A Phase I/II Clinical Trial of Preoperative Short-Course Carbon-Ion Radiotherapy for Patients With Squamous Cell Carcinoma of the Esophagus

被引:33
作者
Akutsu, Yasunori [1 ,2 ]
Yasuda, Shigeo [1 ,3 ]
Nagata, Matsuo [1 ,4 ]
Izumi, Yosuke [1 ,5 ]
Okazumi, Shinichi [1 ,6 ]
Shimada, Hideaki [1 ,7 ]
Nakatani, Yukio [1 ,8 ]
Tsujii, Hirohiko [1 ,3 ]
Kamada, Tadashi [1 ,3 ]
Yamada, Shigeru [1 ,3 ]
Matsubara, Hisahiro [1 ,2 ]
机构
[1] Investigators Working Grp Gastrointestinal Tumors, Chiba, Japan
[2] Chiba Univ, Grad Sch Med, Dept Frontier Surg, Chiba, Japan
[3] Natl Inst Radiol Sci, Res Ctr Hosp Charged Particle Therapy, Chiba 260, Japan
[4] Chiba Canc Ctr, Dept Surg, Chiba 2608717, Japan
[5] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Dept Surg, Tokyo, Japan
[6] Toho Univ, Sakura Med Ctr, Dept Surg, Chiba 2748510, Japan
[7] Toho Univ, Sch Med, Omori Med Ctr, Dept Surg, Tokyo, Japan
[8] Chiba Univ, Grad Sch Med, Dept Diagnost Pathol, Chiba, Japan
关键词
esophageal cancer; carbon-ion radiotherapy; heavy-ion radiotherapy; neoadjuvant therapy; surgery; squamous cell carcinoma; LYMPH-NODE METASTASES; RADIATION-THERAPY; NEOADJUVANT CHEMORADIOTHERAPY; PROGNOSTIC-SIGNIFICANCE; IRRADIATION SYSTEM; CANCER; CHEMORADIATION; SURGERY; METAANALYSIS; NUMBER;
D O I
10.1002/jso.22127
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Carbon-ion radiotherapy (CIR) has been under development. We report the results of a phase I/II clinical trial of preoperative CIR for esophageal squamous cell carcinoma (ESCC). Methods: Thirty-one thoracic ESCC patients were enrolled. They were first treated with CIR. The radiation dose was escalated from the initial dose of 28.8 GyE up to 36.8. Four to 8 weeks after CIR followed by clinical evaluation of the therapy, surgery was performed. Thereafter, a pathological evaluation was made. Results: Acute toxicity was not seen except in one case (3.2%), and there were no late toxicities. Throughout the study period, there were no cases of withdrawal due to the effects of preoperative CIR. Twelve out of 31 (38.7%) patients achieved a clinical complete response (CR) and 13 patients (41.9%) achieved a partial response. Twelve out of 31 patients (38.7%) achieved a pathological CR. The overall 1-, 3-, and 5-year survival rates in the stage I cases were 91%, 81%, and 61%, and was 100%, 85%, and 77% for the stage II, and 71%, 43%, and 29% for the stage III cases, respectively. Conclusions: CIR showed strong local tumor control and is highly effective as a neoadjuvant therapy without severe adverse events. J. Surg. Oncol. 2012; 105:750-755. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:750 / 755
页数:6
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