Outcomes of melphalan 140 mg/m2 followed by autologous stem cell transplantation in multiple myeloma patients with co-morbidities: Single-centre experience

EJHaem Pub Date : 2024-08-19 DOI:10.1002/jha2.977
Dario Melotti, Samir Asher, Ethan Troy-Barnes, George Nesr, William Wilson, Marquita Camilleri, Rakesh Popat, Ke Xu, Neil Rabin, Jonathan Sive, Xenofon Papanikolaou, Lydia Lee, Annabel McMillan, Kwee Yong, Chara Kyriakou
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Abstract

High-dose melphalan followed by stem cell rescue is the standard consolidative therapy for transplant-eligible patients with multiple myeloma (MM) in the United Kingdom. A melphalan dose of 200 mg/m2 (Mel200) is considered the “gold standard” for autologous stem cell transplant (ASCT) conditioning for fit patients ≤70 years old; however, with a peak diagnosis incidence at 80–89 years old in the UK dose adjustments will be inevitable to limit toxicities. In this single-centre UK-based retrospective analysis, data was collected from patients with plasma cell dyscrasias who underwent a first reduced-intensity, Mel140, ASCT from 2006 to 2019, a total of 81 patients. We found that the procedure was overall safe with seven (9%) of patients requiring ITU admission and a single transplant-related death within the initial autograft admission. The progression-free survival (PFS) and overall survival were comparable with those previously reported in the literature with median PFS for our cohort of 31 months. Univariate analysis of our data showed an inferior PFS for patients aged ≥70 years. In conclusion, although this is a retrospective analysis, it demonstrates that dose-reduced melphalan conditioning is safe and effective in patients deemed unfit for standard-intensity conditioning.

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有并发症的多发性骨髓瘤患者接受美法仑 140 mg/m2 后进行自体干细胞移植的疗效:单中心经验
在英国,对符合移植条件的多发性骨髓瘤(MM)患者来说,大剂量美法仑(melphalan)后进行干细胞挽救是标准的巩固治疗方法。美法仑剂量为200毫克/平方米(Mel200),被认为是70岁以下适合自体干细胞移植(ASCT)的 "黄金标准";然而,在英国,80-89岁是诊断的高峰期,为限制毒性,剂量调整在所难免。在这项基于英国单中心的回顾性分析中,我们收集了2006年至2019年期间首次接受强度降低的Mel140 ASCT的浆细胞异常患者的数据,共有81名患者。我们发现,该手术总体上是安全的,有7名患者(9%)需要入住ITU,在首次自体移植入院期间有一例移植相关死亡。无进展生存期(PFS)和总生存期与之前的文献报道相当,我们队列的中位无进展生存期为 31 个月。对我们的数据进行的单变量分析表明,年龄≥70 岁的患者的无进展生存期较短。总之,尽管这是一项回顾性分析,但它表明,对于不适合接受标准强度调理的患者,剂量减低的美法仑调理是安全有效的。
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