Ninane J, Pritchard J, Malpas J S
Arch Dis Child. 1981 Jul;56(7):544-8. doi: 10.1136/adc.56.7.544.
Between 1970 and 1977, 69 children with newly diagnosed stage III or IV neuroblastoma were treated with pulses of either cyclophosphamide and vincristine (CV) (n = 23), or cyclophosphamide, vincristine, and adriamycin (CVA) (n = 46). The 'complete' and partial response rates were 35 and 22% to CV, and 43 and 26% to CVA. For 'complete' responders the median time to relapse was 18 months for those treated with CV, and 17 months for those treated CVA; for partial responders the times were 5 and 7 months respectively. At 2 1/2 years only 17% of the CV patients and only 13% of the CVA patients were alive and free of disease, giving a 15% overall survival rate. The addition of adriamycin to cyclophosphamide and vincristine did not significantly improve the response rate, duration of response, or survival in these children with advanced neuroblastoma. The previously noted favourable effects of age less than 1 year at diagnosis and of female sex were confirmed. The equally poor survival for stage III and stage IV patients justifies the inclusion of stage III patients in a bad prognosis group.
1970年至1977年间,69例新诊断为Ⅲ期或Ⅳ期神经母细胞瘤的患儿接受了环磷酰胺和长春新碱(CV)(n = 23)或环磷酰胺、长春新碱和阿霉素(CVA)(n = 46)的脉冲治疗。CV组的“完全”缓解率和部分缓解率分别为35%和22%,CVA组为43%和26%。对于“完全”缓解者,接受CV治疗的患者复发的中位时间为18个月,接受CVA治疗的患者为17个月;对于部分缓解者,时间分别为5个月和7个月。在2年半时,CV组仅17%的患者和CVA组仅13%的患者存活且无疾病,总生存率为15%。在环磷酰胺和长春新碱的基础上加用阿霉素并未显著提高这些晚期神经母细胞瘤患儿的缓解率、缓解持续时间或生存率。之前提到的诊断时年龄小于1岁及女性性别所具有的有利影响得到了证实。Ⅲ期和Ⅳ期患者同样较差的生存率证明将Ⅲ期患者纳入预后不良组是合理的。