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Ovarian cancer-derived copy number alterations signatures are prognostic in chemoradiotherapy-treated head and neck squamous cell carcinoma
Authors:Paul B.M. Essers  Martijn van der Heijden  David Vossen  Reinout H. de Roest  C. René Leemans  Ruud H. Brakenhoff  Michiel W.M. van den Brekel  Harry Bartelink  Marcel Verheij  Conchita Vens
Affiliation:1. Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands;2. 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;3. Amsterdam UMC, Vrije Universiteit Amsterdam, Otolaryngology/Head and Neck Surgery, Cancer Center Amsterdam, The Netherlands;4. Department of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, Amsterdam, The Netherlands;5. Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands;6. Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands

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

Abstract: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.
Keywords:copy number alterations  head and neck squamous cell carcinoma  chemoradiotherapy  prognosis  cisplatin  HNSCC
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