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前瞻性 II 期研究:高危急性髓系白血病和骨髓增生异常综合征患者接受异基因造血干细胞移植后,预防性使用低剂量阿扎胞苷和供者淋巴细胞输注。

Prospective phase II study of prophylactic low-dose azacitidine and donor lymphocyte infusions following allogeneic hematopoietic stem cell transplantation for high-risk acute myeloid leukemia and myelodysplastic syndrome.

机构信息

Hematology Department, Nantes University Hospital, Nantes, France.

Cancer Research Center Nantes-Angers, INSERM U1232, Nantes, France.

出版信息

Bone Marrow Transplant. 2019 Nov;54(11):1815-1826. doi: 10.1038/s41409-019-0536-y. Epub 2019 May 14.

Abstract

Thirty patients, with high-risk acute myeloid leukemia (AML, n = 20) or myelodysplastic syndrome (MDS, n = 10), were enrolled in a phase II trial entailing prophylactic post-transplant azacitidine (AZA) plus escalated doses of donor lymphocyte infusion (DLI). The median number of AZA cycles was 5 (1-12) with 10 patients (33%) completing the 12 projected cycles. DLI were performed in 17 patients: 5 received one DLI, 2 received 2 DLI and 8 received 3 infusions. AZA was well tolerated, but discontinued in 20 patients primarily due to graft-versus-host disease (GvHD) and relapse. The cumulative incidence (CI) of grade 1-3 acute GvHD was 31.5% and the chronic GvHD CI was 53% at 2 years. At a median follow-up of 49 months (27-63), 18 patients are alive. The overall and disease-free survivals are 65.5% (CI 95% = 48.2-82.8) at 2 years. Cause of death was mainly relapse for 9 patients. The median time to relapse was 7 months (2.5-58) and the cumulative incidence of relapse at 2 years was 27.6% (CI 95% = 12.8-44.6). These results confirm that AZA is well tolerated as a prophylactic treatment to reduce the risk of post-transplantation relapse and compared favorably to those of patients who receive no post-transplant maintenance.

摘要

30 名高危急性髓系白血病(AML,n=20)或骨髓增生异常综合征(MDS,n=10)患者入组了一项涉及预防性移植后阿扎胞苷(AZA)加递增剂量供者淋巴细胞输注(DLI)的 II 期试验。中位 AZA 周期数为 5(1-12),10 例患者(33%)完成了 12 个预期周期。在 17 例患者中进行了 DLI:5 例接受了 1 次 DLI,2 例接受了 2 次 DLI,8 例接受了 3 次输注。AZA 耐受性良好,但主要由于移植物抗宿主病(GvHD)和复发而停用。1-3 级急性 GvHD 的累积发生率(CI)为 31.5%,2 年时慢性 GvHD 的 CI 为 53%。在中位随访 49 个月(27-63)时,18 例患者存活。2 年时的总生存率和无病生存率分别为 65.5%(CI 95%=48.2-82.8)。9 例患者的死亡原因为主要复发。复发的中位时间为 7 个月(2.5-58),2 年时的复发累积发生率为 27.6%(CI 95%=12.8-44.6)。这些结果证实,AZA 作为一种预防性治疗药物耐受性良好,可降低移植后复发的风险,并且与未接受移植后维持治疗的患者相比具有优势。

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