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急性髓系白血病移植后维持治疗的新机制

Novel Mechanisms for Post-Transplant Maintenance Therapy in Acute Myeloid Leukemia.

作者信息

Manobianco Steven A, Rakiewicz Tara, Wilde Lindsay, Palmisiano Neil D

机构信息

Thomas Jefferson University Hospital, Jefferson University Hospitals, Philadelphia, PA, United States.

Department of Medical Oncology, Division of Hematologic Malignancy and Stem Cell Transplantation, Philadelphia, PA, United States.

出版信息

Front Oncol. 2022 Jul 12;12:892289. doi: 10.3389/fonc.2022.892289. eCollection 2022.

Abstract

Allogeneic stem cell transplantation has improved survival for patients with acute myeloid leukemia (AML), especially for patients with disease at high risk of relapse. However, relapse remains the most common cause of treatment failure and death in the post-transplant period. Maintenance therapy, an extended course of treatment after achieving remission to reduce the rate of relapse, is an important component of the treatment of various hematologic malignancies; however, its role in the treatment of AML is far less well-defined. Recently, there has been significant interest in the use of novel therapeutic agents as maintenance therapy after allogeneic stem cell transplant, utilizing new mechanisms of treatment and more favorable toxicity profiles. In this review, we will discuss the mechanistic and clinical data for post-transplant maintenance therapies in AML. Then, we will review several emergent and current clinical trials which aim to incorporate novel agents into maintenance therapy regimens.

摘要

异基因干细胞移植改善了急性髓系白血病(AML)患者的生存率,尤其是对于复发风险高的患者。然而,复发仍然是移植后治疗失败和死亡的最常见原因。维持治疗是在达到缓解后延长疗程以降低复发率,是各种血液系统恶性肿瘤治疗的重要组成部分;然而,其在AML治疗中的作用尚远未明确。最近,人们对在异基因干细胞移植后使用新型治疗药物作为维持治疗产生了浓厚兴趣,利用新的治疗机制和更有利的毒性特征。在这篇综述中,我们将讨论AML移植后维持治疗的机制和临床数据。然后,我们将回顾几项旨在将新型药物纳入维持治疗方案的正在进行和新兴的临床试验。

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Treatment of AML Relapse After Allo-HCT.异基因造血干细胞移植后急性髓系白血病复发的治疗
Front Oncol. 2021 Dec 16;11:812207. doi: 10.3389/fonc.2021.812207. eCollection 2021.

本文引用的文献

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Maintenance Therapy in AML.急性髓系白血病的维持治疗
Front Oncol. 2021 Feb 2;10:619085. doi: 10.3389/fonc.2020.619085. eCollection 2020.

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