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ZAP-70与CD38联合分析在慢性淋巴细胞白血病中的预后意义

Prognostic significance of combined analysis of ZAP-70 and CD38 in chronic lymphocytic leukemia.

作者信息

D'Arena Giovanni, Tarnani Michela, Rumi Carlo, Vaisitti Tiziana, Aydin Semra, De Filippi Rosaria, Perrone Francesco, Pinto Antonio, Chiusolo Patrizia, Deaglio Silvia, Malavasi Fabio, Laurenti Luca

机构信息

Hematology Oncology Unit, National Cancer Institute, Fondazione G. Pascale, Via Mariano Semmola, Naples, Italy.

出版信息

Am J Hematol. 2007 Sep;82(9):787-91. doi: 10.1002/ajh.20936.

Abstract

The clinical heterogeneity that characterizes chronic lymphocytic leukemia (CLL) poses critical questions concerning the identification of high risk patients. Unmutated IgV(H) genes, CD38 and ZAP-70 expression have emerged as the most useful tools in identifying aggressive CLL. The simultaneous expression of ZAP-70 and CD38 in 157 patients with CLL has been evaluated. Fifty-seven patients (36%) were positive for ZAP-70 and 46 patients (29%) were positive for CD38. Both molecules were highly correlated and predictive of the clinical course of the disease. According to the simultaneous evaluation of ZAP-70 and CD38, patients were divided into three groups. In 81 patients (52%), there was a negative concordance of both molecules (ZAP-70(-)/CD38(-)); in 27 patients (17%) there was a positive concordance (ZAP-70(+)/CD38(+)); in 49 patients (31%) there was a discordant expression (ZAP-70(+)/CD38(-) and ZAP-70(-)/CD38(+)). A comparison of the clinical and laboratory data showed in ZAP-70(+)/CD38(+) patients a significantly higher bone marrow and peripheral blood lymphocytosis, lower hemoglobin levels, more advanced clinical stage, and higher number of unmutated IgV(H) status with respect to the other two groups. Furthermore, ZAP-70(+)/CD38(+) patients displayed a much shorter treatment-free interval (median 12 months vs 42 months in discordant patients and not reached in ZAP-70(-)CD38(-) patients). These results prove that the concomitant evaluation of ZAP-70 and CD38 expression allows the separation of CLL patients in prognostic subgroups and suggest that their simultaneous assessment should become an integral component of the CLL diagnostic grid.

摘要

慢性淋巴细胞白血病(CLL)所具有的临床异质性给高危患者的识别带来了关键问题。未突变的IgV(H)基因、CD38和ZAP-70表达已成为识别侵袭性CLL最有用的工具。对157例CLL患者中ZAP-70和CD38的同时表达情况进行了评估。57例患者(36%)ZAP-70呈阳性,46例患者(29%)CD38呈阳性。这两种分子高度相关且可预测疾病的临床进程。根据ZAP-70和CD38的同时评估结果,患者被分为三组。81例患者(52%)两种分子均为阴性一致性(ZAP-70(-)/CD38(-));27例患者(17%)为阳性一致性(ZAP-70(+)/CD38(+));49例患者(31%)为不一致表达(ZAP-70(+)/CD38(-)和ZAP-70(-)/CD38(+))。临床和实验室数据比较显示,与其他两组相比,ZAP-70(+)/CD38(+)患者的骨髓和外周血淋巴细胞增多更为显著,血红蛋白水平更低,临床分期更晚,未突变IgV(H)状态的比例更高。此外,ZAP-70(+)/CD38(+)患者的无治疗间期明显更短(中位数为12个月,而不一致患者为42个月,ZAP-70(-)CD38(-)患者未达到)。这些结果证明,同时评估ZAP-70和CD38表达可将CLL患者分为不同的预后亚组,并表明它们的同时评估应成为CLL诊断流程中不可或缺的一部分。

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