Gattei Valter, Bulian Pietro, Del Principe Maria Ilaria, Zucchetto Antonella, Maurillo Luca, Buccisano Francesco, Bomben Riccardo, Dal-Bo Michele, Luciano Fabrizio, Rossi Francesca M, Degan Massimo, Amadori Sergio, Del Poeta Giovanni
Clinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, Istituto di Ricovero e Cura a Carattere Scientifico Aviano, Italy.
Blood. 2008 Jan 15;111(2):865-73. doi: 10.1182/blood-2007-05-092486. Epub 2007 Oct 24.
CD49d/alpha4-integrin is variably expressed in chronic lymphocytic leukemia (CLL). We evaluated its relevance as independent prognosticator for overall survival and time to treatment (TTT) in a series of 303 (232 for TTT) CLLs, in comparison with other biologic or clinical prognosticators (CD38, ZAP-70, immunoglobulin variable heavy chain (IGHV) gene status, cytogenetic abnormalities, soluble CD23, beta2-microglobulin, Rai staging). Flow cytometric detection of CD49d was stable and reproducible, and the chosen cut-off (30% CLL cells) easily discriminated CD49dlow from CD49dhigh cases. CD49d, whose expression was strongly associated with that of CD38 (P<.001) and ZAP-70 (P<.001), or with IGHV mutations (P<.001), was independent prognosticator for overall survival along with IGHV mutational status (CD49d hazard ratio, HRCD49d=3.52, P=.02; HRIGHV=6.53, P<.001) or, if this parameter was omitted, with ZAP-70 (HRCD49d=3.72, P=.002; HRZAP-70=3.32, P=.009). CD49d was also a prognosticator for TTT (HR=1.74, P=.007) and refined the impact of all the other factors. Notably, a CD49dhigh phenotype, although not changing the outcome of good prognosis (ZAP-70low, mutated IGHV) CLL, was necessary to correctly prognosticate the shorter TTT of ZAP-70high (HR=3.12; P=.023) or unmutated IGHV (HR=2.95; P=.002) cases. These findings support the introduction of CD49d detection in routine prognostic assessment of CLL patients, and suggest both pathogenetic and therapeutic implications for CD49d expression in CLL.
CD49d/α4整合素在慢性淋巴细胞白血病(CLL)中的表达存在差异。我们评估了其作为303例CLL患者(TTT分析纳入232例)总生存期和治疗时间(TTT)独立预后指标的相关性,并与其他生物学或临床预后指标(CD38、ZAP-70、免疫球蛋白可变重链(IGHV)基因状态、细胞遗传学异常、可溶性CD23、β2-微球蛋白、Rai分期)进行比较。CD49d的流式细胞术检测稳定且可重复,选定的临界值(30%的CLL细胞)能够轻松区分CD49d低表达和高表达病例。CD49d的表达与CD38(P<0.001)、ZAP-70(P<0.001)或IGHV突变(P<0.001)密切相关,它与IGHV突变状态一起是总生存期的独立预后指标(CD49d风险比,HRCD49d=3.52,P=0.02;HRIGHV=6.53,P<0.001),或者如果省略该参数,则与ZAP-70一起是独立预后指标(HRCD49d=3.72,P=0.002;HRZAP-70=3.32,P=0.009)。CD49d也是TTT的预后指标(HR=1.74,P=0.007),并细化了所有其他因素的影响。值得注意的是,CD49d高表达表型虽然不改变预后良好(ZAP-70低表达、IGHV突变)的CLL患者的结局,但对于正确预测ZAP-70高表达(HR=3.12;P=0.023)或IGHV未突变(HR=2.95;P=0.002)患者较短的TTT是必要的。这些发现支持在CLL患者的常规预后评估中引入CD49d检测,并提示CD49d在CLL中的表达具有发病机制和治疗意义。