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The chronic lymphocytic leukemia international prognostic index (CLL-IPI) predicts time to first treatment in early CLL: Independent Validation in a Prospective Cohort of Early Stage Patients

机译:慢性淋巴细胞白血病国际预后指数(CLL-IPI)预测早期CLL的首次治疗时间:在早期患者的预期队列中的独立验证

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摘要

The chronic lymphocytic leukemia International Prognostic Index (CLL-IPI) combines 5 parameters (age, clinical stage, TP53 status [normal vs. del(17p) and/or TP53 mutation], IGHV mutational status, serum β2-microglobulin) to predict survival and time-to-first-treatment (TTFT) in CLL patients. We performed an observational study in 337 prospectively collected, Binet stage A patients to validate the ability of the CLL-IPI to predict TTFT in an independent cohort of early stage CLL patients. The CLL-IPI score stratified Binet stage A patients into three subgroups with different outcome. Since the CLL-IPI was originally developed to predict survival, we next investigated the optimal cut-off score to predict TTFT in Binet stage A patients. Recursive partitioning analysis identified three subsets with scores of 0 (n=139), 1 (n=90), and ≥ 2(n=108). The probability of remaining free from therapy 5 years after diagnosis was 85%, 67% and 46% in these three categories (P<0.0001.; C-statistic:c=0.72; 95% CI:0.58–0.81). This optimized CLL-IPI scoring for TTFT was subsequently validated in an independent cohort of Binet A patients from the Mayo Clinic (n=525). The ability of either original or optimized CLL-IPI to predict TTFT was equivalent to other prognostic models specifically designed for this endpoint (2011 MDACC score and O-CLL1 score). Although originally developed to predict suvival, the CLL-IPI is useful for predicting TTFT in early stage CLL patients.
机译:慢性淋巴细胞白血病国际预后指数(CLL-IPI)结合5个参数(年龄,临床分期,TP53状态(正常vs. del(17p)和/或TP53突变),IGHV突变状态,血清β2-微球蛋白)来预测存活率和CLL患者的首次治疗时间(TTFT)。我们在337例前瞻性Binet A期患者中进行了一项观察性研究,以验证CLL-IPI在早期CLL患者的独立队列中预测TTFT的能力。 CLL-IPI评分将Binet A期患者分为三个亚组,每个亚组的结局均不同。由于CLL-IPI最初是为预测生存而开发的,因此我们接下来研究了Binet A期患者预测TTFT的最佳分界值。递归分区分析确定了三个子集,其分数分别为0(n = 139),1(n = 90)和≥2(n = 108)。在这三个类别中,诊断后5年仍无治疗的可能性分别为85%,67%和46%(P <0.0001; C统计量:c = 0.72; 95%CI:0.58–0.81)。随后在来自梅奥诊所(n = 525)的Binet A患者的独立队列中验证了针对TTFT的这种优化的CLL-IPI评分。原始的或优化的CLL-IPI预测TTFT的能力与专门为此终点设计的其他预后模型相同(2011 MDACC评分和O-CLL1评分)。尽管CLL-IPI最初是为预测suvival而开发的,但可用于预测早期CLL患者的TTFT。

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