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希罗达(卡培他滨加奥沙利铂)用于局部晚期直肠癌容积调强弧形放疗(VMAT)术前放化疗的可行性研究

[Feasibility study on Xelox (capecitabine plus oxapliplatin) in the volumetric modulated arc therapy (VMAT)-based preoperative chemoradiotherapy for locally advanced rectal cancer].

作者信息

Xiao Lin, Huang Rong, You Kaiyun, Chang Hui, Qiu Bo, Xiao Weiwei, Chen Li, Gao Yuanhong, Liu Mengzhong

机构信息

Department of Radiotherapy, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangzhou 510060, China.

出版信息

Zhonghua Wei Chang Wai Ke Za Zhi. 2014 Mar;17(3):219-24.

Abstract

OBJECTIVE

To investigate the feasibility of Xelox(capecitabine plus oxaliplatin) in the volumetric modulated arc therapy(VMAT)-based preoperative chemoradiotherapy (CRT) for locally advanced rectal cancer(LARC).

METHODS

Clinical data of 141 LARC patients in our hospital from April 2011 to April 2013 treated by preoperative CRT based on VMAT with concurrent Xelox followed by surgery were analyzed retrospectively. There were 95 men and 46 women, and the median age was 56 years old. Clinical staging was stage II( in 33 cases(18 cases with II(a, 11 cases with II(b, 4 cases with II(c) and stage III( in 108 cases(1 case with III(a, 52 cases with III(b, 55 cases with III(c). The target doses were 50 Gy for PTV1 in 25 fractions and 46 Gy for PTV2 in 23 fractions.

RESULTS

All the patients completed the planned radiotherapy, and only 2 cases were interrupted with acute grade 3 diarrhea. The overall incidence of grade 3 hematologic and non-hematologic adverse events during CRT was 9.9% and 16.3% respectively without grade 4 toxicity. Operation was performed after a median interval of 54 days(34-86 days) following CRT. The R0 resection rate was 100%, sphincter preservation rate for low rectal cancer was 45.8%(33/72), postoperative complication morbidity was 17.0%(24/141), pCR rate was 32.6%(46/141), and rates of pathological down-staging for the primary tumor, lymph node and clinical stage were 87.2%, 88% and 90.1%, respectively.

CONCLUSIONS

Xelox is feasible and well tolerated in the treatment of VMAT-based preoperative CRT for patients with LARC, with excellent rates of pCR and pathological down-staging.

摘要

目的

探讨希罗达(卡培他滨联合奥沙利铂)在容积调强弧形放疗(VMAT)基础上的局部晚期直肠癌(LARC)术前放化疗(CRT)中的可行性。

方法

回顾性分析2011年4月至2013年4月在我院接受基于VMAT的术前CRT联合希罗达治疗后行手术的141例LARC患者的临床资料。其中男性95例,女性46例,中位年龄56岁。临床分期为Ⅱ期(33例,其中Ⅱ(a)期18例、Ⅱ(b)期11例、Ⅱ(c)期4例)和Ⅲ期(108例,其中Ⅲ(a)期1例、Ⅲ(b)期52例、Ⅲ(c)期55例)。靶区剂量为PTV1 50 Gy分25次,PTV2 46 Gy分23次。

结果

所有患者均完成计划放疗,仅2例因急性3级腹泻中断治疗。CRT期间3级血液学和非血液学不良事件的总发生率分别为9.9%和16.3%,无4级毒性反应。CRT后中位间隔54天(34 - 86天)行手术。R0切除率为100%,低位直肠癌保肛率为45.8%(33/72),术后并发症发生率为17.0%(24/141),病理完全缓解(pCR)率为32.6%(46/141),原发肿瘤、淋巴结和临床分期的病理降期率分别为87.2%、88%和90.1%。

结论

希罗达用于LARC患者基于VMAT的术前CRT治疗是可行的且耐受性良好,pCR率和病理降期率优异。

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