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降低强度预处理异基因造血干细胞移植治疗急性淋巴细胞白血病:当前证据及未来改善预后的策略。

Reduced Intensity Conditioning Allogeneic Hematopoietic Stem Cell Transplantation for Acute Lymphoblastic Leukemia; Current Evidence, and Improving Outcomes Going Forward.

机构信息

Center for Hematologic Malignancies, Knight Cancer Institute, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Mail Code L586, Portland, OR, 97239, USA.

出版信息

Curr Hematol Malig Rep. 2018 Aug;13(4):329-340. doi: 10.1007/s11899-018-0462-x.

Abstract

PURPOSE OF REVIEW

Outcomes for older adults with acute lymphoblastic leukemia (ALL) remain poor, and allogeneic hematopoietic stem cell transplant (HSCT) remains a potentially curative modality. However, benefits are offset by high rates of non-relapse mortality (NRM) in patients undergoing myeloablative conditioning (MAC) regimens. Reduced intensity conditioning (RIC) regimens can extend this therapy to adults who are unfit for MAC, although at the cost of higher relapse rates. In this review, we discuss evidence to support the usage of RIC regimens, controversies, and potential strategies to improve transplant outcomes going forward.

RECENT FINDINGS

Several novel therapies have recently been approved for the treatment of relapsed ALL and may play an important role in bridging adults with residual disease to RIC transplant. Assessing response to initial therapy via minimal residual disease (MRD) monitoring may determine which patients will derive the most benefit from allogeneic HSCT. Reduced intensity allogeneic HSCT remains a potentially curative therapy that can be offered to older adults however challenges remain. Going forward, MRD testing and novel therapies may help better select which patients should proceed to transplant and assist in getting those patients to transplant with optimally controlled disease.

摘要

目的综述

老年急性淋巴细胞白血病(ALL)患者的预后仍然较差,异基因造血干细胞移植(HSCT)仍然是一种潜在的治愈方法。然而,在接受清髓性预处理方案(MAC)的患者中,非复发死亡率(NRM)率较高,这使得该疗法的获益受到了影响。降低强度预处理方案(RIC)可以将该治疗方法扩展到不适合 MAC 的成年人,但这是以更高的复发率为代价的。在这篇综述中,我们讨论了支持使用 RIC 方案的证据、争议以及未来提高移植结果的潜在策略。

最近的发现

最近有几种新的疗法被批准用于治疗复发的 ALL,并且可能在将有残留疾病的成年人桥接到 RIC 移植方面发挥重要作用。通过微小残留病(MRD)监测评估初始治疗的反应,可能可以确定哪些患者将从异基因 HSCT 中获益最大。降低强度的异基因 HSCT 仍然是一种潜在的治愈性治疗方法,可以提供给老年患者,但仍然存在挑战。未来,MRD 检测和新疗法可能有助于更好地选择哪些患者应该进行移植,并帮助那些患者在疾病得到最佳控制的情况下进行移植。

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