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CLL 国际预后指数可预测单克隆 B 细胞淋巴增生和 Rai 0 期 CLL 的结果。

The CLL International Prognostic Index predicts outcomes in monoclonal B-cell lymphocytosis and Rai 0 CLL.

机构信息

Division of Hematology, Department of Medicine and.

Division of Biomedical Statistics & Informatics, Mayo Clinic, Rochester, MN.

出版信息

Blood. 2021 Jul 15;138(2):149-159. doi: 10.1182/blood.2020009813.

Abstract

The utility of the chronic lymphocytic leukemia-international prognostic index (CLL-IPI) in predicting outcomes of individuals with Rai 0 stage CLL and monoclonal B-cell lymphocytosis (MBL) is unclear. We identified 969 individuals (415 MBL and 554 Rai 0 CLL; median age, 64 years; 65% men) seen at Mayo Clinic between 1 January 2001 and 1 October 2018, and ascertained time to first therapy (TTFT) and overall survival (OS). After a median follow up of 7 years, the risk of disease progression needing therapy was 2.9%/y for MBL (median, not reached) and 5%/y for Rai 0 CLL (median, 10.4 years). Among patients with low, intermediate, and high/very high-risk CLL-IPI risk groups, the estimated 5-year risk of TTFT was 13.5%, 30%, and 58%, respectively, P< .0001 (c-statistic = 0.69); and the estimated 5-year OS was 96.3%, 91.5%, and 76%, respectively, P< .0001 (c-statistic = 0.65). In a multivariable analysis of absolute B-cell count with individual factors of the CLL-IPI, the absolute B-cell count was associated with shorter TTFT (hazard ratio [HR] for each 10 × 109/L increase: 1.31; P< .0001) and shorter OS (HR: 1.1; P = .02). The OS of the entire cohort was similar to that of the age- and sex-matched general population of Minnesota (P = .17), although Rai 0 CLL patients with high and very high-risk CLL-IPI score had significantly shorter OS (P= .01 and P= .0001, respectively). The results of this study demonstrate the ability of CLL-IPI to predict time from diagnosis to first treatment (an end point not affected by therapy) in a large cohort of patients whose only manifestation of disease is a circulating clonal lymphocyte population.

摘要

慢性淋巴细胞白血病国际预后指数(CLL-IPI)在预测 Rai 0 期 CLL 和单克隆 B 细胞淋巴增生症(MBL)患者结局中的作用尚不清楚。我们在梅奥诊所确定了 969 名患者(415 名 MBL 和 554 名 Rai 0 CLL;中位年龄 64 岁;65%为男性),这些患者于 2001 年 1 月 1 日至 2018 年 10 月 1 日就诊,并确定了首次治疗时间(TTFT)和总生存期(OS)。中位随访 7 年后,MBL 的疾病进展需要治疗的风险为 2.9%/y(中位未达到),Rai 0 CLL 的风险为 5%/y(中位 10.4 年)。在低、中、高/极高风险 CLL-IPI 风险组的患者中,估计 5 年 TTFT 的风险分别为 13.5%、30%和 58%,P<.0001(c 统计量=0.69);估计 5 年 OS 分别为 96.3%、91.5%和 76%,P<.0001(c 统计量=0.65)。在 CLL-IPI 个体因素与绝对 B 细胞计数的多变量分析中,绝对 B 细胞计数与 TTFT 缩短相关(每增加 10×109/L 的风险比[HR]:1.31;P<.0001)和 OS 缩短相关(HR:1.1;P=.02)。整个队列的 OS 与明尼苏达州年龄和性别匹配的一般人群相似(P=.17),尽管 Rai 0 CLL 患者的 CLL-IPI 评分高和极高风险患者的 OS 明显缩短(P=.01 和 P=.0001)。这项研究的结果表明,CLL-IPI 能够预测从诊断到首次治疗的时间(不受治疗影响的终点),这在一大群仅表现为循环克隆淋巴细胞群体的患者中是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bcc/8288657/7731cf60902f/bloodBLD2020009813absf1.jpg

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