| Literature DB >> 35294576 |
Markus Hecht1, Jens von der Grün2, Sabine Semrau3, Sarina Müller4, Thomas Weissmann3, Udo S Gaipl3, Heinrich Iro4, Rainer Fietkau3, Antoniu-Oreste Gostian4.
Abstract
At this year's annual meetings of the American Society of Clinical Oncology (ASCO) and the European Society for Medical Oncology (ESMO), several studies on radiotherapy of locally advanced head and neck cancer were presented. For the indication of definitive radiochemotherapy, particularly the administration of immune checkpoint inhibitors concomitant to radiotherapy was investigated. In the phase III GORTEC-REACH trial, combined inhibition of epidermal growth factor receptor (EGFR) and programmed death-ligand (PD-L1) concomitant to radiotherapy of locally advanced head and neck cancer was inferior to platinum-based chemoradiotherapy. However, this therapeutic approach may be more efficient than radiotherapy with simultaneous EGFR inhibition alone. The concept of the phase II CheckRad-CD8 trial with induction chemoimmunotherapy followed by chemotherapy-free radioimmunotherapy after appropriate patient selection also proved to be highly efficient. In initial phase II trials, dose de-escalation of radiotherapy seems feasible for HPV-positive oropharyngeal cancer after appropriate patient selection both postoperatively (ECOG-ACRIN E3311 trial) and after induction therapy (Optima II trial). However, dose de-escalation should currently not be performed outside of clinical trials. In addition, first studies indicate a benefit of functional imaging (diffusion-weighted magnetic resonance imaging [MRI] or F‑fluoromisonidazole positron-emission tomography [FMISO-PET]) to establish personalized dose concepts in radiotherapy.Entities:
Keywords: Chemoradiotherapy; Head and neck squamous cell carcinoma; Human papillomavirus; Immunotherapy; Oropharyngeal cancer
Mesh:
Year: 2022 PMID: 35294576 DOI: 10.1007/s00106-022-01150-4
Source DB: PubMed Journal: HNO ISSN: 0017-6192 Impact factor: 1.284