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Tumor DNA-methylome derived epigenetic fingerprint identifies HPV-negative head and neck patients at risk for locoregional recurrence after postoperative radiochemotherapy

Authors :
Tawk, B.
Wirkner, U.
Schwager, C.
Rein, K.
Zaoui, K.
Federspil, P. A.
Adeberg, S.
Linge, A.
Ganswindt, U.
Hess, J.
Unger, K.
Tinhofer, I.
Budach, V.
Lohaus, F.
Krause, M.
Guberina, M.
Stuschke, M.
Balermpas, P.
Rödel, C.
Grosu, A. L.
Schäfer, H.
Zips, D.
Combs, S. E.
Pigorsch, S.
Zitzelsberger, H.
Baumeister, P.
Kirchner, T.
Bewerunge-Hudler, M.
Weichert, W.
Herpel, E.
Belka, C.
Baumann, M.
Debus, J.
Abdollahi, A.
DKTK-ROG
Source :
International Journal of Cancer 150(2022), 603-616
Publication Year :
2022

Abstract

Biomarkers with relevance for loco-regional therapy are needed in human papillomavirus negative aka HPV(-) head and neck squamous cell carcinoma (HNSCC). Based on the premise that DNA methylation pattern is highly conserved, we sought to develop a reliable and robust methylome-based classifier identifying HPV(-) HNSCC patients at risk for loco-regional recurrence (LR) and all-event progression after postoperative radiochemotherapy (PORT-C). The training cohort consisted of HPV-DNA negative HNSCC patients (n = 128) homogeneously treated with PORT-C in frame of the German Cancer Consortium-Radiation Oncology Group (DKTK-ROG) multicenter biomarker trial. DNA Methylation analysis was performed using Illumina 450 K and 850 K-EPIC microarray technology. The performance of the classifier was integrated with a series of biomarkers studied in the training set namely hypoxia-, 5-microRNA (5-miR), stem-cell gene-expression signatures and immunohistochemistry (IHC)-based immunological characterization of tumors (CD3/CD8/PD-L1/PD1). Validation occurred in an independent cohort of HPV(-) HNSCC patients, pooled from two German centers (n = 125). We identified a 38-methylation probe-based HPV(-) Independent Classifier of disease Recurrence (HICR) with high prognostic value for LR, distant metastasis and overall survival (P < 10-9 ). HICR remained significant after multivariate analysis adjusting for anatomical site, lymph node extracapsular extension (ECE) and size (T-stage). HICR high-risk tumors were enriched for younger patients with hypoxic tumors (15-gene signature) and elevated 5-miR score. After adjustment for hypoxia and 5-miR covariates, HICR maintained predicting all endpoints. HICR provides a novel mean for assessing the risk of LR in HPV(-) HNSCC patients treated with PORT-C and opens a new opportunity for biomarker-assisted stratification and therapy adaptation in these patients.

Details

Language :
English
Database :
OpenAIRE
Journal :
International Journal of Cancer 150(2022), 603-616
Accession number :
edsair.od......4577..2816f538ca3c35cd8288da68134e7b3b