Cervantes F, Rozman M, Rosell J, Urbano-Ispizua A, Montserrat E, Rozman C
Postgraduate School of Haematology Farreras Valenti, University of Barcelona, Spain.
Br J Haematol. 1990 Sep;76(1):27-32. doi: 10.1111/j.1365-2141.1990.tb07832.x.
In 80 patients with Ph-positive chronic myelogenous leukaemia the main clinical, haematological and cytogenetical data were recorded at diagnosis of blast crisis and evaluated for prognostic significance. At the time of the analysis 73 patients had died, with a median survival of 4-8 months from diagnosis of blast crisis for the whole series. When analysed as a time-dependent variable, the achievement of a favourable response to chemotherapy resulted in a longer patient's survival. On the other hand, the univariate analysis identified six pretreatment characteristics associated with a poorer prognosis: a longer chronic phase, presence of extramedullary blastic involvement, a platelet count below 200 x 10(9)/l, a less marked leucocytosis, a blood blast cell percentage higher than 10%, and presence of trisomy 8. The latter parameters were included in a multiple regression model together with the blast cell phenotype (lymphoid versus non-lymphoid), and only four of them (trisomy 8, duration of chronic phase, platelet count, and leucocyte count) retained their prognostic influence. When the therapeutical response was also included in the regression model, it proved to be the most important prognostic variable, followed by trisomy 8, length of chronic phase, extramedullary disease, and platelet count, whereas the leukocyte count lost its predictive value. Thus, in spite of the short overall survival of blast crisis patients, the identification of prognostic factors in such a haematological condition may be of interest, especially in the interpretation of new therapeutical approaches.
在80例Ph阳性慢性粒细胞白血病患者中,记录了原始细胞危象诊断时的主要临床、血液学和细胞遗传学数据,并评估其预后意义。分析时,73例患者已死亡,整个系列从原始细胞危象诊断起的中位生存期为4 - 8个月。当作为时间依赖性变量进行分析时,化疗取得良好反应可使患者生存期延长。另一方面,单因素分析确定了六个与预后较差相关的预处理特征:慢性期较长、存在髓外原始细胞浸润、血小板计数低于200×10⁹/L、白细胞增多不明显、血原始细胞百分比高于10%以及存在8号染色体三体。将后述参数与原始细胞表型(淋巴样与非淋巴样)一起纳入多元回归模型,其中只有四个参数(8号染色体三体、慢性期持续时间、血小板计数和白细胞计数)保留了其预后影响。当治疗反应也纳入回归模型时,它被证明是最重要的预后变量,其次是8号染色体三体、慢性期长度、髓外疾病和血小板计数,而白细胞计数失去了其预测价值。因此,尽管原始细胞危象患者的总体生存期较短,但在这种血液学疾病中识别预后因素可能是有意义的,特别是在解释新的治疗方法时。