| Literature DB >> 33372202 |
Koichi Yasuda1, Hideki Minatogawa1,2, Yasuhiro Dekura1,3, Seishin Takao4, Masaya Tamura4, Nayuta Tsushima5, Takayoshi Suzuki5, Satoshi Kano5, Takatsugu Mizumachi5, Takashi Mori6, Kentaro Nishioka3, Motoyasu Shido1, Norio Katoh2, Hiroshi Taguchi1, Noriyuki Fujima7, Rikiya Onimaru2, Isao Yokota8, Keiji Kobashi4,3, Shinichi Shimizu3, Akihiro Homma5, Hiroki Shirato2, Hidefumi Aoyama2.
Abstract
Pharyngeal cancer patients treated with intensity-modulated proton therapy (IMPT) using a model-based approach were retrospectively reviewed, and acute toxicities were analyzed. From June 2016 to March 2019, 15 pharyngeal (7 naso-, 5 oro- and 3 hypo-pharyngeal) cancer patients received IMPT with robust optimization. Simulation plans for IMPT and intensity-modulated X-ray therapy (IMXT) were generated before treatment. We also reviewed 127 pharyngeal cancer patients with IMXT in the same treatment period. In the simulation planning comparison, all of the normal-tissue complication probability values for dysphagia, dysgeusia, tube-feeding dependence and xerostomia were lower for IMPT than for IMXT in the 15 patients. After completing IMPT, 13 patients completed the evaluation, and 12 of these patients had a complete response. The proportions of patients who experienced grade 2 or worse acute toxicities in the IMPT and IMXT cohorts were 21.4 and 56.5% for dysphagia (P < 0.05), 46.7 and 76.3% for dysgeusia (P < 0.05), 73.3 and 62.8% for xerostomia (P = 0.43), 73.3 and 90.6% for mucositis (P = 0.08) and 66.7 and 76.4% for dermatitis (P = 0.42), respectively. Multivariate analysis revealed that IMPT was independently associated with a lower rate of grade 2 or worse dysphagia and dysgeusia. After propensity score matching, 12 pairs of IMPT and IMXT patients were selected. Dysphagia was also statistically lower in IMPT than in IMXT (P < 0.05). IMPT using a model-based approach may have clinical benefits for acute dysphagia.Entities:
Keywords: IMPT; pharyngeal cancer; robust optimization
Year: 2021 PMID: 33372202 PMCID: PMC7948838 DOI: 10.1093/jrr/rraa130
Source DB: PubMed Journal: J Radiat Res ISSN: 0449-3060 Impact factor: 2.724