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Pushing the envelope—nonmyeloablative and reduced intensity preparative regimens for allogeneic hematopoietic transplantation

机译:推波助澜—同种异体造血移植的非清髓性和降低强度的制备方案

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摘要

Allogeneic hematopoietic cell transplantation (HCT) was originally developed to allow delivery of myeloablative doses of chemotherapy and radiotherapy. With better understanding of disease pathophysiology, the graft vs malignancy (GVM) effect of allogeneic hematopoietic transplantation and toxicities associated with myeloablative conditioning (MAC) regimens, the focus shifted to developing less toxic conditioning regimens to reduce treatment-related morbidity without compromising survival. Although HCT with MAC is preferred to reduced intensity conditioning (RIC) for most patients ≤ 60 years with AML/myelodysplastic syndrome and ALL, RIC and nonmyeloablative (NMA) regimens allow HCT for many otherwise ineligible patients. Reduced intensity preparative regimens have produced high rates of PFS for diagnoses, which are highly sensitive to GVM. Relapse of the malignancy is the major cause of treatment failure with RIC/NMA HCT. Incorporation of novel agents like bortezomib or lenalidomide, addition of cellular immunotherapy and use of targeted radiation therapies could further improve outcome. In this review, we discuss commonly used RIC/NMA regimens and promising novel regimens.
机译:异基因造血细胞移植(HCT)最初是为了允许进行清髓性剂量的化学疗法和放射疗法而开发的。随着对疾病病理生理学,同种异体造血移植的移植物对恶性肿瘤(GVM)效果以及与清髓性调理(MAC)方案相关的毒性的更好了解,重点转移到开发毒性更小的调理方案以减少与治疗相关的发病率而不损害生存率。尽管对于大多数≤60岁的AML /骨髓增生异常综合征和ALL患者,MAC首选HCT优于降低强度条件治疗(RIC),但RIC和非清髓(NMA)方案可使许多其他不符合条件的患者接受HCT。强度降低的制备方案产生了较高的PFS诊断率,对GVM高度敏感。 RIC / NMA HCT导致恶性肿瘤复发是治疗失败的主要原因。合并硼替佐米或来那度胺等新型药物,添加细胞免疫疗法以及使用靶向放射疗法可进一步改善治疗效果。在这篇综述中,我们讨论了常用的RIC / NMA疗法和有前途的新颖疗法。

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  • 作者

    SR Pingali; RE Champlin;

  • 作者单位
  • 年(卷),期 -1(50),9
  • 年度 -1
  • 页码 1157–1167
  • 总页数 28
  • 原文格式 PDF
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