Efficacy and safety profile of busulfan plus low-dose melphalan (BUMEL) versus high-dose melphalan (MEL200) as a conditioning regimen for autologous hematopoietic stem cell transplantation (auto-HSCT) in multiple myeloma patients: a systematic review and meta-analysis.

IF 2.8 4区 医学 Q2 HEMATOLOGY
Expert Review of Hematology Pub Date : 2026-06-01 Epub Date: 2026-03-24 DOI:10.1080/17474086.2026.2649831
Shahzaib Maqbool, Imran Khan, Muhammad Ibrahim, Aye Mon Thida, Muhamamd Salman Faisal, Fatima Faraz, Abat Khan, Moazzam Shahzad, Mohammad Ebad Ur Rehman, Qurat Ul Ain Muhammad, Abdur Rehman
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引用次数: 0

Abstract

Introduction: The optimal conditioning regimen prior to autologous stem cell transplantation (Auto-HSCT) in multiple myeloma remains uncertain. We conducted a systematic review and meta-analysis to compare the efficacy and safety of busulfan-melphalan (BUMEL) versus high-dose melphalan (HDMEL) conditioning.

Methods: A systematic literature search of PubMed, Embase, and the Cochrane Library was performed to from inception to 15 April 2025 to identify comparative studies evaluating BUMEL and HDMEL conditioning prior to Auto-HSCT. Eligible studies reported efficacy and/or safety outcomes. Risk of bias was assessed using standard methodological criteria. Pooled hazard ratios and odds ratios with 95% confidence intervals were calculated using random-effects models.

Results: Eleven studies comprising transplant-eligible patients with multiple myeloma were included. BUMEL conditioning was associated with improved progression-free survival compared with HDMEL, favoring BUMEL (HR: 0.83, 95% CI: 0.76-0.89, p < 0.00001), while no definitive overall survival benefit was observed HR: 1.10, 95% CI: 1.00-1.21, p = 0.05). BUMEL was associated with higher rates of mucositis, infections, and hepatic toxicity.

Conclusions: BUMEL conditioning offers improved disease control at the cost of increased toxicity, without a clear overall survival advantage. These findings support individualized conditioning selection, particularly in settings where upfront ASCT remains standard practice.

Registration: This protocol was registered on PROSPERO with an ID of CRD420261292372.

busulfan +低剂量melphalan (BUMEL)与高剂量melphalan (MEL200)作为多发性骨髓瘤患者自体造血干细胞移植(auto-HSCT)的调节方案的疗效和安全性:一项系统回顾和荟萃分析。
自体干细胞移植(Auto-HSCT)治疗多发性骨髓瘤前的最佳调理方案仍不确定。我们进行了一项系统回顾和荟萃分析,比较了busulfan - melphalan (BUMEL)与高剂量melphalan (HDMEL)的疗效和安全性。方法:系统检索PubMed, Embase和Cochrane图书馆的文献,从创建到2025年4月15日,以确定在Auto-HSCT之前评估BUMEL和HDMEL条件反射的比较研究。符合条件的研究报告了疗效和/或安全性结果。采用标准方法学标准评估偏倚风险。采用随机效应模型计算95%置信区间的合并风险比和优势比。结果:11项研究纳入了符合移植条件的多发性骨髓瘤患者。与HDMEL相比,BUMEL调节与改善的无进展生存相关,BUMEL更有利(HR: 0.83, 95% CI: 0.76-0.89, p p = 0.05)。BUMEL与较高的黏膜炎、感染和肝毒性发生率相关。结论:BUMEL调节以增加毒性为代价改善了疾病控制,没有明显的总体生存优势。这些发现支持个性化条件选择,特别是在预先ASCT仍然是标准做法的情况下。该协议在PROSPERO上注册,ID为CRD420261292372。
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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