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