TY - JOUR A1 - Kim-Wanner, Soo-Zin A1 - Lee, Seo-Youn A1 - Seifried, Erhard A1 - Bönig, Halvard-Björn T1 - Donor-intrinsic variables determine mobilization efficiency: analyses from a cohort of sixty twice-mobilized stem cell donors T2 - Journal of translational medicine N2 - Background: Healthy volunteer registry donors have become the backbone of stem cell transplantation programs. While most registrants will never become actual donors, a small minority are called upon twice, most commonly for the same patient because of poor graft function. Anecdotal evidence provides no hard reasons to disallow second-time mobilized apheresis, but few centers have treated enough two-time donors for definitive conclusions. Moreover, for reasons unknown, the efficiency of G-CSF varies greatly between donations. Methods: Comparison of outcomes of first vs. second donations can formally confirm G-CSF responsiveness as intrinsically, likely genetically, determined. In our database, we identified 60 donors (1.3%) who received two cycles of G-CSF 24 days to 4 years apart and systematically compared mobilization outcomes. Results: First and second mobilization and collection proceeded without severe or unusual adverse effects. First-time mobilization efficiency was highly predictive of second-time mobilization. Neither mobilization efficiency nor time lag between donations affected the similarity of first- and second-time mobilization outcomes. Conclusions: With the caveat that only donors with an unremarkable first donation were cleared for a second, our data indicate that a second donation is feasible, equally tolerable as a first donation, and efficient. Moreover, the data strongly support the notion of donor-intrinsic variables dictating mobilization response and argue against relevant damage to the stem cell compartment during mobilization with rhG-CSF. KW - G-CSF KW - Mobilization KW - Stem cell KW - Allogeneic KW - Volunteer donor KW - CD34 + cells KW - Second donation Y1 - 2020 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/79267 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-792674 SN - 1479-5876 N1 - The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. N1 - Open Access funding enabled and organized by Projekt DEAL. N1 - Correspondence: h.boenig@blutspende.de; hbonig@uw.edu VL - 18 IS - art. 487 SP - 1 EP - 6 PB - BioMed Central CY - London ER -