Blood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Blood Adv. 2021 Nov 23;5(22):4549-4559. doi: 10.1182/bloodadvances.2021005286.
Prior clinical trials largely considered prednisone 1 mg/kg per day with or without calcineurin inhibitor as standard initial therapy for chronic graft-versus-host disease (cGVHD), but uncertainty remains regarding the extent of practice variation and whether this affects subsequent outcomes. We assembled a cohort of 745 patients with cGVHD treated with initial systemic immune suppressive (IS) therapy from 3 prior cGVHD Consortium observational studies. Initial therapy was defined as first IS therapy started for cGVHD or prednisone increased to ≥0.4 mg/kg per day from lower doses within 30 days before cGVHD diagnosis to any time afterward. Initial therapies were nonprednisone IS therapies (n = 137, 18%), prednisone alone (n = 411, 55%), or prednisone plus other IS therapy (n = 197, 26%). In multivariate analysis, initial therapy group was not associated with failure-free survival (FFS; a composite of death, relapse, and new IS therapy), overall survival (OS), or nonrelapse mortality (NRM). Among the prednisone-based approaches, steroid dose was <0.25 (9%), 0.25 to 0.74 (36%), 0.75 to 1.25 (42%), or >1.25 mg/kg per day (13%). Prednisone dose within the patients treated with steroids was not significantly associated with FFS, OS, or NRM. No significant interactions were detected between overall cGVHD severity and either initial therapy group or prednisone dose for the outcomes of FFS, OS, or NRM. These observational data document heterogeneity in more contemporary cGVHD initial treatment practices, including prednisone dose and use of nonsteroid approaches. This variation was not associated with FFS, OS, or NRM. Prospective trials are needed to verify efficacy of reduced-dose prednisone or prednisone-free initial therapy approaches.
先前的临床试验主要考虑泼尼松 1mg/kg/天联合或不联合钙调磷酸酶抑制剂作为慢性移植物抗宿主病(cGVHD)的标准初始治疗,但对于实践差异的程度以及这是否会影响后续结果仍存在不确定性。我们汇集了来自三个先前的 cGVHD 联盟观察性研究的 745 例接受初始系统性免疫抑制(IS)治疗的 cGVHD 患者队列。初始治疗定义为 cGVHD 开始的首次 IS 治疗,或在 cGVHD 诊断前 30 天内从较低剂量开始将泼尼松增加至≥0.4mg/kg/天,或此后任何时间开始的治疗。初始治疗方案为非泼尼松 IS 治疗(n=137,18%)、泼尼松单药治疗(n=411,55%)或泼尼松联合其他 IS 治疗(n=197,26%)。多变量分析显示,初始治疗组与无失败生存(FFS;死亡、复发和新的 IS 治疗的综合指标)、总生存(OS)或非复发死亡率(NRM)无关。在基于泼尼松的治疗方法中,泼尼松剂量<0.25(9%)、0.25-0.74(36%)、0.75-1.25(42%)或>1.25mg/kg/天(13%)。接受激素治疗的患者中泼尼松剂量与 FFS、OS 或 NRM 均无显著相关性。未发现总体 cGVHD 严重程度与初始治疗组或泼尼松剂量之间存在显著相互作用,这与 FFS、OS 或 NRM 的结果相关。这些观察性数据记录了更现代的 cGVHD 初始治疗实践中的异质性,包括泼尼松剂量和非甾体治疗方法的应用。这种变化与 FFS、OS 或 NRM 无关。需要前瞻性试验来验证减少剂量的泼尼松或无泼尼松初始治疗方法的疗效。