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SIB-IMRT在肛管癌中的临床经验及选择性文献综述

Clinical experience of SIB-IMRT in anal cancer and selective literature review.

作者信息

Janssen Stefan, Glanzmann Christoph, Bauerfeind Peter, Stieb Sonja, Studer Gabriela, Brown Michelle, Riesterer Oliver

机构信息

Departments of Radiation Oncology, University Hospital Zurich, Rämistrasse 100, CH-8091 Zurich, Switzerland.

出版信息

Radiat Oncol. 2014 Sep 8;9:199. doi: 10.1186/1748-717X-9-199.

DOI:10.1186/1748-717X-9-199
PMID:25199879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4261589/
Abstract

PURPOSE

To evaluate feasibility and outcome of our institutional SIB-IMRT schedule in patients with anal cancer and to selectively review the literature on different SIB-IMRT schedules.

PATIENTS AND METHODS

Between 01/08-06/13 25 patients with biopsy proven squamous cell anal cancer were treated in our institution with IMRT. Radiotherapy was delivered in two series using a SIB-IMRT schedule of 45 Gy/1.8 Gy to the primary tumor and adjacent pelvic lymph nodes and 38 Gy/1.52 Gy to elective nodes followed by an IMRT boost of 7×2 Gy = 14 Gy to the primary tumor and involved nodes (cumulative prescription dose: 59 Gy).

RESULTS

Mean follow-up was 20 months (range: 4-68). The 2-year-local control, colostomy-free survival, distant metastases-free survival and overall survival rates were 92%, 92%, 92%, and 88%, respectively. Grade 3 acute skin toxicity was observed in 6 patients (24%). No high grade gastrointestinal or urinary acute toxicity occurred. Four patients required more than one day of treatment interruption due to acute toxicity. No grade 3 or higher late sequelae were observed.

CONCLUSION

We present our institutional SIB-IMRT experience treating patients with anal cancer in two series using moderate single doses from 1.5-2.0 Gy. Our results, in terms of loco-regional outcome and toxicity, were comparable to other studies. The incidence of treatment interruptions was very low. Therefore this schedule appears to be safe for clinical use.

摘要

目的

评估我院采用同步整合加量调强放疗(SIB-IMRT)方案治疗肛管癌患者的可行性及疗效,并选择性回顾不同SIB-IMRT方案的相关文献。

患者与方法

2008年1月至2013年6月期间,我院对25例经活检证实为鳞状细胞肛管癌的患者进行了调强放疗。放疗分两个疗程进行,采用SIB-IMRT方案,对原发肿瘤及邻近盆腔淋巴结给予45 Gy/1.8 Gy的剂量,对选择性淋巴结给予38 Gy/1.52 Gy的剂量,随后对原发肿瘤及受累淋巴结给予7×2 Gy = 14 Gy的调强放疗推量(累积处方剂量:59 Gy)。

结果

平均随访时间为20个月(范围:4 - 68个月)。2年局部控制率、无结肠造口生存率、无远处转移生存率和总生存率分别为92%、92%、92%和88%。6例患者(24%)出现3级急性皮肤毒性。未发生高级别胃肠道或泌尿系统急性毒性。4例患者因急性毒性需要中断治疗超过1天。未观察到3级或更高等级的晚期后遗症。

结论

我们介绍了我院采用1.5 - 2.0 Gy的中等单次剂量分两个疗程治疗肛管癌患者的SIB-IMRT经验。我们在局部区域疗效和毒性方面的结果与其他研究相当。治疗中断的发生率非常低。因此,该方案似乎可安全用于临床。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a48/4261589/5aafd510adab/13014_2013_1176_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a48/4261589/6cc85532c162/13014_2013_1176_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a48/4261589/5aafd510adab/13014_2013_1176_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a48/4261589/6cc85532c162/13014_2013_1176_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a48/4261589/5aafd510adab/13014_2013_1176_Fig2_HTML.jpg

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