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一项关于阿扎胞苷联合粒细胞-巨噬细胞集落刺激因子作为维持治疗,用于异基因血液或骨髓移植后高危急性髓系白血病(AML)或骨髓增生异常综合征(MDS)患者的 II 期研究。

A phase II study of azacitidine in combination with granulocyte-macrophage colony-stimulating factor as maintenance treatment, after allogeneic blood or marrow transplantation in patients with poor-risk acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS).

机构信息

Hematologic Malignancies and Bone Marrow Transplantation Program, Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

SSM Medical Group, St. Charles, MO, USA.

出版信息

Leuk Lymphoma. 2021 Dec;62(13):3181-3191. doi: 10.1080/10428194.2021.1948029. Epub 2021 Jul 21.

Abstract

Relapse is the most common cause of treatment failure following allogeneic blood or marrow transplantation (alloBMT) for AML or MDS. Post-transplant maintenance therapies may prevent relapse. We conducted a phase II trial combining azacitidine (AZA) with GM-CSF in non-relapsed, post-transplant patients with AML or MDS. Patients received escalating doses of AZA to a maximum of 75 mg/m for 5 days per cycle for up to 12 cycles. GM-CSF was given on days 1-10 of each cycle. Eighteen patients were treated following non-myeloablative (17) and myeloablative (1) alloBMT for AML (61.1%), MDS (27.7%), or therapy-related myeloid neoplasm (11.1%). The majority of patients (72%) received their graft from an HLA-haploidentical donor. The treatment was well-tolerated with rare grade 3-4 hematologic toxicities. One patient suffered an exacerbation of GVHD. The 24-month relapse-free and overall survivals were 47 and 57%, respectively, with a median of 18.6 and 29 months.

摘要

复发是异基因血液或骨髓移植(alloBMT)治疗 AML 或 MDS 后治疗失败的最常见原因。移植后维持治疗可能预防复发。我们进行了一项 II 期临床试验,将阿扎胞苷(AZA)与 GM-CSF 联合用于非复发、移植后 AML 或 MDS 患者。患者接受递增剂量的 AZA,每个周期最多 75mg/m2,连续 5 天,最多 12 个周期。GM-CSF 在每个周期的第 1-10 天给予。18 例患者在非清髓性(17 例)和清髓性(1 例)alloBMT 后接受治疗,用于 AML(61.1%)、MDS(27.7%)或治疗相关髓系肿瘤(11.1%)。大多数患者(72%)接受 HLA 半相合供体的移植物。治疗耐受性良好,仅有罕见的 3-4 级血液学毒性。1 例患者发生 GVHD 加重。24 个月无复发生存率和总生存率分别为 47%和 57%,中位无复发生存期和总生存期分别为 18.6 个月和 29 个月。

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