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慢性淋巴细胞白血病与幼淋巴细胞白血病的关系。IV. 生存及预后特征分析。

The relationship between chronic lymphocytic leukaemia and prolymphocytic leukaemia. IV. Analysis of survival and prognostic features.

作者信息

Melo J V, Catovsky D, Gregory W M, Galton D A

出版信息

Br J Haematol. 1987 Jan;65(1):23-9. doi: 10.1111/j.1365-2141.1987.tb06130.x.

Abstract

The prognostic value of biological, clinical and laboratory features was analysed in a series of 265 patients with chronic lymphocytic leukaemia (CLL) and prolymphocytic leukaemia (PLL). On univariate analysis seven features were shown to influence significantly the survival of the whole group of patients: absolute prolymphocyte count (ABS PROL), percentage of prolymphocytes (%PROL), WBC, spleen size, age, intensity of surface-membrane immunoglobulin (SmIg) and mouse (M) rosettes. Multivariate regression analysis of these features showed that only ABS PROL and spleen size had independent prognostic significance. The survival in PLL (38 cases) was significantly shorter than in CLL (227 cases) (median survival = 3 and 8 years, respectively). Patients with CLL with an increased %PROL (11-55%), defined as CLL/PL, could be divided into two groups: those with ABS PROL less than or equal to 15 X 10(9)/l (26 cases) fell within the 'standard-prognostic risk' for typical CLL (i.e. less than or equal to 10% PROL), whereas the survival outlook for the cases with ABS PROL greater than 15 X 10(9)/l (40 cases) was as bad as for PLL. A scoring system was generated with the four features that showed high prognostic significance: ABS PROL, spleen size, SmIg and M-rosettes. The score proved to be superior to any single feature as a predictor of survival, being especially useful in the analysis of the CLL/PL group: cases with high scores (greater than 2) had a median survival of 2.5 years, while the median has not been reached for those with low scores (less than or equal to 2). We suggest that this scoring system may help to identify the cases of CLL/PL that behave as PLL, and as such may benefit from different treatment.

摘要

对265例慢性淋巴细胞白血病(CLL)和幼淋巴细胞白血病(PLL)患者的生物学、临床和实验室特征的预后价值进行了分析。单因素分析显示,有七个特征对整个患者组的生存有显著影响:幼淋巴细胞绝对计数(ABS PROL)、幼淋巴细胞百分比(%PROL)、白细胞计数(WBC)、脾脏大小、年龄、表面膜免疫球蛋白(SmIg)强度和小鼠(M)玫瑰花结。对这些特征进行多变量回归分析表明,只有ABS PROL和脾脏大小具有独立的预后意义。PLL患者(38例)的生存期明显短于CLL患者(227例)(中位生存期分别为3年和8年)。%PROL升高(11%-55%)的CLL患者,即CLL/PL患者,可分为两组:ABS PROL小于或等于15×10⁹/L的患者(26例)属于典型CLL的“标准预后风险”(即PROL小于或等于10%),而ABS PROL大于15×10⁹/L的患者(40例)的生存前景与PLL患者一样差。利用具有高预后意义的四个特征建立了一个评分系统:ABS PROL、脾脏大小、SmIg和M玫瑰花结。该评分作为生存预测指标被证明优于任何单一特征,在分析CLL/PL组时特别有用:高分(大于2)患者的中位生存期为2.5年,而低分(小于或等于2)患者的中位生存期尚未达到。我们认为,这个评分系统可能有助于识别表现为PLL的CLL/PL病例,因此可能从不同的治疗中获益。

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