Ferrari Andrea, Casanova Michela
Istituto Nazionale Tumori, Via G.Venezian, 1-20133 Milan, Italy.
Expert Rev Anticancer Ther. 2005 Apr;5(2):283-94. doi: 10.1586/14737140.5.2.283.
Rhabdomyosarcoma is a typical tumor of childhood and adolescence. Over the years there has been a gradual but important improvement in survival for patients with this tumor, despite its high grade of malignancy. These results are due to multidisciplinary treatment approaches including surgery, radiotherapy and especially chemotherapy. Rhabdomyosarcoma is a highly chemosensitive neoplasm, and the role of this therapeutic approach has also been clearly demonstrated in the adjuvant setting. This review covers current concepts on chemotherapy for rhabdomyosarcoma, with an overview of the results of the main clinical trials conducted over recent years and considerations of possible strategies for the near future. Recommendations for adult patients with rhabdomyosarcoma are also discussed, suggesting that these patients should be treated according to pediatric guidelines.
横纹肌肉瘤是儿童和青少年时期的典型肿瘤。多年来,尽管这种肿瘤恶性程度高,但患者的生存率有了逐步且重要的提高。这些成果归功于多学科治疗方法,包括手术、放疗,尤其是化疗。横纹肌肉瘤是一种对化疗高度敏感的肿瘤,这种治疗方法在辅助治疗中的作用也已得到明确证实。本综述涵盖了横纹肌肉瘤化疗的当前概念,概述了近年来进行的主要临床试验结果,并对近期可能的策略进行了思考。还讨论了针对成年横纹肌肉瘤患者的建议,表明这些患者应按照儿科指南进行治疗。