Paulino A C
Department of Radiotherapy, Loyola University of Chicago, Stritch School of Medicine, Maywood, Illinois, USA.
Cancer Invest. 1999;17(3):223-30. doi: 10.3109/07357909909021426.
Radiation therapy plays a crucial role in the management of children with parameningeal rhabdomyosarcomas. Because of the close proximity to the skull base, most lesions are not amenable to complete surgical resection without mutilation, and treatment has primarily been chemoradiation. Adequate radiotherapy dose, coverage of the tumor, and knowledge of potential areas of invasion are of paramount importance as demonstrated by early data from the Intergroup Rhabdomyosarcoma Study Group. The timing, dose, and treatment volume for parameningeal rhabdomyosarcomas have evolved in the last 25 years in a continuous effort to find ways of maximizing local control while reducing possible late sequelae. Hyperfractionated radiation therapy is currently being tested against conventional dose radiation therapy for group III tumors. At present, approximately 70% of children treated for parameningeal rhabdomyosarcoma on the Intergroup Rhabdomyosarcoma Study are alive at 5 years compared with a 25% survival before the formation of multi-institutional cooperative group studies.
放射治疗在儿童脑膜旁横纹肌肉瘤的治疗中起着至关重要的作用。由于靠近颅底,大多数病变在不造成毁容的情况下无法进行完整的手术切除,治疗主要是放化疗。如横纹肌肉瘤研究组的早期数据所示,足够的放疗剂量、肿瘤覆盖范围以及对潜在浸润区域的了解至关重要。在过去25年中,脑膜旁横纹肌肉瘤的放疗时机、剂量和治疗体积不断演变,一直在努力寻找在减少可能的晚期后遗症的同时最大化局部控制的方法。目前正在针对III组肿瘤对超分割放疗与传统剂量放疗进行对比试验。目前,在横纹肌肉瘤研究组接受脑膜旁横纹肌肉瘤治疗的儿童中,约70%在5年后存活,而在多机构合作组研究形成之前,生存率为25%。