Havers W, Schmitt G, Stollmann B
Helv Paediatr Acta. 1979;34(5):449-58.
From 1974 to 1978, 21 children with rhabdomyosarcoma were treated in a combined interdisciplinary protocol. All children received a polychemotherapy for 18 months. Radiotherapy and surgery were used according to the stage and localization of the tumor. The overall two-year survival rate is 86 +/- 9%, the tumor free survival rate is 78 +/- 11%. 7 patients have no evidence of disease after the end of treatment.
1974年至1978年期间,21名横纹肌肉瘤患儿按照综合多学科方案接受治疗。所有患儿均接受了18个月的多药化疗。根据肿瘤的分期和部位采用放疗和手术治疗。两年总生存率为86±9%,无瘤生存率为78±11%。7名患者在治疗结束后无疾病迹象。