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Results from a multi-center, non-interventional registry study for multiple myeloma patients who received stem cell mobilization regimens with and without plerixafor
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s41409-019-0676-0.pdf | Published version | 881.19 kB | Adobe PDF | View/Open |
Title: | Results from a multi-center, non-interventional registry study for multiple myeloma patients who received stem cell mobilization regimens with and without plerixafor |
Authors: | Morris, C Chabannon, C Masszi, T Russell, N Nahi, H Kobbe, G Krejci, M Auner, H Pohlreich, D Hayden, P Basak, GW Lenhoff, S Schaap, N Van Biezen, A Knol, C Iacobelli, S Liu, Q Celanovic, M Garderet, L Kröger, N |
Item Type: | Journal Article |
Abstract: | Plerixafor plus granulocyte-colony stimulating factor (G-CSF) enhances the mobilization of haematopoietic stem cells (HSCs) for collection and subsequent autologous haematopoietic stem cell transplantation (HSCT) in patients with multiple myeloma (MM).This international, multicenter, non-interventional registry study (NCT01362972), evaluated long-term outcomes for MM patients who received plerixafor versus other mobilization regimens. The comparisons were: G-CSF+plerixafor (G-CSF+P) versus G-CSF-; G-CSF+P versus G-CSF+chemotherapy (G-CSF+C); and G-CSF+P+C versus G-CSF+C. Propensity score matching was used to balance groups. Primary outcome measures were progression free survival (PFS), overall survival (OS), and cumulative incidence of relapse (CIR) after transplantation. After propensity matching, 77 versus 41 patients in the G-CSF+P versus G-CSF cohorts, 129 versus 129 in the G-CSF+P versus G-CSF+C cohort and 117 versus 117 in the G-CSF+P+C versus G-CSF+C cohort, were matched, respectively. Propensity score matching resulted in a smaller sample size and imbalances were not completely overcome. For both PFS and OS, the upper limits of the hazard ratio 95% confidence intervals exceeded pre-specified boundaries; non-inferiority was not demonstrated. CIR rates were higher in the plerixafor cohorts. G-CSF+P remains an option for the mobilization of HSCs in poor-mobilizers with MM with no substantial differences in PFS, OS and CIR in comparison with other regimens. |
Issue Date: | Feb-2020 |
Date of Acceptance: | 15-Jul-2019 |
URI: | http://hdl.handle.net/10044/1/71932 |
DOI: | 10.1038/s41409-019-0676-0 |
ISSN: | 1476-5365 |
Publisher: | Springer Nature [academic journals on nature.com] |
Start Page: | 356 |
End Page: | 366 |
Journal / Book Title: | Bone Marrow Transplantation |
Volume: | 55 |
Copyright Statement: | © The Author(s) 2019. This article is published with open access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons. org/licenses/by/4.0/ |
Keywords: | Science & Technology Life Sciences & Biomedicine Biophysics Oncology Hematology Immunology Transplantation COLONY-STIMULATING FACTOR AMERICAN SOCIETY POOR MOBILIZATION RISK-FACTORS BLOOD TRANSPLANTATION GUIDELINES OUTCOMES CHEMOTHERAPY COLLECTION 1103 Clinical Sciences 1112 Oncology and Carcinogenesis Immunology |
Publication Status: | Published |
Online Publication Date: | 2019-09-18 |
Appears in Collections: | Department of Immunology and Inflammation |