Is intensive chemotherapy and allogeneic stem cell transplantation mandatory for curing Philadelphia chromosome-positive acute lymphoblastic leukemia in young patients in the era of multitarget agents?

IF 2.3 4区 医学 Q2 HEMATOLOGY
Expert Review of Hematology Pub Date : 2024-07-01 Epub Date: 2024-05-20 DOI:10.1080/17474086.2024.2357273
Sang Kyun Sohn, Jung Min Lee, Youngeun Jang, Yunji Lee, Jihyun Na, Hee Jeong Cho, Joon Ho Moon, Dong Won Baek
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Abstract

Introduction: The treatment outcomes for Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) have improved with various tyrosine kinase inhibitors (TKIs) and bispecific T-cell engagers. Although allogeneic stem cell transplantation (allo-SCT) is the standard treatment for young patients with Ph+ALL, its role remains debatable in the era of TKIs and blinatumomab.

Areas covered: There are some issues regarding Ph+ALL. First, do young patients require intensive chemotherapy (IC) in the era of multitarget agents? Second, which TKI is preferred for frontline therapy? Third, should allo-SCT be performed in patients achieving complete remission with ponatinib and IC? Fourth, can chemo-free treatment lead to a cure without allo-SCT? We searched relevant literature from the last 30 years on PubMed; reviewed the role of chemo-free therapies and combinations of ponatinib and IC; and assessed the necessity of allo-SCT in young patients with Ph+ALL.

Expert opinion: Allo-SCT may not be needed, even in young patients with Ph+ALL treated with ponatinib-based IC or combined ponatinib and blinatumomab as frontline therapy. When adopting a ponatinib-based chemo-minimized regimen for induction, allo-SCT is needed with posttransplant ponatinib maintenance. Continuous exposure to ponatinib at pre- or post-transplant is regarded as one of the most important factor for the success of treatment.

多靶点药物时代,年轻患者是否必须接受强化化疗和异基因干细胞移植才能治愈费城染色体阳性急性淋巴细胞白血病?
简介:各种酪氨酸激酶抑制剂(TKIs)和双特异性T细胞诱导剂改善了费城染色体阳性急性淋巴细胞白血病(Ph+ALL)的治疗效果。尽管异基因干细胞移植(allo-SCT)是年轻Ph+ALL患者的标准治疗方法,但在TKIs和blinatumomab时代,其作用仍有待商榷:Ph+ALL 存在一些问题。首先,在多靶点药物时代,年轻患者是否需要强化化疗(IC)?第二,一线治疗首选哪种 TKI?第三,使用泊纳替尼和 IC 获得完全缓解的患者是否应该进行异体造血干细胞移植?第四,不进行allo-SCT的无化疗治疗能否导致治愈?我们在PubMed上检索了过去30年的相关文献,回顾了无化疗疗法和帕纳替尼与IC联合疗法的作用,并评估了在年轻的Ph+ALL患者中进行allo-SCT的必要性:即使年轻的Ph+ALL患者接受了以泊纳替尼为基础的IC或泊纳替尼与blinatumomab联合疗法作为一线疗法,也可能不需要进行allo-SCT。在采用基于泊纳替尼的化疗最小化方案进行诱导治疗时,需要在移植后维持泊纳替尼,进行异体造血干细胞移植。在移植前或移植后持续服用泊纳替尼被认为是治疗成功的最重要因素之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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