Department of Hematology, University Tor Vergata, Roma, Italy.
Leuk Lymphoma. 2010 Jan;51(1):95-106. doi: 10.3109/10428190903350421.
In chronic lymphocytic leukemia (CLL), inhibition of spontaneous apoptosis determines a worse prognosis and increasing evidences show that disease progression relies also upon cycling CLL cells. We investigated bcl-2, as measure of apoptosis, and CD71, as measure of proliferation, by flow cytometry in 265 patients with CLL. Combining bcl-2 with CD71 values, we defined three subgroups: (1) bcl2 - CD71-; (2) bcl2 + CD71+; and (3) bcl2 + CD71- or bcl2- CD71+. Both a shorter progression-free survival (PFS) and overall survival (OS) were observed in ZAP-70+ (p < 0.00001) and in patients with bcl2 + CD71+ (p < 0.00001 and p = 0.02). The patients with discordant in bcl2 + CD71- and bcl2- CD71+ showed an intermediate outcome. Noteworthy, patients with bcl2 + CD71+ showed a shorter PFS within ZAP-70 negative subgroup (p = 0.00009). In multivariate analysis of PFS, age (p = 0.005), beta-(2) microglobulin (B(2)-M) (p = 0.003), bcl-2 (p = 0.004), CD49d (p = 0.001), and ZAP-70 (p < 0.001) resulted to be significant prognostic factors. The independent prognostic significance of B(2)-M (p = 0.009) and bcl-2 (p = 0.03) was confirmed within ZAP-70 negative patients. Bcl-2 and CD71 can be considered as interesting progression indicators, which should be validated in an independent cohort of patients, to take timely therapeutic decisions in CLL.
在慢性淋巴细胞白血病(CLL)中,自发凋亡的抑制决定了更差的预后,越来越多的证据表明疾病的进展也依赖于循环 CLL 细胞。我们通过流式细胞术检查了 265 例 CLL 患者的 bcl-2(凋亡的标志物)和 CD71(增殖的标志物)。我们将 bcl-2 和 CD71 的值相结合,将患者分为三组:(1)bcl2-CD71-;(2)bcl2+CD71+;(3)bcl2+CD71-或 bcl2-CD71+。ZAP-70+(p<0.00001)和 bcl2+CD71+(p<0.00001 和 p=0.02)患者的无进展生存期(PFS)和总生存期(OS)均较短。bcl2+CD71-和 bcl2-CD71+不一致的患者表现出中间结果。值得注意的是,在 ZAP-70 阴性亚组中,bcl2+CD71+患者的 PFS 较短(p=0.00009)。在 PFS 的多变量分析中,年龄(p=0.005)、β-2 微球蛋白(B(2)-M)(p=0.003)、bcl-2(p=0.004)、CD49d(p=0.001)和 ZAP-70(p<0.001)是重要的预后因素。B(2)-M(p=0.009)和 bcl-2(p=0.03)在 ZAP-70 阴性患者中的独立预后意义得到了证实。Bcl-2 和 CD71 可以作为有前途的进展指标,这需要在独立的患者队列中得到验证,以便在 CLL 中及时做出治疗决策。