Outcome of chemoradiotherapy using intensity-modulated radiation therapy for cervical esophageal cancer: a single institute experience

Background The role of intensity-modulated radiation therapy in the treatment of cervical esophageal cancer remains unclear. The outcome of concurrent chemoradiotherapy for cervical esophageal squamous cell carcinoma using intensity-modulated radiation therapy was retrospectively evaluated. Methods...

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Veröffentlicht in:Esophagus : official journal of the Japan Esophageal Society 2021-07, Vol.18 (3), p.638-644
Hauptverfasser: Inada, Masahiro, Nishimura, Yasumasa, Ishikawa, Kazuki, Uehara, Takuya, Wada, Yutaro, Oguma, Yasuo, Doi, Hiroshi, Nakamatsu, Kiyoshi
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Sprache:eng
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Zusammenfassung:Background The role of intensity-modulated radiation therapy in the treatment of cervical esophageal cancer remains unclear. The outcome of concurrent chemoradiotherapy for cervical esophageal squamous cell carcinoma using intensity-modulated radiation therapy was retrospectively evaluated. Methods Between 2004 and 2017, 36 patients with cervical esophageal cancer treated with intensity-modulated radiation therapy were included. Among these patients, one had stage II disease, three stage III, 19 stage IVA, and 13 stage IVB. All patients received radiotherapy at a dose of 60 Gy and concurrent platinum-based doublet chemotherapy. Results The median follow-up period for surviving patients was 36 months. Three-year locoregional control, progression-free survival, and overall survival rates were 54, 40, and 46%, respectively. Disease progression was noted in 20 out of 36 patients (56%). Grade 3 late toxicities were observed in four patients (three esophageal stenoses and one carotid artery stenosis). There were no grade 4–5 toxicities. Univariate analysis identified the duration of radiotherapy as a prognostic factor for overall survival. Conclusions Chemoradiotherapy using intensity-modulated radiation therapy for locally advanced cervical esophageal carcinoma achieved satisfactory locoregional control and survival with acceptable toxicities.
ISSN:1612-9059
1612-9067
DOI:10.1007/s10388-020-00812-y