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放射治疗在非常年幼的横纹肌肉瘤患儿治疗中所面临的挑战。

The challenging role of radiation therapy for very young children with rhabdomyosarcoma.

作者信息

Puri Dev R, Wexler Leonard H, Meyers Paul A, La Quaglia Michael P, Healey John H, Wolden Suzanne L

机构信息

Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2006 Jul 15;65(4):1177-84. doi: 10.1016/j.ijrobp.2006.02.014. Epub 2006 May 6.

Abstract

PURPOSE

To evaluate local control and toxicity for very young children treated with multimodality therapy for rhabdomyosarcoma (RMS).

METHODS AND MATERIALS

From 1990 to 2004, 20 patients<or=36 months at diagnosis were treated at our institution. Nineteen underwent chemotherapy (CMT), surgery and/or intraoperative high-dose-rate brachytherapy (IOHDR), and external-beam radiation (EBRT). Median age was 17 months. Sites included extremity (7), trunk (5), parameningeal (4), orbit (1), head/neck (1), bladder/prostate (1). Histologies consisted of 10 embryonal (53%) and 9 alveolar/undifferentiated (47%). Ten had delayed gross total resection (GTR) at median time of 17 weeks after the start of CMT, and 8 of these underwent IOHDR. Median interval between start of CMT and EBRT was 18 weeks. Median EBRT dose was 36 Gy. EBRT technique was either intensity-modulated (11), three-dimensional (3), or two-dimensional (5). Functional outcome was assessed for patients alive>or=1 year after diagnosis (15) in terms of mild, moderate, or severe deficits.

RESULTS

Median follow-up was 33 months for survivors and 23 months for all patients. Two-year actuarial local control, event-free survival, disease-specific survival, and overall survival were 84%, 52%, 74%, and 62%, respectively. All patients who began EBRT<or=18 weeks after the start of CMT had their disease controlled locally. Five have mild deficits and 10 have no deficits.

CONCLUSIONS

A reduced dose of 36-Gy EBRT after delayed GTR may maximize local control while minimizing long-term sequelae for very young children with RMS, but unresectable tumors (e.g., parameningeal) require higher doses. Normal-tissue-sparing techniques such as intensity-modulated radiation therapy and IOHDR are encouraged. Local control may be maximized when EBRT begins <or=18 weeks after initiation of CMT, but further study is warranted. Longer follow-up is required to determine the full extent of late effects.

摘要

目的

评估接受多模式治疗的极低龄儿童横纹肌肉瘤(RMS)的局部控制情况和毒性反应。

方法和材料

1990年至2004年,本机构共治疗了20例诊断时年龄≤36个月的患者。19例接受了化疗(CMT)、手术和/或术中高剂量率近距离放疗(IOHDR)以及外照射放疗(EBRT)。中位年龄为17个月。病变部位包括四肢(7例)、躯干(5例)、脑膜旁(4例)、眼眶(1例)、头颈部(1例)、膀胱/前列腺(1例)。组织学类型包括10例胚胎型(53%)和9例肺泡型/未分化型(47%)。10例在CMT开始后中位17周时进行了延迟根治性全切除(GTR),其中8例接受了IOHDR。CMT开始至EBRT的中位间隔时间为18周。EBRT的中位剂量为36 Gy。EBRT技术包括调强放疗(11例)、三维适形放疗(3例)或二维放疗(5例)。对诊断后存活≥1年的患者(15例)的功能结局按照轻度、中度或重度功能缺陷进行评估。

结果

幸存者的中位随访时间为33个月,所有患者的中位随访时间为23个月。2年精算局部控制率、无事件生存率、疾病特异性生存率和总生存率分别为84%、52%、74%和62%。所有在CMT开始后≤18周开始EBRT的患者其疾病均获得局部控制。5例有轻度功能缺陷,10例无功能缺陷。

结论

对于极低龄RMS患儿,延迟GTR后给予36 Gy的较低EBRT剂量可能在使局部控制最大化的同时将长期后遗症最小化,但不可切除的肿瘤(如脑膜旁肿瘤)需要更高剂量。鼓励采用如调强放疗和IOHDR等正常组织保护技术。当EBRT在CMT开始后≤18周开始时局部控制可能最大化,但仍需进一步研究。需要更长时间的随访以确定远期效应的全部范围。

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