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婴幼儿软组织肉瘤管理的创新:高剂量率近距离放射疗法

Innovation in the management of soft tissue sarcomas in infants and young children: high-dose-rate brachytherapy.

作者信息

Nag S, Martínez-Monge R, Ruymann F, Jamil A, Bauer C

机构信息

Arthur G. James Cancer Hospital and Research Institute, Columbus, OH, USA.

出版信息

J Clin Oncol. 1997 Sep;15(9):3075-84. doi: 10.1200/JCO.1997.15.9.3075.

Abstract

PURPOSE

Conventional low-dose-rate (LDR) brachytherapy is effective in treating childhood sarcomas, but often not practical (due to the associated radiation hazards) in the young children who require continuous observation and sedation. Fractionated high-dose-rate brachytherapy (HDR) was used to deliver adequate tumoricidal radiation while preserving bone and organ growth in children.

MATERIALS AND METHODS

Twelve children with diverse sarcomas were treated with fractionated HDR. The median age at diagnosis was 18 months (range, 1 to 42). Nine patients had rhabdomyosarcoma and three had other soft tissue sarcoma (STS) variants. Ten patients had microscopic residual disease at the time of brachytherapy. All patients were treated with appropriate chemotherapy and surgery. HDR was delivered in 3-Gy fractions twice a day to a total dose of 36 Gy in 8 days. External-beam radiation therapy (EBRT) was avoided. Patients were monitored for a median of 61 months (range, 30 to 78).

RESULTS

One patient developed local recurrence and distant metastases to the lungs. The 6-year actuarial local control and overall survival rates were 91% and 81%, respectively. Brachytherapy-related morbidity occurred in 50% of patients. The morbidity was mild to moderate in 42% of patients and consisted primarily of acute skin and mucosal reaction. One patient experienced severe (grade III to IV) toxicity. Another child, treated to the tongue, had delayed dentition only in the teeth adjacent to the brachytherapy site. The other children have exhibited only minimal or none of the bone growth retardation expected with EBRT.

CONCLUSION

The combination of conservative surgery, chemotherapy, and exclusive HDR to postchemotherapy tumor volume with a modest margin, avoiding EBRT, provided disease control in carefully selected young children, while preserving bone growth and organ function. The short duration of therapy and small volume irradiated allowed chemotherapy to be resumed shortly after brachytherapy. The use of HDR challenges the present philosophy of radiotherapy treatment volume, which holds that the prechemotherapy tumor volume should be treated with an acceptable margin. Brachytherapy should be included in multicentric clinical trials in young children.

摘要

目的

传统低剂量率(LDR)近距离放射治疗对儿童肉瘤有效,但对于需要持续观察和镇静的幼儿来说往往不实用(由于相关的辐射危害)。分次高剂量率近距离放射治疗(HDR)用于在保留儿童骨骼和器官生长的同时提供足够的杀瘤辐射。

材料与方法

12例患有不同肉瘤的儿童接受了分次HDR治疗。诊断时的中位年龄为18个月(范围1至42个月)。9例患者患有横纹肌肉瘤,3例患有其他软组织肉瘤(STS)变体。10例患者在近距离放射治疗时存在显微镜下残留病灶。所有患者均接受了适当的化疗和手术。HDR以3Gy的分次剂量每天两次给药,8天内总剂量达36Gy。避免了外照射放疗(EBRT)。患者的中位随访时间为61个月(范围30至78个月)。

结果

1例患者出现局部复发和肺远处转移。6年精算局部控制率和总生存率分别为91%和81%。50%的患者发生了与近距离放射治疗相关 的并发症。42%的患者并发症为轻至中度,主要包括急性皮肤和黏膜反应。1例患者出现严重(III至IV级)毒性反应。另一名接受舌部治疗的儿童仅在近距离放射治疗部位相邻的牙齿出现出牙延迟。其他儿童仅表现出极少或未出现EBRT预期的骨骼生长迟缓。

结论

在精心挑选的幼儿中,保守手术、化疗以及对化疗后肿瘤体积给予适度边缘的单纯HDR联合治疗,避免EBRT,可实现疾病控制,同时保留骨骼生长和器官功能。治疗持续时间短和照射体积小使得近距离放射治疗后不久即可恢复化疗。HDR的使用对当前放疗靶区的理念提出了挑战,当前理念认为应在化疗前肿瘤体积周围给予可接受的边缘进行治疗。近距离放射治疗应纳入针对幼儿的多中心临床试验。

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