Durgut, HimmetGürsoy, Vildan2024-11-282024-11-282022-06-110733-2459https://doi.org/10.1002/jca.21995https://hdl.handle.net/11452/48604Background Turkish Stem Cell Coordination Center (TURKOK) carries out the procurement process of unrelated allogeneic hematopoietic stem cells in Turkey. This study aims to compare the efficacy of both once-daily and divided-dose G-CSF administration and the original and biosimilar G-CSF use and the frequency and severity of adverse events in TURKOK donors. Method The study was conducted retrospectively with 142 healthy TURKOK donors. For PBSC mobilization, two different subcutaneous G-CSF programs were used as 10 mu/kg/day single-dose and 5 mu/kg/12 h. Neupogen (Amgen, Puerto Rico) and Tevagrastim (Teva, Kfar Saba, Israel) were used as G-CSF. All donors started apheresis on the fifth day, and all side effects were recorded during the procedure. Results Stem cell yield was similar between single-dose and divided-doses based on donor weight, favoring the split-dose based on recipient weight (P = .506 and P = .023, respectively). Both G-CSF posologies were comparable if the target CD34+ cell yield was >= 4 x 10(6)/kg. CD34+ cell yield was equivalent when evaluated against recipient weight, significantly favoring Tevagrastim vs Neupogen by donor weight (P = .740 and P = .021, respectively). Side effects, duration of pain, and need for analgesia favor Tevagratim over Neupogen. Conclusion Split-dose may be recommended for cases where the need for large numbers of CD34+ cells to be harvested is anticipated due to significant cell yield relative to recipient weight. However, sufficient hematopoietic stem cells can be collected with both posology. Tevagrastim is non-inferiority effective to Neupogen. Side effects during administration are both low-grade and temporary.eninfo:eu-repo/semantics/closedAccessHealthy donorsMobilizationBloodFilgrastimTransplantationEventsCancerSafetyBiosimilar g-csfFilgrastimSingle-doseSplit-doseUnrelated hematopoietic stem cell donorsScience & technologyLife sciences & biomedicineHematologyArticle00080942120000143043737510.1002/jca.21995