Coldman A J, Fryer C J, Elwood J M, Sonley M J
Cancer. 1980 Oct 15;46(8):1896-1901. doi: 10.1002/1097-0142(19801015)46:8<1896::aid-cncr2820460833>3.0.co;2-y.
A study of a consecutive series of 99 children with neuroblastoma seen at two major Toronto hospitals between 1951 and 1971 is reported. The children who were aged 24 months or less at diagnosis showed an overall two-year survival rate of 59 percent. Analysis, including fitting of a log-linear model, showed that increased probability of survival was associated with younger age at onset, nonadrenal site, and lower staging and the each of these factors acted independently. The sex of the child had no prognostic effect. This study thus extends earlier work by demonstrating the independent prognostic influence of site of tumor. The implications for treatment policy are discussed.
报告了一项对1951年至1971年间在多伦多两家主要医院就诊的99例连续性神经母细胞瘤患儿的研究。诊断时年龄在24个月及以下的患儿,其总体两年生存率为59%。分析(包括对数线性模型拟合)表明,生存概率增加与发病年龄较小、非肾上腺部位、较低分期相关,且这些因素各自独立起作用。患儿的性别对预后无影响。本研究通过证明肿瘤部位的独立预后影响,扩展了早期的研究工作。文中还讨论了对治疗策略的影响。