Comparison of stem cell mobilization methods in multiple myeloma.

Shimazu, Yutaka; Tsukada, Nobuhiro; Maruta, Masaki; Mimura, Naoya; Takahashi, Hiroyuki; Kako, Shinichi; Kanda, Yoshinobu; Miwa, Akiyoshi et al. · Cytotherapy · 2026

retrospective_cohort · Level III

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Abstract

The advent of novel therapeutic agents has improved the prognosis of multiple myeloma (MM). However, autologous stem cell transplantation (ASCT) remains a key treatment option for eligible patients. While stem cell mobilization using cyclophosphamide and granulocyte colony-stimulating factor (G-CSF) has long been the standard approach, the introduction of plerixafor (PLER) has led to broader adoption of G-CSF±PLER-based mobilization, offering improved scheduling flexibility. Nevertheless, real-world data on current mobilization practices and their effects on post-ASCT outcomes remain limited. We evaluated mobilization strategies and their associations with clinical outcomes in MM patients who underwent ASCT between 2019 and 2022. A total of 3,319 patients were analyzed, including 743 patients mobilized with cyclophosphamide and 2,576 mobilized with G-CSF±PLER. The primary endpoint was 2-year overall survival (OS). Multivariate analysis and propensity score matching were performed to identify factors associated with superior OS. The 2-year OS rates were 89.7% (95% CI: 87.0-91.8) and 93.2% (95% CI: 91.8-94.3) in the cyclophosphamide and G-CSF groups, respectively. Multivariate analysis showed that age <65 years (P < 0.001), lower ISS stage (P < 0.001), good performance status (P < 0.001), G-CSF mobilization (P = 0.005), and deep response pre-ASCT (P < 0.001) were independent predictors of superior OS. Propensity score matching analysis demonstrated significantly better OS in the G-CSF group than in the cyclophosphamide group (P = 0.041). Among patients achieving complete or very good partial response (CR/VGPR) pre-ASCT, OS did not differ between the groups; however, among patients who did not reach CR or VGPR pre-ASCT, the G-CSF group showed significantly better OS than the cyclophosphamide group. G-CSF‒based mobilization may offer prognostic advantages after ASCT, particularly in patients with suboptimal pre-ASCT response.

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