Ovarian cancer-derived copy number alterations signatures are prognostic in chemoradiotherapy-treated head and neck squamous cell carcinoma.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
15 09 2020
Historique:
received: 29 10 2019
revised: 17 01 2020
accepted: 11 02 2020
pubmed: 14 3 2020
medline: 15 4 2021
entrez: 14 3 2020
Statut: ppublish

Résumé

DNA copy number alterations (CNAs) are frequent in cancer, and recently developed CNA signatures revealed their value in molecular tumor stratification for patient prognosis and platinum resistance prediction in ovarian cancer. Head and neck squamous cell carcinoma (HNSCC) is also characterized by high CNAs. In this study, we determined CNA in 173 human papilloma virus-negative HNSCC from a Dutch multicenter cohort by low-coverage whole genome sequencing and tested the prognostic value of seven cancer-derived CNA signatures for these cisplatin- and radiotherapy-treated patients. We find that a high CNA signature 1 (s1) score is associated with low values for all other signatures and better patient outcomes in the Dutch cohorts and The Cancer Genome Atlas HNSCC data set. High s5 and s7 scores are associated with increased distant metastasis rates and high s6 scores with poor overall survival. High cumulative cisplatin doses result in improved outcomes in chemoradiotherapy-treated HNSCC patients. Here we find that tumors high in s1 or low in s6 are most responsive to a change in cisplatin dose. High s5 values, however, significantly increase the risk for metastasis in patients with low cumulative cisplatin doses. Together this suggests that the processes causing these CNA signatures affect cisplatin response in HNSCC. In conclusion, CNA signatures derived from a different cancer type were prognostic and associated with cisplatin response in HNSCC, suggesting they represent underlying molecular processes that define patient outcome.

Identifiants

pubmed: 32167160
doi: 10.1002/ijc.32962
pmc: PMC7496441
doi:

Substances chimiques

Biomarkers, Tumor 0
Cisplatin Q20Q21Q62J

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1732-1739

Informations de copyright

© 2020 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.

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Auteurs

Paul B M Essers (PBM)

Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Martijn van der Heijden (M)

Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

David Vossen (D)

Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Reinout H de Roest (RH)

Amsterdam UMC, Vrije Universiteit Amsterdam, Otolaryngology/Head and Neck Surgery, Cancer Center Amsterdam, The Netherlands.

C René Leemans (CR)

Amsterdam UMC, Vrije Universiteit Amsterdam, Otolaryngology/Head and Neck Surgery, Cancer Center Amsterdam, The Netherlands.

Ruud H Brakenhoff (RH)

Amsterdam UMC, Vrije Universiteit Amsterdam, Otolaryngology/Head and Neck Surgery, Cancer Center Amsterdam, The Netherlands.

Michiel W M van den Brekel (MWM)

Department of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Harry Bartelink (H)

Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Marcel Verheij (M)

Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Conchita Vens (C)

Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

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Classifications MeSH