AI Article Synopsis

  • Nivestym, a biosimilar to Neupogen, is being evaluated for its effectiveness in mobilizing peripheral blood stem cells (PBSC) in healthy donors for allogeneic hematopoietic stem cell transplantation (allo-HSCT).
  • A retrospective study analyzed data from 541 donors who received either Nivestym or Neupogen, focusing on factors like donor age, weight, and various counts of cells before and after treatment.
  • Results showed that while Nivestym was generally as effective as Neupogen for PBSC mobilization, younger donors (under 35) had a slightly lower CD34 cell count after using Nivestym compared to those using Neupogen.

Article Abstract

Background: Nivestym, a biosimilar granulocyte colony-stimulating factor (G-CSF) to the originator filgrastim (Neupogen), is now being used for the mobilization of peripheral blood stem cells (PBSC) in allogeneic hematopoietic stem cell transplantation (allo-HSCT). We aim to compare the efficacy of Nivestym and Neupogen for PBSC mobilization in healthy allogeneic donors.

Methods: We conducted a retrospective single-center study including 541 adult allo-HSCT donors receiving Nivestym (January 2013-July 2020), or Neupogen (July 2020-June 2023) for donor PBSC mobilization. Bivariate analysis was conducted using SPSS version 28. Statistical significance was determined at a p-value <.05.

Results: Our study included 541 allo-HSCT donors who received Neupogen (n = 345, 64%) or Nivestym (n = 196, 36%) for PBSC mobilization. The median age was 47 years (range 17-76). The median donor weight was 86 kg (95% confidence interval [CI]: 87-91). Donors receiving Neupogen had similar pre-G-CSF white blood cell count, CD34 percentages, and circulating CD34 count compared with donors receiving Nivestym. The Neupogen group had similar median PBSC product total neutrophil count, CD34 percentage, absolute CD34 count, and infused CD34 dose compared with the Nivestym group. For donors aged 35 years or younger, the median CD34 dose was higher in donors who received Neupogen compared with Nivestym (6.9 vs. 6.3 million cells/kg, p = .044).

Conclusions: Nivestym demonstrated similar efficacy for PBSC mobilization compared with Neupogen among allo-HSCT donors. In donors aged 35 years or younger, a slightly lower PBSC product CD34 count was noted with Nivestym compared with Neupogen.

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Source
http://dx.doi.org/10.1111/trf.17909DOI Listing

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