitis, hepatitis, pancreatitis, hypophysitis, pneumonitis, thyroiditis, exanthema, nephritis, myositis, encephalitis, or myocarditis. Biomarkers associated with the occurrence of IRAE would be desirable. In the literature, there is only little data available and furthermore mostly speculative, especially in view of genetic alterations. Our major aim was to check for possible associations between NGS-based genetic alterations and IRAE. We therefore analyzed 95 melanoma patients with ICI and evaluated their NGS results. We checked the data in view of potential associations between copy number variations (CNVs), small variations (VARs), human leucocyte antigen (HLA), sex, blood count parameters, pre-existing autoimmune diseases and the occurrence of IRAE. We conducted a literature research on genetic alterations hypothesized to be associated with the occurrence of IRAE. In total, we identified 39 genes that have been discussed as hypothetical biomarkers. We compared the list of these 39 genes with the tumor panel that our patients had received and focused our study on those 16 genes that were also included in the tumor panel used for NGS. Therefore, we focused our analyses on the following genes:

Identifiants

pubmed: 35053465
pii: cancers14020302
doi: 10.3390/cancers14020302
pmc: PMC8773840
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Marcus Wölffer (M)

Department of Dermatology, University Hospital Tuebingen, 72076 Tuebingen, Germany.

Florian Battke (F)

Center for Genomics and Transcriptomics (CeGaT) GmbH, 72076 Tuebingen, Germany.

Martin Schulze (M)

Practice for Human Genetics, 72076 Tuebingen, Germany.

Magdalena Feldhahn (M)

Center for Genomics and Transcriptomics (CeGaT) GmbH, 72076 Tuebingen, Germany.

Lukas Flatz (L)

Department of Dermatology, University Hospital Tuebingen, 72076 Tuebingen, Germany.

Peter Martus (P)

Institute for Clinical Epidemiology and Applied Biostatistics (IKEaB), 72076 Tuebingen, Germany.

Andrea Forschner (A)

Department of Dermatology, University Hospital Tuebingen, 72076 Tuebingen, Germany.

Classifications MeSH