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Non-cryopreserved hematopoietic stem cell transplantation compared to conventional autologous peripheral stem cell transplantation with cryopreserved stem cells among patients newly diagnosed with myeloma

dc.contributor.authorVural, Ece
dc.contributor.authorOcal, Ramazan
dc.contributor.authorAytekin, Hamit
dc.contributor.authorAksoyoglu, Ilknur
dc.contributor.authorNevruz, Oral
dc.contributor.authorIlhan, Osman
dc.contributor.authorBeksac, Meral
dc.date.accessioned2026-10-09T21:48:29Z
dc.date.issued2026
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstractHematopoietic stem cells are traditionally cryopreserved (CP) until transfusion. Melphalan's half-life is 75 min and allows transplantation of fresh non-CP hematopoietic stem cells (HSCs). There are a few studies in lymphoma and myeloma focusing on the role of autologous stem cell transplantation (ASCT) with fresh HSCs. In this single-center study, we aimed to compare the engraftment kinetics of non-CP versus conventional ASCT. Of 125 transplants performed among 121 myeloma patients, 44 were with conventional CP, while 81 were using non-CP products. Four patients with high-risk myeloma received tandem ASCT with non-CP followed by CP products. Non-CP patients compared to CP received similar induction regimens but more frequent Plerixafor (50.6% vs. 19%, p < 0.001) resulting in higher CD34 cell mobilization and transfusion (8.32 vs. 5.2 & times;10(6)/kg, p < 0.001). Neutrophil and platelet engraftments between CP vs. non-CP groups were 11 (9-17) vs. 11.5 (10-19) days (p < 0.001) and 11 days (p = 0.31) in both, respectively. Complications such as mucositis and diarrhea of all grades were similar, but infusion-related reactions (15.9% vs 2.5%, p = 0.009) were more frequent with longer hospital stays (15 vs 14 days, p = 0.019) among CP compared to non-CP ASCTs. In conclusion, a statistically significant but clinically not meaningful faster neutrophil engraftment, fewer infusion-related reactions, and one day shorter duration of hospitalization were observed, all in favor of non-CP products, which also happens to coincide with more frequent use of plerixafor in our experience.
dc.identifier.doi10.1016/j.transci.2026.104493
dc.identifier.issn1473-0502
dc.identifier.issn1878-1683
dc.identifier.issue4
dc.identifier.orcid0000-0002-2754-8995
dc.identifier.orcid0009-0005-7849-3057
dc.identifier.pmid42462602
dc.identifier.scopus2-s2.0-105044657783
dc.identifier.scopusqualityQ3
dc.identifier.urihttps://doi.org/10.1016/j.transci.2026.104493
dc.identifier.urihttps://hdl.handle.net/20.500.12794/3575
dc.identifier.volume65
dc.identifier.wosWOS:001827279600001
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynak.digerScience Citation Index Expanded (SCI-EXPANDED)
dc.language.isoen
dc.publisherPergamon-Elsevier Science Ltd
dc.relation.ispartofTransfusion and Apheresis Science
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.sdgGoal-03: Good Health and Well-Being
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260922
dc.subjectMultiple Myeloma
dc.subjectAutologous
dc.subjectNon-Cryopreserved
dc.subjectPeripheral Blood Stem Cell
dc.titleNon-cryopreserved hematopoietic stem cell transplantation compared to conventional autologous peripheral stem cell transplantation with cryopreserved stem cells among patients newly diagnosed with myeloma
dc.typeArticle

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