成人复发或难治性急性淋巴细胞白血病(ALL)的不良事件:近期临床试验的文献综述

H. Hummel, M. Topp, E. Chang, V. Chia, M. Kelsh, Martha L Doeml, S. Alekar, A. Stein
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引用次数: 5

摘要

背景:随着复发或难治性(R/R)急性淋巴细胞白血病(ALL)成人患者的新治疗方案的引入,需要更好地了解现有的毒性特征。方法:系统回顾文献,总结在费城染色体阳性(Ph+)和费城染色体阴性(Ph-) R/R ALL的临床试验中使用化疗方案、基于酪氨酸激酶抑制剂(TKI)的方法或其他靶向治疗的毒性概况。17篇符合条件的文章报告了毒性概况。我们将不良事件分为以下几类:血液学、感染性、胃肠道、心血管/肾脏/肝脏和神经学,并按治疗类型分层。还总结了治疗相关或早期/诱发死亡率。结果:在细胞毒性化疗及其联合化疗中,血液学不良事件最常见,几乎影响所有患者,其次是感染,大多数患者报告感染。神经毒性是与长春新碱脂质体相关的最常见不良事件。与化疗相比,基于tki的治疗显示出明显的安全性。尽管血液学不良事件仍然是最常见的毒性,但基于tki的治疗的感染发生率(9-18%)低于化疗(56-100%)。恶心、呕吐和腹泻是接受TKIs后主要的胃肠道不良事件,而粘膜炎似乎更具有细胞毒性化疗的特征。结论:本文系统回顾了目前标准化疗对R/R Ph-或Ph+ ALL成人患者的安全性。总的来说,不良事件的记录在研究中是高度可变的,排除了直接比较或汇总结果。然而,这项系统的文献综述首次总结和量化了主要化疗和基于tki的方案对成年R/R ALL患者的毒性概况,为与新兴疗法的比较提供了基线。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adverse Events in Adults with Relapsed or Refractory Acute Lymphoblastic Leukemia (ALL): A Literature Review of Recent Clinical Trials
Background: With the introduction of new therapy options for adult patients with relapsed or refractory (R/R) acute lymphoblastic leukemia (ALL), a better understanding of existing toxicity profiles is needed. Methods: A systematic literature review was conducted to summarize the toxicity profiles in clinical trials using chemotherapeutic regimens, tyrosine kinase inhibitor (TKI)-based approaches in Philadelphia chromosome-positive (Ph+) and Philadelphia chromosome-negative (Ph-) R/R ALL, or other targeted therapies. Seventeen eligible articles were identified that reported toxicity profiles. We grouped adverse events into the following categories: hematological, infectious, gastrointestinal, cardiovascular/renal/hepatic, and neurological, stratified by treatment type. Treatment-related or early/induction mortality was also summarized. Results: With cytotoxic chemotherapy and its combinations, hematological adverse events were the most common, affecting virtually all patients, followed by infections, which were reported in most patients. Neurologic toxicity was the most common adverse event associated with liposomal vincristine. TKI-based treatments showed a distinct safety profile compared with the chemotherapies. Although hematological adverse events still represented the most common toxicity, infections were less common with TKI-based therapies (9-18%) than with chemotherapies (56-100%). Nausea, vomiting, and diarrhea were the predominant gastrointestinal adverse events after receipt of TKIs, whereas mucositis appeared to be more characteristic of cytotoxic chemotherapy. Conclusions: This paper provides a systematic review of the safety profile of current standard chemotherapy for adults with R/R Ph- or Ph+ ALL. Overall, documentation of adverse events was highly variable across the studies, precluding direct comparisons or pooling of results. However, this systematic literature review is the first to summarize and quantify the toxicity profiles of mainly chemotherapeutic and TKI-based regimens for adult patients with R/R ALL, providing a baseline for comparison with emerging therapies.
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