Department of Hematology, Faculty of Medicine, University of Tsukuba, Tennodai 1-1-1, Tsukuba, Ibaraki, 305-8575, Japan.
Ann Hematol. 2021 May;100(5):1295-1301. doi: 10.1007/s00277-021-04439-6. Epub 2021 Feb 12.
Cytokine release syndrome (CRS), occurring in more than 70% of HLA-haploidentical hematopoietic stem-cell transplantations with post-transplant cyclophosphamide (PT/CY-haplo), can lead to hemodynamic instability and worsen clinical outcomes. A calcineurin inhibitor is initiated after cyclophosphamide administration in the commonly used PT/CY regimens. Here, we conducted a phase I/II, prospective, single-center trial of PT/CY-haplo to evaluate the safety and efficacy of cyclophosphamide on days 3 and 5 along with cyclosporin and mycophenolate mofetil started from day - 1. Thirty-five adults with hematologic malignancies were enrolled. Myeloablative and reduced-intensity conditioning were used in 25 and 10 patients, respectively. Graft sources were bone marrow in 11 patients and mobilized peripheral blood stem cells in 24 patients. Disease-free survival on day 100, the primary endpoint, was 86% (95% confidence interval (CI), 69-94), which was over the predefined threshold of 50%. Unexpectedly, only 20% (95% CI, 8.4-37) of patients developed fever of > 38 °C early after graft infusion, all CRS grade 1, and all of which resolved just after cyclophosphamide administration. The cumulative incidences of grades II-IV acute graft-versus-host disease (GVHD), III-IV acute GVHD, and moderate-severe chronic GVHD were 23% (95% CI, 11-38), 6% (95% CI, 1-17), and 11% (95% CI, 4-25), respectively. The 3-year overall survival rate was 49% (95% CI, 31-64). Our results suggest that administration of cyclosporine and mycophenolate mofetil prior to PT/CY can reduce the frequency and severity of CRS without increasing GVHD. UMIN Clinical Trial Registry numbers: 000006631 and 000015694.
细胞因子释放综合征(CRS)在超过 70%的 HLA 单倍体造血干细胞移植后接受移植后环磷酰胺(PT/CY-单倍体)治疗的患者中发生,可导致血流动力学不稳定并恶化临床结局。在常用的 PT/CY 方案中,环磷酰胺给药后开始使用钙调神经磷酸酶抑制剂。在此,我们进行了一项 I/II 期、前瞻性、单中心试验,评估在第 3 天和第 5 天使用环磷酰胺以及从第-1 天开始使用环孢素和霉酚酸酯的 PT/CY-单倍体的安全性和疗效。35 名血液系统恶性肿瘤患者入组。25 名患者接受清髓性和减低强度预处理,10 名患者接受减低强度预处理。移植物来源分别为骨髓 11 例和动员外周血干细胞 24 例。主要终点第 100 天无病生存率为 86%(95%可信区间[CI],69-94),超过了 50%的预设阈值。出乎意料的是,只有 20%(95%CI,8.4-37)的患者在移植后早期出现>38°C 的发热,所有患者均为 CRS 1 级,且在环磷酰胺给药后均得到缓解。2 级-4 级急性移植物抗宿主病(GVHD)、3 级-4 级急性 GVHD 和中重度慢性 GVHD 的累积发生率分别为 23%(95%CI,11-38)、6%(95%CI,1-17)和 11%(95%CI,4-25)。3 年总生存率为 49%(95%CI,31-64)。我们的结果表明,在 PT/CY 之前给予环孢素和霉酚酸酯可降低 CRS 的频率和严重程度,而不增加 GVHD。UMIN 临床试验注册编号:000006631 和 000015694。