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B细胞慢性淋巴细胞白血病样淋巴细胞增多症无症状患者预后因素的前瞻性研究:11×10⁹/L单克隆淋巴细胞的临界值能更好地识别具有不同预后的亚组。

Prospective study of prognostic factors in asymptomatic patients with B-cell chronic lymphocytic leukemia-like lymphocytosis: the cut-off of 11 × 10(9)/L monoclonal lymphocytes better identifies subgroups with different outcomes.

作者信息

Oliveira A C, Fernández de Sevilla A, Domingo A, De La Banda E, Domingo-Domènech E, Mercadal S, Ruiz-Xivillé N, Alonso E, Encuentra M, González-Barca E

机构信息

Department of Clinical Hematology, Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Gran Vía 199-203, Hospitalet, 08908, Barcelona, Spain,

出版信息

Ann Hematol. 2015 Apr;94(4):627-32. doi: 10.1007/s00277-014-2263-1. Epub 2014 Dec 5.

Abstract

The arbitrary threshold of 5 × 10(9)/L chronic lymphocytic leukemia (CLL)-like lymphocytes differentiates monoclonal B lymphocytosis (MBL) from CLL. There are no prospective studies that search for the optimal cut-off of monoclonal lymphocytes able to predict outcome and simultaneously analyze the prognostic value of classic, immunophenotypic, and cytogenetic variables in patients with asymptomatic clonal CLL lymphocytosis (ACL), which includes MBL plus Rai 0 CLL patients. From 2003 to 2010, 231 ACL patients were enrolled in this study. Patients with 11q deletion and atypical lymphocyte morphology at diagnosis had shorter progression-free survival (PFS) (p = 0.007 and p = 0.015, respectively) and treatment-free survival (TFS) (p = 0.009 and p = 0.017, respectively). Elevated beta-2 microglobulin (B2M) also correlated with worse TFS (p = 0.002). The optimal threshold of monoclonal lymphocytes independently correlated with survival was 11 × 10(9)/L (p = 0.000 for PFS and p = 0.016 for TFS). As conclusion, monoclonal lymphocytosis higher than 11 × 10(9)/L better identifies two subgroups of patients with different outcomes than the standard cut-off value of 5 × 10(9)/L. Atypical lymphocyte morphology, 11q deletion and elevated B2M had a negative impact on the survival in ACL patients.

摘要

5×10⁹/L 这一任意阈值用于区分慢性淋巴细胞白血病(CLL)样淋巴细胞导致的单克隆 B 淋巴细胞增多症(MBL)与 CLL。目前尚无前瞻性研究探寻能够预测预后的单克隆淋巴细胞的最佳临界值,同时分析无症状克隆性 CLL 淋巴细胞增多症(ACL,包括 MBL 加 Rai 0 期 CLL 患者)患者中经典、免疫表型和细胞遗传学变量的预后价值。2003 年至 2010 年,231 例 ACL 患者纳入本研究。诊断时存在 11q 缺失和非典型淋巴细胞形态的患者无进展生存期(PFS)较短(分别为 p = 0.007 和 p = 0.015),无治疗生存期(TFS)也较短(分别为 p = 0.009 和 p = 0.017)。β2 微球蛋白(B2M)升高也与较差的 TFS 相关(p = 0.002)。与生存独立相关的单克隆淋巴细胞的最佳阈值为 11×10⁹/L(PFS 的 p = 0.000,TFS 的 p = 0.016)。结论是,与 5×10⁹/L 的标准临界值相比,高于 11×10⁹/L 的单克隆淋巴细胞增多症能更好地识别出具有不同预后的两组患者。非典型淋巴细胞形态、11q 缺失和 B2M 升高对 ACL 患者的生存有负面影响。

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