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调强放疗联合缩野推量用于儿童头颈部横纹肌肉瘤的治疗

Intensity-modulated radiotherapy with use of cone-down boost for pediatric head-and-neck rhabdomyosarcoma.

作者信息

McDonald Mark W, Esiashvili Natia, George Bradley A, Katzenstein Howard M, Olson Thomas A, Rapkin Louis B, Marcus Robert B

机构信息

Department of Radiation Oncology, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2008 Nov 1;72(3):884-91. doi: 10.1016/j.ijrobp.2008.01.058. Epub 2008 May 1.

Abstract

PURPOSE

To report our initial experience using intensity-modulated radiotherapy (IMRT) with a cone-down boost for pediatric head-and-neck rhabdomyosarcoma (RMS).

METHODS AND MATERIALS

A review of institutional treatment records identified children treated with IMRT for head-and-neck RMS between January 2000 and February 2007. All patients had undergone chemotherapy according to cooperative group RMS protocols. The initial planning target volume (PTV) covered the prechemotherapy tumor extent with variable margins, generally 1-2 cm. The boost PTV covered the postchemotherapy tumor volume, usually with a margin of 0.5-1 cm.

RESULTS

A total of 20 patients were treated with IMRT for head-and-neck RMS. Of these 20 patients, 4 had Group II, 15 Group III, and 1 Group IV disease. The site was parameningeal in 12, nonparameningeal in 6, and orbit primary in 2. Of the 20 patients, 14 were treated with a cone-down boost after a median dose of 36 Gy (range, 30-45.6). The mean initial PTV was 213.5 cm(3), and the mean boost PTV was 76.9 cm(3). Patients received a median total dose of 50.4 Gy. The median follow-up time was 29 months. The 3-year Kaplan-Meier local control rate was 100%, although 1 patient developed an in-field recurrence 50 months after IMRT. The 3-year event-free survival rate, overall survival rate, and risk of central nervous system failure was 74%, 76%, and 7%, respectively.

CONCLUSIONS

Our preliminary follow-up of pediatric head-and-neck RMS patients treated with IMRT revealed excellent local control. The initial targeting of the prechemotherapy tumor volume with 1-2-cm margin to 30.6 or 36 Gy followed by a cone-down boost to the postchemotherapy tumor volume with a 0.5-1-cm margin allowed for significant sparing of normal tissues and provided good local control.

摘要

目的

报告我们使用调强放射治疗(IMRT)联合缩野加量治疗儿童头颈部横纹肌肉瘤(RMS)的初步经验。

方法和材料

回顾机构治疗记录,确定2000年1月至2007年2月期间接受IMRT治疗头颈部RMS的儿童。所有患者均按照协作组RMS方案接受了化疗。初始计划靶体积(PTV)覆盖化疗前肿瘤范围,边界可变,一般为1 - 2厘米。加量PTV覆盖化疗后肿瘤体积,通常边界为0.5 - 1厘米。

结果

共有20例患者接受IMRT治疗头颈部RMS。这20例患者中,4例为Ⅱ组,15例为Ⅲ组,1例为Ⅳ组疾病。病变部位位于脑膜旁12例,非脑膜旁6例,眼眶原发2例。20例患者中,14例在中位剂量36 Gy(范围30 - 45.6)后接受缩野加量。初始PTV平均为213.5立方厘米,加量PTV平均为76.9立方厘米。患者接受的中位总剂量为50.4 Gy。中位随访时间为29个月。3年Kaplan - Meier局部控制率为100%,尽管1例患者在IMRT后50个月出现野内复发。3年无事件生存率、总生存率和中枢神经系统衰竭风险分别为74%、76%和7%。

结论

我们对接受IMRT治疗的儿童头颈部RMS患者的初步随访显示局部控制良好。以1 - 2厘米边界对化疗前肿瘤体积进行初始靶区勾画至30.6或36 Gy,随后以0.5 - 1厘米边界对化疗后肿瘤体积进行缩野加量,可显著减少正常组织受量并提供良好的局部控制。

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