首页> 美国卫生研究院文献>other >Phase I Study of Azacitidine following Donor Lymphocyte Infusion for Relapsed Acute Myeloid Leukemia Post Allogeneic Stem Cell Transplantation
【2h】

Phase I Study of Azacitidine following Donor Lymphocyte Infusion for Relapsed Acute Myeloid Leukemia Post Allogeneic Stem Cell Transplantation

机译:供体淋巴细胞输注后阿扎胞苷用于异基因干细胞移植后复发的急性髓细胞性白血病的I期研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Donor lymphocyte infusion (DLI) without prophylactic immunosuppression has been used for relapsed AML after allogeneic stem cell transplant (allo-SCT). However DLI is associated with an increased incidence of acute Graft vs. Host Disease (aGVHD). In mice, administration of azacitidine (AzaC) on days 4, 6, 8, and 10 post DLI increases regulatory T cell (Treg) numbers and prevents GVHD without hindering Graft vs. Leukemia (GVL). Based on these findings, we conducted a phase 1 study of AzaC post DLI for AML relapse post allo-SCT. AzaC was administered on days 4, 6, 8 and 10 post-DLI. Dose escalation was done using a 3+3 design with three AzaC dose levels: 30 mg/m2 (level -1), 45 mg/m2 (level 1) and 75 mg/m2 (level 2). Three patients were treated in the 45 mg/m2 dose level and 5 patients were treated in the 75 mg/m2 dose level; no DLTs or grade 3-5 treatment related toxicities were observed. After a median follow-up of 5.2 months, no patients developed grade III-IV aGVHD and no patients died of aGVHD. Six out of 8 patients in the treatment group responded to treatment including two cytogenetic complete remissions, one hematologic complete remission, and three complete remissions with incomplete count recovery. In conclusion, administration of AzaC early post DLI is well tolerated and can potentially prevent GVHD after DLI. Further studies are required to evaluate the effect of azacitidine early post DLI on GVHD and GVL.
机译:不进行预防性免疫抑制的供体淋巴细胞输注(DLI)已用于异基因干细胞移植(allo-SCT)后的复发性AML。但是,DLI与急性移植物抗宿主病(aGVHD)的发生率增加相关。在小鼠中,在DLI后第4、6、8和10天施用阿扎胞苷(AzaC)可增加调节性T细胞(Treg)的数量,并预防GVHD,而不会影响嫁接抗白血病(GVL)。基于这些发现,我们进行了DLI后AzaC对异源SCT后AML复发的1期研究。 DLI后第4、6、8和10天施用AzaC。剂量递增使用3 + 3设计进行,具有三个AzaC剂量水平:30 mg / m 2 (-1级),45 mg / m 2 (1级)和75 mg / m 2 (2级)。 3例接受45 mg / m 2 剂量水平的治疗,5例接受75 mg / m 2 剂量水平的治疗;没有观察到DLT或3-5级治疗相关的毒性。在中位随访5.2个月后,没有患者出现III-IV级aGVHD,也没有患者死于aGVHD。治疗组中八分之六的患者对治疗有反应,包括两次细胞遗传学完全缓解,一次血液学完全缓解和三次完全缓解,计数恢复不完全。总之,在DLI后早期给予AzaC的耐受性良好,并可能在DLI后预防GVHD。需要进一步的研究以评估DLI早期阿扎胞苷对GVHD和GVL的影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号