用于 GvHD 预防的 CAST 方案:CIBMTR 倾向评分匹配分析。

IF 3.6 3区 医学 Q2 HEMATOLOGY
A Samer Al-Homsi , Todd E. DeFor , Kelli Cole , Frank Cirrone , Stephanie King , Andres Suarez-Londono , George Yaghmour , Stephanie Boisclair , Caitrin Bupp , Stephen R. Spellman
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引用次数: 0

摘要

此前,我们曾报道过移植后联合使用环磷酰胺(PTCy)、阿巴西普和短程他克莫司(CAST)预防外周血单倍体移植后移植物抗宿主病(GvHD)的良好效果。为了进一步证实这些结果,我们进行了倾向得分匹配分析。采用近邻倾向得分匹配法,将参加 CAST 试验的患者与国际血液和骨髓移植研究中心(CIBMTR)数据库中接受过 PTCy、他克莫司和霉酚酸酯治疗的同期队列中的患者进行匹配。根据协变量的密度分布和标准化差异(中位数为 0.09)衡量,配对之间达到了极佳的平衡。在 +120 天时,CAST 组群的急性 GvHD II-IV 级发生率以及一年无 GvHD 和无复发生存率(GRFS)分别为 16.7% 和 66.7%,而对照组分别为 28.6% 和 47.6%。这一趋势未达到统计学意义(P= 0.14 和 0.07),可能是由于患者和事件的数量较少。另一方面,CAST 在统计学上显著降低了复发率(9.5% 对 26.2%,p=0.045),提高了无病生存率(85.7% 对 61.9%,p=0.01)。我们的数据有力地推动了在随机临床试验中对 CAST 进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CAST Regimen for GvHD Prophylaxis: A CIBMTR Propensity Score-Matched Analysis
Previously, we reported excellent results with the combination of post-transplant cyclophosphamide (PTCy), abatacept, and a short course of tacrolimus (CAST) for the prevention of graft-versus-host disease (GvHD) following peripheral blood haploidentical transplantation. To further substantiate these results, we performed a propensity score-matched analysis. Patients enrolled in the CAST trial were matched with patients from a contemporaneous cohort from the Center for International Blood and Marrow Transplant Research database who received PTCy, tacrolimus, and mycophenolate mofetil, using nearest neighbor propensity score matching. An excellent balance between pairs was achieved as measured by the density distribution and standardized differences of covariates (median 0.09). The rates of acute GvHD grades II to IV at day +120 and 1-year GvHD- and relapse-free survival were 16.7% and 66.7% in the CAST cohort versus 28.6% and 47.6% in the control group, respectively. This trend did not reach statistical significance (P = .14 and .07), possibly due to the small numbers of patients and events. On the other hand, CAST was associated with a statistically significant reduction in the incidence of relapse (9.5% versus 26.2%, P = .045) with improved disease-free survival (85.7% versus 61.9%, P = .01). Our data provides a strong impetus to examine CAST in a randomized clinical trial.
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来源期刊
CiteScore
7.00
自引率
15.60%
发文量
1061
审稿时长
51 days
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