Department of Internal Medicine I, München Klinik Schwabing, Munich, Germany.
Institute of Medical Statistics and Epidemiology, Technical University Munich, Munich, Germany.
Leukemia. 2020 Apr;34(4):1038-1051. doi: 10.1038/s41375-020-0727-y. Epub 2020 Feb 10.
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.
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。