Smit Yolba, Scheuter Pien, Lange Myrthe P M, Janssen Jeroen J W M, Posthuma Eduardus F M, Bekker Charlotte L, Hermens Rosella P M G, Blijlevens Nicole M A
Department of Hematology, Radboud university medical center, Route 476, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands.
Department of Internal Medicine, Reinier de Graaf Hospital, Delft, The Netherlands.
Support Care Cancer. 2025 May 3;33(5):446. doi: 10.1007/s00520-025-09451-4.
One in five chronic myeloid leukemia (CML) patients experiences such intolerability that they switch tyrosine kinase inhibitor (TKI) treatment within 3 years. Information on tolerability is needed to guide shared decision-making. However, an overview of symptoms patients experience per TKI is lacking, and physician-graded toxicity underestimates patients' experiences.
We systematically searched PubMed and Embase from inception to February 2025 and conducted a meta-analysis on the prevalence of patient-reported symptoms in CML per TKI. This study follows the Preferred Reporting Items for Systematic Reviews (PRISMA) guideline for systematic reviews.
We included 11 studies with 2987 patients, reporting on 47 different symptoms of any severity. The low-grade patient-reported symptom burden was high. No data were available on asciminib and ponatinib, and minimal data were available for bosutinib. In indirect, unadjusted comparisons, 13 out of 47 symptoms (of any severity) showed significant differences in prevalence between common TKI types.
Our findings provide essential information to guide treatment decisions in cases of intolerability. However, there is a clear need for further research with standardized instruments, especially in second and third generation TKI types, including direct comparisons and comparisons adjusted for covariates.
五分之一的慢性髓性白血病(CML)患者会出现难以耐受的情况,以至于他们在3年内更换酪氨酸激酶抑制剂(TKI)治疗。需要有关耐受性的信息来指导共同决策。然而,目前缺乏每种TKI治疗的患者所经历症状的概述,并且医生分级的毒性低估了患者的实际体验。
我们系统地检索了从数据库建立到2025年2月的PubMed和Embase,并对每种TKI治疗的CML患者报告症状的患病率进行了荟萃分析。本研究遵循系统评价的首选报告项目(PRISMA)指南。
我们纳入了11项研究,共2987名患者,报告了47种不同严重程度的症状。患者报告的低级别症状负担较高。关于asciminib和ponatinib没有可用数据,关于bosutinib的数据极少。在间接的、未调整的比较中,47种症状(任何严重程度)中有13种在常见TKI类型之间的患病率存在显著差异。
我们的研究结果为指导不耐受情况下的治疗决策提供了重要信息。然而,显然需要使用标准化工具进行进一步研究,特别是在第二代和第三代TKI类型中,包括直接比较和针对协变量进行调整的比较。