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造血细胞移植和免疫效应细胞治疗的适应证:美国移植和细胞治疗学会指南。

Indications for Hematopoietic Cell Transplantation and Immune Effector Cell Therapy: Guidelines from the American Society for Transplantation and Cellular Therapy.

机构信息

Hematopoietic Malignancy & Cellular Therapy Program, West Virginia University, Morgantown, West Virginia.

Blood & Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.

出版信息

Biol Blood Marrow Transplant. 2020 Jul;26(7):1247-1256. doi: 10.1016/j.bbmt.2020.03.002. Epub 2020 Mar 9.

Abstract

The American Society for Transplantation and Cellular Therapy (ASTCT) published its first white paper on indications for autologous and allogeneic hematopoietic cell transplantation (HCT) in 2015. It was identified at the time that periodic updates of indications would be required to stay abreast with state of the art and emerging indications and therapy. In recent years the field has not only seen an improvement in transplantation technology, thus widening the therapeutic scope of HCT, but additionally a whole new treatment strategy using modified immune effector cells, including chimeric antigen receptor T cells and engineered T-cell receptors, has emerged. The guidelines review committee of the ASTCT deemed it optimal to update the ASTCT recommendations for indications for HCT to include new data and to incorporate indications for immune effector cell therapy (IECT) where appropriate. The guidelines committee established a multiple stakeholder task force consisting of transplant experts, payer representatives, and a patient advocate to provide guidance on indications for HCT and IECT. This article presents the updated recommendations from the ASTCT on indications for HCT and IECT. Indications for HCT/IECT were categorized as (1) Standard of care, where indication is well defined and supported by evidence; (2) Standard of care, clinical evidence available, where large clinical trials and observational studies are not available but have been shown to be effective therapy; (3) Standard of care, rare indication, for rare diseases where demonstrated effectiveness exists but large clinical trials and observational studies are not feasible; (4) Developmental, for diseases where preclinical and/or early-phase clinical studies show HCT/IECT to be a promising treatment option; and (5) Not generally recommended, where available evidence does not support the routine use of HCT/IECT. The ASTCT will continue to periodically review these guidelines and update them as new evidence becomes available.

摘要

美国移植与细胞治疗学会(ASTCT)于 2015 年首次发布了自体和同种异体造血细胞移植(HCT)适应证的白皮书。当时确定,为了跟上技术的最新进展和新兴的适应证和治疗方法,需要定期更新适应证。近年来,该领域不仅看到了移植技术的改进,从而扩大了 HCT 的治疗范围,而且还出现了一种全新的治疗策略,即使用修饰的免疫效应细胞,包括嵌合抗原受体 T 细胞和工程化 T 细胞受体。ASTCT 指南审查委员会认为,更新 ASTCT 关于 HCT 适应证的建议,纳入新数据,并酌情纳入免疫效应细胞治疗(IECT)的适应证是最佳选择。指南委员会成立了一个由移植专家、支付方代表和患者权益倡导者组成的多利益相关者工作组,为 HCT 和 IECT 的适应证提供指导。本文介绍了 ASTCT 关于 HCT 和 IECT 适应证的更新建议。HCT/IECT 的适应证分为以下几类:(1)标准治疗,适应证明确,有证据支持;(2)标准治疗,临床证据可用,虽然没有大型临床试验和观察性研究,但已证明是有效的治疗方法;(3)标准治疗,罕见适应证,用于存在明确疗效但大型临床试验和观察性研究不可行的罕见疾病;(4)发展中适应证,用于临床前和/或早期临床试验显示 HCT/IECT 是一种有前途的治疗选择的疾病;(5)不推荐,现有证据不支持常规使用 HCT/IECT。ASTCT 将继续定期审查这些指南,并在新证据出现时进行更新。

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