Department of Internal Medicine, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan.
Biol Blood Marrow Transplant. 2019 Aug;25(8):1682-1688. doi: 10.1016/j.bbmt.2019.01.024. Epub 2019 Jan 30.
The overall composite of graft-versus-host disease (GVHD)-free, relapse-free survival (GRFS), defined as survival free of grade III-IV acute GVHD (aGVHD), chronic GVHD (cGVHD) requiring systemic immunosuppressive therapy (IST), or relapse, has emerged as a useful composite in clinical trials and to capture clinically meaningful events that impact quantity and quality of survival after allogeneic hematopoietic cell transplantation (HCT). We reviewed 565 consecutive patients aged ≥18 years undergoing HCT for hematologic malignancy to analyze how baseline incidence, specifics of clinical definitions, and proposed reductions in any one individual event may dynamically alter the overall performance of the composite To determine the relative impact of each GRFS event (excluding death), we accounted for competing risks using Fine and Gray methods, and correlated each event with overall survival (OS) using Kaplan-Meier methods. The consequences of modulating individual or composite endpoints on OS, such as hypothesized reductions of events of an HCT interventional trial, were examined using Monte Carlo simulations. The median age of the cohort was 54 years (range, 18 to 73 years). The majority of patients received HLA-matched unrelated donor HCT (53%), consisting of peripheral blood stem cell grafts (90%) after myeloablative conditioning (68%). Relapse conferred the greatest risk for death (hazard ratio [HR], 7.89; 95% confidence interval [CI], 5.83 to 10.69), followed by grade III-IV aGVHD (HR, 6.16; 95% CI, 4.42 to 8.56) and cGVHD requiring IST (HR, 1.69; 95% CI, 1.16 to 2.46). The overall GRFS composite correlated with an HR of 4.81 (95% CI, 3.61 to 6.41), which was lower compared with either relapse or grade III-IV aGVHD. Statistical simulations found that modulating the combined risk of both relapse and grade III-IV aGVHD predicted the greatest change in 5-year OS. These simulations suggest that GRFS as currently defined may be less optimal for correlating with OS, and further refinement of composite endpoints is needed. Nonetheless, composite endpoints may be particularly helpful in mitigating potential difficulties in interpretation when competing risks are present, most commonly seen in HCT studies.
无复发生存(GRFS)是指无 III-IV 级急性移植物抗宿主病(aGVHD)、无慢性移植物抗宿主病(cGVHD)需要系统性免疫抑制治疗(IST)或无复发的生存,作为一种有用的综合指标已在临床试验中出现,并用于捕捉影响异基因造血细胞移植(HCT)后生存数量和质量的有临床意义的事件。我们回顾了 565 例年龄≥18 岁的接受血液恶性肿瘤 HCT 的连续患者,以分析基线发生率、临床定义的具体情况,以及减少任何单一事件如何动态改变综合指标的整体性能。为了确定每个 GRFS 事件(不包括死亡)的相对影响,我们使用 Fine 和 Gray 方法考虑了竞争风险,并使用 Kaplan-Meier 方法将每个事件与总生存(OS)相关联。使用蒙特卡罗模拟研究了改变单个或综合终点对 OS 的影响,例如假设减少 HCT 干预试验的事件。该队列的中位年龄为 54 岁(范围 18 至 73 岁)。大多数患者接受 HLA 匹配的无关供体 HCT(53%),其中 90%是经过清髓性预处理(68%)后的外周血干细胞移植。复发是死亡的最大风险因素(危险比 [HR],7.89;95%置信区间 [CI],5.83 至 10.69),其次是 III-IV 级 aGVHD(HR,6.16;95% CI,4.42 至 8.56)和需要 IST 的 cGVHD(HR,1.69;95% CI,1.16 至 2.46)。总体 GRFS 复合指标与 HR 为 4.81(95% CI,3.61 至 6.41)相关,与复发或 III-IV 级 aGVHD 相比,这一比值较低。统计模拟发现,调节复发和 III-IV 级 aGVHD 的综合风险预测了 5 年 OS 的最大变化。这些模拟表明,目前定义的 GRFS 与 OS 的相关性可能不太理想,需要进一步改进综合终点。尽管如此,复合终点在存在竞争风险时(最常见于 HCT 研究中),可能特别有助于减轻解释上的潜在困难。