Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts.
Am J Hematol. 2014 Jun;89(6):591-7. doi: 10.1002/ajh.23695. Epub 2014 Mar 3.
To determine whether outcome after allogeneic hematopoietic cell transplantation (HCT) could be estimated by using peripheral white blood cell count (WBC) as a metric that integrates several aspects of HCT recovery, we conducted a retrospective study of 1,109 adult patients who underwent first allogeneic HCT from 2003 through 2009. WBC at 1-3 months after HCT was categorized as low (<2), normal (2-10), and high (>10 × 10(9) cells/L). Overall survival (OS) and progression-free survival (PFS) were lower for patients with low or high WBC at 1-3 months after HCT (P < 0.0001). We developed a predictive three-group risk model based on the pattern of WBC recovery early after HCT. Five-year OS was 47, 30, and 15% (P < 0.0001) and 5-year PFS was 39, 22, and 14% for patients in the three different risk groups (P < 0.0001). The pattern of WBC recovery early after HCT provides prognostic information for relapse, nonrelapse mortality, progression-free survival, and overall survival. A scoring system based on the trajectory of the WBC in the first 3 months after HCT can effectively stratify patients into three groups with different PFS and OS. If validated, this system could be useful in the clinical management of patients after HCT, and to stratify patients enrolled on HCT clinical trials.
为了确定外周血白细胞计数(WBC)是否可以作为一种综合评估造血细胞移植(HCT)恢复多个方面的指标来预测异基因 HCT 后的结果,我们对 2003 年至 2009 年间接受首次异基因 HCT 的 1109 例成年患者进行了回顾性研究。HCT 后 1-3 个月的 WBC 分为低(<2)、正常(2-10)和高(>10×10(9)细胞/L)。HCT 后 1-3 个月 WBC 低或高的患者总生存率(OS)和无进展生存率(PFS)较低(P<0.0001)。我们根据 HCT 后早期 WBC 恢复模式制定了一个预测性的三组风险模型。5 年 OS 分别为 47%、30%和 15%(P<0.0001),5 年 PFS 分别为 39%、22%和 14%,三组患者的 PFS 和 OS 差异有统计学意义(P<0.0001)。HCT 后早期 WBC 恢复模式为复发、非复发死亡率、无进展生存率和总生存率提供了预后信息。基于 HCT 后前 3 个月 WBC 轨迹的评分系统可以有效地将患者分为三组,每组的 PFS 和 OS 不同。如果得到验证,该系统可能有助于 HCT 后患者的临床管理,并对 HCT 临床试验中的患者进行分层。