Salit Rachel B, Oliver David C, Delaney Colleen, Sorror Mohamed L, Milano Filippo
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Department of Medicine, University of Washington Medical Center, Seattle, Washington.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Biol Blood Marrow Transplant. 2017 Apr;23(4):654-658. doi: 10.1016/j.bbmt.2017.01.084. Epub 2017 Feb 9.
The Hematopoietic Cell Transplantation Comorbidity Index (HCT-CI) has been validated as a tool for evaluating the risk of treatment-related mortality (TRM) in HLA-matched sibling and matched unrelated donor bone marrow and peripheral blood stem cell transplantation patients. However, the role of the HCT-CI after cord blood transplantation (CBT) has not been fully investigated. In this analysis, we sought to evaluate the predictive value of the HCT-CI in patients undergoing reduced-intensity conditioning (RIC) CBT. Between 2006 and 2013, HCT-CI scores were prospectively tabulated for patients with hematologic malignancies sequentially enrolled on multicenter RIC CBT studies coordinated by the Fred Hutchinson Cancer Research Center: 151 patients with acute myeloid leukemia/myelodysplastic syndrome (n = 101), chronic myeloid leukemia (n = 3), acute lymphocytic leukemia (n = 24), non-Hodgkin lymphoma (n = 8), Hodgkin lymphoma (n = 3), and other hematologic malignancies (n = 12) underwent RIC CBT and were included. Two patients received a single CBT and the remaining 149 received a double CBT. All patients received cyclosporine and mycophenolate mofetil for graft-versus-host disease prophylaxis. Median HCT-CI for the whole group was 3 (range, 0 to 8). Using the HCT-CI categories of low (0), intermediate (1 or 2), and high risk (>3), there was no significant difference in TRM between the 3 groups. However, when the patients were divided into 2 groups, HCT-CI ≤ 3 or > 3, the incidence of TRM at 3 years after transplantation was 26% (95% confidence interval [CI], 17 to 36) in the HCT-CI ≤ 3 group versus 50% (95% CI, 30 to 67) in the HCT-CI > 3 group (P = .01). Overall survival for patients with HCT-CI ≤ 3 was 40% (95% CI, 27 to 51) versus 29% in patients with HCT-CI >3 (95% CI, 12 to 48) (P = .08). Our study demonstrates that HCT-CI score > 3 is associated with an increased risk of TRM at 3 years after transplantation in patients undergoing RIC CBT. Because of the significant risk of TRM in patients with HCT-CI > 3 compared with risk for those with HCT-CI ≤ 3, patients with an HCT-CI score >3 should be counseled before undergoing RIC CBT.
造血细胞移植合并症指数(HCT-CI)已被确认为评估 HLA 配型相合的同胞及配型相合的无关供者骨髓和外周血干细胞移植患者治疗相关死亡率(TRM)风险的工具。然而,脐带血移植(CBT)后 HCT-CI 的作用尚未得到充分研究。在本分析中,我们试图评估 HCT-CI 在接受减低强度预处理(RIC)CBT 患者中的预测价值。2006 年至 2013 年期间,对在弗雷德·哈钦森癌症研究中心协调开展的多中心 RIC CBT 研究中依次入组的血液系统恶性肿瘤患者前瞻性地记录 HCT-CI 评分:151 例急性髓系白血病/骨髓增生异常综合征患者(n = 101)、慢性髓系白血病患者(n = 3)、急性淋巴细胞白血病患者(n = 24)、非霍奇金淋巴瘤患者(n = 8)、霍奇金淋巴瘤患者(n = 3)以及其他血液系统恶性肿瘤患者(n = 12)接受了 RIC CBT 并被纳入研究。2 例患者接受了单次 CBT,其余 149 例接受了双份 CBT。所有患者均接受环孢素和霉酚酸酯预防移植物抗宿主病。全组患者的 HCT-CI 中位数为 3(范围 0 至 8)。使用低风险(0)、中风险(1 或 2)和高风险(>3)的 HCT-CI 分类,三组之间的 TRM 无显著差异。然而,当将患者分为两组,HCT-CI≤3 或>3 时,移植后 3 年 HCT-CI≤3 组的 TRM 发生率为 26%(95%置信区间[CI],17%至 36%),而 HCT-CI>3 组为 50%(95%CI,30%至 67%)(P = 0.