CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:How I treat high-risk acute myeloid leukemia using preemptive adoptive cellular immunotherapy.
How I treat high-risk acute myeloid leukemia using preemptive adoptive cellular immunotherapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
异基因造血干细胞移植(alloHSCT)是高危急性白血病患者的一种潜在治愈性治疗手段,但不幸的是,疾病复发仍然是这些患者的主要死亡原因。供者淋巴细胞输注(DLI)有可能恢复移植物抗白血病免疫监视;然而,其疗效在不同血液系统疾病中有所差异。尽管慢性期移植后复发的慢性髓性白血病已被证明对DLI极为敏感,但复发的急性髓系白血病和急性淋巴细胞白血病的缓解率则较为有限。为预防即将发生的复发,一些研究团队探索了在检测到可测量残留病(MRD)或混合嵌合状态时抢先性给予DLI。支持该策略有效性的证据虽然令人鼓舞,但仅来自少数研究,且大多为单中心回顾性、非随机研究。本文旨在(1)讨论支持该方法的现有证据,同时强调移植后由MRD触发的治疗决策所固有的一些挑战,(2)描述其他形式的缓解后细胞治疗,包括下一代靶向特异性免疫治疗的作用,以及(3)提供一个实用框架,以支持临床医生在考虑对这一难以治疗的患者群体采用抢先性细胞治疗时的决策过程。
Allogeneic hematopoietic stem cell transplantation (alloHSCT) is a potentially curative treatment for patients with high-risk acute leukemias, but unfortunately disease recurrence remains the major cause of death in these patients. Infusion of donor lymphocytes (DLI) has the potential to restore graft-versus-leukemia immunologic surveillance; however, efficacy varies across different hematologic entities. Although relapsed chronic myeloid leukemia, transplanted in chronic phase, has proven remarkably susceptible to DLI, response rates are more modest for relapsed acute myeloid leukemia and acute lymphoblastic leukemia. To prevent impending relapse, a number of groups have explored administering DLI preemptively on detection of measurable residual disease (MRD) or mixed chimerism.
Evidence for the effectiveness of this strategy, although encouraging, comes from only a few, mostly single-center retrospective, nonrandomized studies.
This article seeks to (1) discuss the available evidence supporting this approach while highlighting some of the inherent challenges of MRD-triggered treatment decisions post-transplant, (2) portray other forms of postremission cellular therapies, including the role of next-generation target-specific immunotherapies, and (3) provide a practical framework to support clinicians in their decision-making process when considering preemptive cellular therapy for this difficult-to-treat patient population.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。