Division of Pediatric Hematology/Oncology, Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, USA.
Pediatr Blood Cancer. 2012 Sep;59(3):468-74. doi: 10.1002/pbc.23395. Epub 2011 Nov 18.
Several studies have demonstrated the prognostic utility of absolute lymphocyte count (ALC) during therapy for a range of malignancies, with low ALC associated with adverse outcome. Here we investigated whether ALC retained independent prognostic significance with respect to minimal residual disease (MRD) status in children with acute lymphoblastic leukemia (ALL).
We reviewed 171 cases of pediatric ALL treated on the Children's Oncology Group P9900 series of treatment trials. Variables analyzed included ALC at several time points during Induction, age at diagnosis, cytogenetics, initial white blood cell count, and MRD status at Day 29 of Induction (MRD-29).
We found high ALC at Induction Day 29 (ALC-29) to be an independent, clinically significant predictor of improved relapse-free and overall survival (OS). Patients with ALC-29 >1,500 cells/µl had a superior 6-year relapse-free survival (80 ± 4% vs. 62 ± 8%, P = 0.018) and overall survival (96 ± 2% vs. 74 ± 8%, P = 0.001). Moreover, ALC-29 identified distinct prognostic subgroups within cases stratified by MRD-29. In subjects with >0.01% MRD, ALC-29 > or <1,500 cells/µl had a significant 51% difference in 6-year OS (92 ± 7% vs. 41 ± 16%, P = 0.0001).
ALC, a readily obtainable test, constitutes a significant and independent prognostic factor in childhood ALL that may refine current MRD-based risk stratification algorithms and provide key prognostic information in settings where MRD determination is not feasible.
多项研究已经证明绝对淋巴细胞计数(ALC)在多种恶性肿瘤的治疗过程中的预后作用,低 ALC 与不良预后相关。在这里,我们研究了在急性淋巴细胞白血病(ALL)患儿中,ALC 是否在微小残留病(MRD)状态方面保留了独立的预后意义。
我们回顾了在儿童肿瘤学组 P9900 系列治疗试验中接受治疗的 171 例儿童 ALL 病例。分析的变量包括诱导期内的几个时间点的 ALC、诊断时的年龄、细胞遗传学、初始白细胞计数以及诱导期第 29 天的 MRD 状态(MRD-29)。
我们发现诱导期第 29 天的高 ALC(ALC-29)是无复发生存和总生存(OS)改善的独立、具有临床意义的预测因素。ALC-29 >1500 个细胞/µl 的患者具有更好的 6 年无复发生存率(80 ± 4%对 62 ± 8%,P = 0.018)和总生存率(96 ± 2%对 74 ± 8%,P = 0.001)。此外,ALC-29 在按 MRD-29 分层的病例中确定了不同的预后亚组。在 MRD >0.01%的患者中,ALC-29 >或<1500 个细胞/µl 的患者的 6 年 OS 差异有统计学意义(92 ± 7%对 41 ± 16%,P = 0.0001)。
ALC 是一种易于获得的检测方法,它是儿童 ALL 中的一个重要且独立的预后因素,它可能会完善目前基于 MRD 的风险分层算法,并在无法确定 MRD 的情况下提供关键的预后信息。