Palmer M K, Hann I M, Jones P M, Evans D I
Br J Cancer. 1980 Dec;42(6):841-9. doi: 10.1038/bjc.1980.331.
Thirty-two variables at diagnosis of acute lymphoblastic leukaemia (ALL) were studied in an unselected population-bases series of 209 children. Twelve variables had individually a statistically significant effect on the duration of first remission. A multivariate analysis using data on the 199 children who went into complete remission showed that all significant variation in remission times could be explained by only 3 variables acting simultaneously. These were the total white blood count (WBC) at diagnosis, the Franco-American-British (FAB) classification of blast morphology and the percentage of lymphoblasts with PAS+ coarse granules or blocks. A simple scoring system (for WBC add 1 if less than 20 X 10(9)/1, add 2 if 20 - 50 X 10(9)/1, add 3 if greater than or equal to 50 X 10(9)/1; for L2 or L3 leukaemia add 1; for PAS+ less than 5% add 1) separated patients into risk groups with widely different median lengths of first remission. Application of the risk score improves the prediction of the outcome of treatment, and the clinical trials, allows more accurate stratification, less extensive data collection and simpler analysis.
在一项基于209名儿童的非选择性人群系列研究中,对急性淋巴细胞白血病(ALL)诊断时的32个变量进行了研究。12个变量各自对首次缓解期的持续时间有统计学上的显著影响。对进入完全缓解的199名儿童的数据进行多变量分析表明,缓解时间的所有显著差异仅可由同时起作用的3个变量来解释。这3个变量分别是诊断时的白细胞总数(WBC)、原始细胞形态的法美英(FAB)分类以及具有PAS + 粗大颗粒或块状物的淋巴母细胞百分比。一个简单的评分系统(若WBC小于20×10⁹/L加1分,20 - 50×10⁹/L加2分,大于或等于50×10⁹/L加3分;L2或L3白血病加1分;PAS + 小于5%加1分)将患者分为首次缓解期中位数长度差异很大的风险组。风险评分的应用改善了对治疗结果的预测,并且在临床试验中,可实现更准确的分层、减少广泛的数据收集并简化分析。