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随机 III 期 BMT CTN 试验:在血液恶性肿瘤的清髓性造血细胞移植中,钙调神经磷酸酶抑制剂免费的慢性移植物抗宿主病干预。

Randomized Phase III BMT CTN Trial of Calcineurin Inhibitor-Free Chronic Graft-Versus-Host Disease Interventions in Myeloablative Hematopoietic Cell Transplantation for Hematologic Malignancies.

机构信息

Johns Hopkins Medical Center, Baltimore, MD.

Medical College of Wisconsin, Milwaukee, WI.

出版信息

J Clin Oncol. 2022 Feb 1;40(4):356-368. doi: 10.1200/JCO.21.02293. Epub 2021 Dec 2.

Abstract

PURPOSE

Calcineurin inhibitors (CNI) are standard components of graft-versus-host disease (GVHD) prophylaxis after hematopoietic cell transplantation (HCT). Prior data suggested that CNI-free approaches using donor T-cell depletion, either by ex vivo CD34 selection or in vivo post-transplant cyclophosphamide (PTCy) as a single agent, are associated with lower rates of chronic GVHD (cGVHD).

METHODS

This multicenter phase III trial randomly assigned patients with acute leukemia or myelodysplasia and an HLA-matched donor to receive CD34-selected peripheral blood stem cell, PTCy after a bone marrow (BM) graft, or tacrolimus and methotrexate after BM graft (control). The primary end point was cGVHD (moderate or severe) or relapse-free survival (CRFS).

RESULTS

Among 346 patients enrolled, 327 received HCT, 300 per protocol. Intent-to-treat rates of 2-year CRFS were 50.6% for CD34 selection (hazard ratio [HR] compared with control, 0.80; 95% CI, 0.56 to 1.15; = .24), 48.1% for PTCy (HR, 0.86; 0.61 to 1.23; = .41), and 41.0% for control. Corresponding rates of overall survival were 60.1% (HR, 1.74; 1.09 to 2.80; = .02), 76.2% (HR, 1.02; 0.60 to 1.72; = .95), and 76.1%. CD34 selection was associated with lower moderate to severe cGVHD (HR, 0.25; 0.12 to 0.52; = .02) but higher transplant-related mortality (HR, 2.76; 1.26 to 6.06; = .01). PTCy was associated with comparable cGVHD and survival outcomes to control, and a trend toward lower disease relapse (HR, 0.52; 0.28 to 0.96; = .037).

CONCLUSION

CNI-free interventions as performed herein did not result in superior CRFS compared with tacrolimus and methotrexate with BM. Lower rates of moderate and severe cGVHD did not translate into improved survival.

摘要

目的

钙调神经磷酸酶抑制剂(CNI)是造血细胞移植(HCT)后移植物抗宿主病(GVHD)预防的标准组成部分。先前的数据表明,使用供体 T 细胞耗竭的无 CNI 方法,通过体外 CD34 选择或体内移植后环磷酰胺(PTCy)作为单一药物,与较低的慢性 GVHD(cGVHD)发生率相关。

方法

这项多中心 III 期试验随机分配急性白血病或骨髓增生异常患者和 HLA 匹配的供体接受 CD34 选择的外周血干细胞、骨髓(BM)移植物后 PTCy 或 BM 移植物后他克莫司和甲氨蝶呤(对照)。主要终点是 cGVHD(中度或重度)或无复发存活(CRFS)。

结果

在纳入的 346 名患者中,327 名接受了 HCT,300 名按方案接受了 HCT。CD34 选择的 2 年 CRFS 意向治疗率为 50.6%(与对照组相比,风险比 [HR],0.80;95%CI,0.56 至 1.15; =.24),PTCy 为 48.1%(HR,0.86;0.61 至 1.23; =.41),对照组为 41.0%。总生存的相应率为 60.1%(HR,1.74;1.09 至 2.80; =.02)、76.2%(HR,1.02;0.60 至 1.72; =.95)和 76.1%。CD34 选择与较低的中度至重度 cGVHD 相关(HR,0.25;0.12 至 0.52; =.02),但与移植相关的死亡率较高(HR,2.76;1.26 至 6.06; =.01)。PTCy 与对照组的 cGVHD 和生存结果相当,且疾病复发率呈降低趋势(HR,0.52;0.28 至 0.96; =.037)。

结论

与 BM 中的他克莫司和甲氨蝶呤相比,本文中进行的无 CNI 干预并未导致 CRFS 更高。中度和重度 cGVHD 发生率较低并未转化为生存改善。

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