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Long-term outcomes following stereotactic body radiotherapy boost for oropharyngeal squamous cell carcinoma.

Authors :
Baker, Sarah
Verduijn, Gerda M.
Petit, Steven
Sewnaik, Aniel
Mast, Hetty
Koljenović, Senada
Nuyttens, Joost J.
Heemsbergen, Wilma D.
Source :
Acta Oncologica; Jun2019, Vol. 58 Issue 6, p926-933, 8p, 3 Charts, 3 Graphs
Publication Year :
2019

Abstract

Background/purpose: To determine the efficacy and toxicity profile of a stereotactic body radiotherapy (SBRT) boost as a first line treatment in patients with oropharyngeal squamous cell carcinoma (OPSCC). Materials and methods: We performed a retrospective cohort study in 195 consecutive OPSCC patients with T1-small T3 disease, treated at Erasmus MC between 2009 and 2016 with a SBRT (3 × 5.5 Gy) boost after 46 Gy IMRT. Primary endpoints were disease-specific survival (DSS) and Grade ≥3 toxicity (Common Terminology Criteria). The Kaplan-Meier method and Cox regression model were applied to determine rates and risk factors. Results: The median follow-up was 4.3 years. Treatment compliance was high (100%). Rates of 5-year DSS and late grade ≥3 toxicity were 85% and 28%, respectively. Five-year overall survival was 67%. The most frequently observed toxicities were mucosal ulceration or soft tissue necrosis (n = 30, 5 year 18%), dysphagia or weight loss (n = 18, 5 year 12%) and osteoradionecrosis (n = 11, 5 year 9%). Current smoker status (hazard ratio [HR] = 2.9, p =.001) and Charlson Comorbidity Index ≥2 (HR = 1.9, p =.03) were was associated with increased toxicity risk. Tooth extraction prior to RT was associated with increased osteoradionecrosis risk (HR = 6.4, p =.006). Conclusion: We reported on outcomes in the largest patient series to date treated with a hypofractionated boost for OPSCC. Efficacy was good with survival rates comparable to conventionally fractionated (chemo)radiotherapy. Grade ≥3 toxicity profiles showed high rates of soft tissue necrosis and osteoradionecrosis. Strategies to mitigate severe toxicity risks are under investigation to improve the tolerability of the SBRT boost. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0284186X
Volume :
58
Issue :
6
Database :
Complementary Index
Journal :
Acta Oncologica
Publication Type :
Academic Journal
Accession number :
136689710
Full Text :
https://doi.org/10.1080/0284186X.2019.1581375