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Binet 分期 A 期初诊 CLL 患者的预后模型:德国 CLL 研究组多中心前瞻性 CLL1 试验的结果。

Prognostic model for newly diagnosed CLL patients in Binet stage A: results of the multicenter, prospective CLL1 trial of the German CLL study group.

机构信息

Department of Internal Medicine I, München Klinik Schwabing, Munich, Germany.

Institute of Medical Statistics and Epidemiology, Technical University Munich, Munich, Germany.

出版信息

Leukemia. 2020 Apr;34(4):1038-1051. doi: 10.1038/s41375-020-0727-y. Epub 2020 Feb 10.

Abstract

The heterogeneity of early stage CLL challenges prognostication, and refinement of prognostic indices for risk-adapted management in this population is essential. The aim of the multicenter, prospective CLL1 trial was to explore a novel prognostic model (CLL1-PM) developed to identify risk groups, separating patients with favorable from others with dismal prognosis. A cohort of 539 clinically, biochemically, and genetically characterized Binet stage A patients were observed until progression, first-line treatment, or death. Multivariate analysis identified six independent factors associated with overall survival (OS) and time-to-first treatment (TTFT): del(17p), unmutated IGHV, del(11q), ß2-microglobulin >3.5 mg/dL, lymphocyte doubling time (LDT) <12 months, and age >60 years. These factors were integrated into the CLL1-PM, which stratified patients into four risk groups. The CLL1-PM was prognostic for OS and TTFT, e.g., the risk of treatment at 5 years was 85.9, 51.8, 27.6, and 11.3% for very low (0-1.5), low (2-4), high (4.5-6.5), and very high-risk (7-14) scores, respectively (P < 0.001). Notably, in addition to factors comprising CLL-IPI, we substantiated del(11q) and LDT as prognostic factors in early CLL. Altogether, our findings would be useful to effectively stratify Binet stage A patients, particularly within the scope of clinical trials evaluating novel agents.

摘要

早期 CLL 的异质性对预后具有挑战性,因此对于该人群,进行风险适应管理的预后指数的精细化非常重要。多中心、前瞻性 CLL1 试验的目的是探索一种新的预后模型(CLL1-PM),以识别风险组,将预后良好的患者与预后不良的患者区分开来。该队列包括 539 名临床、生化和遗传特征明确的 Binet 分期 A 患者,直至进展、一线治疗或死亡。多变量分析确定了与总生存期(OS)和首次治疗时间(TTFT)相关的六个独立因素:del(17p)、未突变 IGHV、del(11q)、β2-微球蛋白>3.5mg/dL、淋巴细胞倍增时间(LDT)<12 个月和年龄>60 岁。这些因素被整合到 CLL1-PM 中,该模型将患者分为四个风险组。CLL1-PM 对 OS 和 TTFT 具有预后意义,例如,5 年治疗风险分别为非常低(0-1.5)、低(2-4)、高(4.5-6.5)和非常高风险(7-14)评分组的 85.9%、51.8%、27.6%和 11.3%(P<0.001)。值得注意的是,除了构成 CLL-IPI 的因素外,我们还证实了 del(11q)和 LDT 是早期 CLL 的预后因素。总之,我们的研究结果将有助于有效分层 Binet 分期 A 患者,特别是在评估新型药物的临床试验范围内。

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