Mohammad Rafiee - Dept. of Medical Laboratory Sciences, School of Paramedical Sciences, Zanjan University of Medical Sciences, Zanjan, Iran
Hossein Bonakchi - Dept. of Biostatistics, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Sajjad Rahimi Pordanjani - Dept. of Epidemiology and Biostatistics, Semnan University of Medical Sciences, Semnan, Iran
Seyedeh Zahra Shahrokhi - Dept. of Biochemistry, School of Medicine, AJA University of Medical Sciences, Tehran, Iran
Sina Mohagheghi - Dept. of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
Mehdi Allahbakhshian Farsani - Dept. of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Mohammad Hossein Mohammadi - Dept. of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Background and Objective: Insufficient mobilization of hematopoietic stem cells and delayed engraftment are reported in autologous hematopoietic stem cell transplantation (AHSCT). The aim if this study was to identify and introduce predictive factors for mobilization and engraftment. Materials and Methods: The participants include AHSCT candidates. Pre-apheresis CD۳۴+ cells and CD۳۴+ count per kilogram (CD۳۴+ CPK) in the apheresis products were assessed by flow cytometry. There were other parameters connected to platelet and neutrophil engraftment as well as mobilization by granulocyte-stimulating growth factor (G-CSF). Univariate, multivariate, and receiver operating characteristic (ROC) analyses were used in the statistical study. Results: The predictive value of CD۳۴+ CPK for platelet engraftment was fair (AUC: ۷۶.۹%) with the cut-off of ۳.۵×۱۰۶, while it was poor for neutrophil engraftment (AUC: ۶۴.۴%) with the cut-off of ۳.۴×۱۰۶. The multiple-variate analysis demonstrated that age and CD۳۴+ CPK were positively correlated with platelet engraftment (p-values less than ۰.۰۱ and ۰.۰۰۵, respectively), while CD۳۴+ CPK and total dose of infused G-CSF (TDIG) were associated with neutrophil engraftment (p-values: ۰.۰۳). In high rates, the TDIG correlated negatively with CD۳۴+ CPK, CD۳۴+ cell counts in pre-apheresis peripheral blood samples, and total engraftment, indicating negative effects of high and long-term doses of G-CSF on mobilization and engraftment. Conclusion: The management of AHSCT will be more efficient by considering the age, CD۳۴+ CPK, and TDIG. For enhanced engraftment, adjusting the G-CSF injection days for <۴ days and total dose of G-CSF on <۴۰۰۰ micrograms are suggested.

Engraftment, Granulocyte Colony-stimulating Factor, Hematopoietic Stem Cell Transplantation, Mobilization