← 返回

急性髓系白血病治疗新视角:迈向患者量身定制策略

英文原题:New Perspectives in Treating Acute Myeloid Leukemia: Driving towards a Patient-Tailored Strategy.

查看英文原题

New Perspectives in Treating Acute Myeloid Leukemia: Driving towards a Patient-Tailored Strategy.

PubMed 2022/03/31(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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。

中文摘要

数十年来,强化化疗(IC)一直被视为急性髓系白血病(AML)的最佳治疗选择,而不适合接受IC或IC治疗失败患者缺乏治愈性方案。近几年,多种新药丰富了适合及不适合接受强化治疗患者的AML治疗手段,带来新机会,也带来新挑战。这些药物包括已获批的维奈克拉、IDH1/2抑制剂恩西地平和艾伏尼布、吉妥珠单抗奥唑米星、脂质体柔红霉素/阿糖胞苷制剂CPX-351,以及口服阿扎胞苷。维奈克拉是一种BCL2抑制剂,与去甲基化药物(HMA)联用,显著改善了不适合强化治疗及老年患者的治疗管理,提高生活质量并延长生存。目前正在早期临床试验中探索维奈克拉与其他新旧药物的联合方案。具有不同作用机制的新药,以及此前已在其他疾病领域研究的新技术(如双特异性T细胞衔接器BiTE和CAR-T 细胞),也正在AML中开展探索;在研试验将有助于确定前景较好的药物、协同作用更强的组合及更佳治疗策略。应积极推动患者获得新药并参加临床试验,从而积累科学证据并确定AML未来的治疗标准。

展开英文摘要原文

For decades, intensive chemotherapy (IC) has been considered the best therapeutic option for treating acute myeloid leukemia (AML), with no curative option available for patients who are not eligible for IC or who have had failed IC. Over the last few years, several new drugs have enriched the therapeutic arsenal of AML treatment for both fit and unfit patients, raising new opportunities but also new challenges. These include the already approved venetoclax, the IDH1/2 inhibitors enasidenib and ivosidenib, gemtuzumab ozogamicin, the liposomal daunorubicin/cytarabine formulation CPX-351, and oral azacitidine.

Venetoclax, an anti BCL2-inhibitor, in combination with hypomethylating agents (HMAs), has markedly improved the management of unfit and elderly patients from the perspective of improved quality of life and better survival. Venetoclax is currently under investigation in combination with other old and new drugs in early phase trials.

Recently developed drugs with different mechanisms of action and new technologies that have already been investigated in other settings (BiTE and CAR-T cells) are currently being explored in AML, and ongoing trials should determine promising agents, more synergic combinations, and better treatment strategies. Access to new drugs and inclusion in clinical trials should be strongly encouraged to provide scientific evidence and to define the future standard of treatment in AML.

论文信息

作者
Andreozzi F、Massaro F、Wittnebel S、Spilleboudt C、Lewalle P、Salaroli A
单位
Hematology Department, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Bruxelles, Belgium.Belgium
文献类型
综述
期刊
International journal of molecular sciences2022 Mar 31
原文标识
PubMed 35409248 · DOI 10.3390/ijms23073887