Pratt C B, Hustu H O, Kumar A P, Johnson W W, Ransom J L, Howarth C B, George S L
Natl Cancer Inst Monogr. 1981 Apr(56):93-101.
Between March 1962 and December 1978, 153 children with rhabdomyosarcoma (RMS) received treatment at St. Jude Children's Research Hospital. As of January 1979, 62 of these patients were still alive. Between 1962 and 1968, 20 patients were not treated by protocol, and, between 1968 and 1979, another 13 have been registered as "nonprotocol"; 6 of these 33 patients survive. Since 1968, 120 patients received treatment by 3 stage-related, multiple-modality programs. In the first protocol, chemotherapy consisted of vincristine, cyclophosphamide, and dactinomycin; 14 of 34 patients have survived after 6 to more than 10 years. In the second treatment program, which used adriamycin in addition to the 3 drugs cited above, 20 of 56 subjects remain free of disease after more than 2 to 5.5 years; toxicity of the multiple agents given in combination with radiotherapy proved intolerable and led to a modified 4-agent protocol for patients admitted since early 1977. Of 30 in this latter group, 22 are alive. Forty of 44 patients who remained free of RMS for more than 2 years continue to survive.
1962年3月至1978年12月期间,153例横纹肌肉瘤(RMS)患儿在圣裘德儿童研究医院接受治疗。截至1979年1月,其中62例患者仍存活。1962年至1968年期间,20例患者未按方案治疗,1968年至1979年期间,另有13例被登记为“未按方案治疗”;这33例患者中有6例存活。自1968年以来,120例患者通过3个与分期相关的多模式方案接受治疗。在第一个方案中,化疗药物包括长春新碱、环磷酰胺和放线菌素;34例患者中有14例在6年至10年以上后存活。在第二个治疗方案中,除上述3种药物外还使用了阿霉素,56例受试者中有20例在2年以上至5.5年后仍无疾病;与放疗联合使用的多种药物的毒性被证明难以耐受,因此从1977年初开始对入院患者采用改良的4药方案。后一组30例患者中有22例存活。44例无RMS超过2年的患者中有40例继续存活。