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


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

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.; Hess, J.; Herpel, E.; Belka, C.; Baumann, M.; Debus, J.; Abdollahi, A.; DKTK-ROG

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.

Keywords: DNA methylation; disease recurrence; head and neck cancers; radiotherapy; stratification

Permalink: https://www.hzdr.de/publications/Publ-33978