Steinhorn S C
Cancer Treat Rep. 1984 Jul-Aug;68(7-8):953-8.
Improvements in survival were observed among white children less than 15 years of age diagnosed with acute lymphocytic leukemia (ALL) between 1973 and 1978 in nine of the areas covered by the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) Program. Significant increases were noted between the 3-year survival rate for children diagnosed in 1973-1975 (59%) and the rate for those diagnosed in 1976-1978 (74%). The 5-year survival rate for children diagnosed with ALL in 1973-1975 was nearly 50%. Survival of female children exceeded that for males, and younger children 1-4 years of age diagnosed with ALL had a better prognosis than older children 5-14 years of age. Both sexes and age groups showed increases in survival between 1973-1975 and 1976-1978. Improvements in survival during these time periods were not observed for children diagnosed with acute granulocytic (myelogenous) leukemia. Between 1973 and 1979, the age-adjusted incidence rate for all childhood leukemias remained fairly constant in the SEER areas, ranging from 3.7 per 100,000 population less than 15 years of age in 1973 to 3.5 per 100,000 in 1979. Reflecting observed improvements in childhood leukemia survival, the corresponding mortality rates fell from 2.2 to 1.7 per 100,000 in this same time period.
在国家癌症研究所监测、流行病学和最终结果(SEER)项目覆盖的九个地区,1973年至1978年期间,15岁以下被诊断为急性淋巴细胞白血病(ALL)的白人儿童的生存率有所提高。1973 - 1975年诊断的儿童3年生存率为59%,1976 - 1978年诊断的儿童3年生存率为74%,显著提高。1973 - 1975年被诊断为ALL的儿童5年生存率接近50%。女童的生存率超过男童,1 - 4岁被诊断为ALL的年幼儿童比5 - 14岁的年长儿童预后更好。1973 - 1975年至1976 - 1978年期间,男女和各年龄组的生存率均有所提高。被诊断为急性粒细胞(髓细胞)白血病的儿童在这些时间段内生存率没有提高。1973年至1979年,SEER地区所有儿童白血病的年龄调整发病率保持相当稳定,从1973年每10万15岁以下人口中的3.7例到1979年的3.5例。反映出儿童白血病生存率的提高,同期相应的死亡率从每10万中的2.2例降至1.7例。