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局部复发性直肠癌的碳离子放疗:日本碳离子放射肿瘤学研究组(J-CROS)研究 1404 直肠。

Carbon-ion radiotherapy for locally recurrent rectal cancer: Japan Carbon-ion Radiation Oncology Study Group (J-CROS) Study 1404 Rectum.

机构信息

Ion Beam Therapy Center, SAGA HIMAT Foundation, Tosu, Japan.

National Institutional of Radiological Sciences Hospital, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.

出版信息

Radiother Oncol. 2019 Mar;132:236-240. doi: 10.1016/j.radonc.2018.10.007. Epub 2018 Oct 22.

DOI:10.1016/j.radonc.2018.10.007
PMID:30360998
Abstract

PURPOSE

We investigated the efficacy and safety of carbon-ion radiotherapy (C-ion RT) for locally recurrent rectal cancer (LRRC).

PATIENTS AND METHODS

Data from patients with LRRC treated with C-ion RT from November 2003 to December 2014 at three institutions were retrospectively analyzed. The endpoints of this clinical trial were overall survival (OS), local control (LC), and acute/late toxicity.

RESULTS

A total of 224 patients' data were collected. The prescribed dose was 70.4 Gy (relative biological effectiveness [RBE]-weighted absorbed dose) or 73.6 Gy (RBE) in 16 fractions. The median follow-up period from the initiation of C-ion RT was 62 months (range 6-169 months). The OS rates were 73% (95% confidence interval [CI], 67%-79%) at 3 years and 51% (95%CI 44%-58%) at 5 years. The LC rates were 93% (95%CI 88%-96%) at 3 years, and 88% (95%CI 82%-93%) at 5 years. Grade 3 acute toxicity was observed in three patients: gastrointestinal toxicity (n = 1) and pelvic infection (n = 2). Grade 3 late toxicity was observed in 12 patients: skin reaction (n = 2), gastrointestinal toxicity (n = 2), neuropathy (n = 1), and pelvic infection (n = 7). There was no grade 4 or 5 acute or late toxicity.

CONCLUSIONS

This first multi-institutional analysis of C-ion RT for LRRC indicated relatively favorable outcomes with limited toxicities.

摘要

目的

我们研究了碳离子放射疗法(C-ion RT)治疗局部复发性直肠癌(LRRC)的疗效和安全性。

方法

回顾性分析了 2003 年 11 月至 2014 年 12 月期间在三所机构接受 C-ion RT 治疗的 LRRC 患者的数据。该临床试验的终点为总生存率(OS)、局部控制率(LC)和急性/迟发性毒性。

结果

共收集了 224 例患者的数据。处方剂量为 70.4 Gy(相对生物效应[RBE]加权吸收剂量)或 73.6 Gy(RBE),共 16 个分次。从开始 C-ion RT 到中位随访时间为 62 个月(范围为 6-169 个月)。3 年时 OS 率为 73%(95%置信区间[CI],67%-79%),5 年时为 51%(95%CI 44%-58%)。3 年时 LC 率为 93%(95%CI 88%-96%),5 年时为 88%(95%CI 82%-93%)。有 3 例患者发生 3 级急性毒性:胃肠道毒性(n=1)和骨盆感染(n=2)。12 例患者发生 3 级迟发性毒性:皮肤反应(n=2)、胃肠道毒性(n=2)、神经病变(n=1)和骨盆感染(n=7)。无 4 级或 5 级急性或迟发性毒性。

结论

这是首次多机构分析 C-ion RT 治疗 LRRC 的结果,表明疗效较好,毒性有限。

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