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Cord blood (CB) transplantation has fallen into disfavor because of its association with low cell dose and high non-relapse mortality (NRM). However, a phase I to II trial using UM171-expanded CB transplantation in patients with high-risk hematologic malignancies who lacked a suitable donor demonstrated promising results, including prompt neutrophil engraftment, the ability to use smaller, better human leucocyte antigen (HLA)- matched CB units, and a low NRM rate of 5%. This retrospective matched paired analysis was conducted to test the hypothesis that UM171-expanded CB transplantation provides outcomes equivalent or superior to those of conventional hematopoietic stem cell donor sources. The primary objectives were neutrophil engraftment, NRM, and graft versus host disease (GVHD)-free, relapse-free survival (GRFS). This retrospective study compared the outcomes of the 22 adult patients who received a single UM171-expanded CB transplant in the phase I to II trial to those of six cohorts of patients allografted from different stem cell sources, as reported to the European Society for Blood and Marrow Transplantation (EBMT) registry. The six donor control cohorts included: (1) unmanipulated CB, (2) peripheral blood stem cells (PBSC) from a 10/10 HLA-matched unrelated donor (10/10 MUD), (3) bone marrow (BM) from a 10/10 MUD, (4) 9/10 matched unrelated donor (9/10 UD), (5) T cell replete haploidentical (haplo) donor, and (6) HLA- matched sibling donor (MSD). Direct and propensity score matching was used for patient, disease, and transplant characteristics to ensure comparability. The analyzed endpoints included engraftment, GVHD, NRM, relapse, progression-free survival (PFS), overall survival (OS), and GRFS. Neutrophil engraftment was generally similar in all donor groups but was slower for both unmanipulated CB and MUD BM. There was no moderate to severe chronic GVHD in the UM171 CB recipients, with significantly lower rates compared to PBSC MUD, BM MUD, and MSD transplants. PFS, OS, and GRFS were all significantly better with UM171 CB than those seen with haplo donor transplants. GRFS was also consistently superior with UM171 CB when compared to 10/10 MUD PBSC, 9/10 UD, and MSD transplants. UM171-expanded CB recipients have equivalent or improved short- and long-term outcomes compared to patients transplanted from other graft sources.
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http://dx.doi.org/10.1016/j.jtct.2025.08.006 | DOI Listing |
Transplant Cell Ther
September 2025
Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan; Department of Hematology and Clinical Immunology, Yokohama City University School of Medicine, Yokohama, Japan.
The Dynamic International Prognostic Scoring System for primary myelofibrosis (DIPSS) has been reported to predict transplant outcomes in myelofibrosis (MF) patients. Recently, the pre-transplant use of JAK inhibitors has become common in clinical practice, but it is unclear whether DIPSS is also useful for predicting transplant outcomes for these patients. In this study, we compared the prognostic impact of DIPSS between MF patients with and without pre-transplant Ruxolitinib therapy.
View Article and Find Full Text PDFAnn Hematol
September 2025
Hematology Unit, Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, Italy.
Daratumumab combined with bortezomib, thalidomide, and dexamethasone (Dara-VTD) is a highly effective induction therapy for newly diagnosed multiple myeloma (NDMM) patients eligible for autologous stem cell transplantation (ASCT). However, its impact on stem cell mobilization requires a critical evaluation. This study examines the effects of Dara-VTD on stem cell mobilization and collection outcomes.
View Article and Find Full Text PDFCureus
August 2025
Medical Oncology, Burjeel Medical City, Burjeel Cancer Institute, Abu Dhabi, ARE.
Introduction Allogeneic hematopoietic stem cell transplantation (HSCT) saves lives by treating a diverse range of pediatric conditions. Pediatric HSCT services began in the UAE in 2022. This study evaluates outcomes of the first 25 cases at Burjeel Medical City, Burjeel Cancer Institute, Abu Dhabi, following the establishment of the UAE's first pediatric bone marrow transplantation (BMT) unit.
View Article and Find Full Text PDFPharmaceutics
August 2025
Department of Clinical Pharmacy, School of Pharmacy, Faculty of Medicine, Hebrew University of Jerusalem, P.O.Box 12272, Jerusalem 9112102, Israel.
Busulfan is a key component of myeloablative conditioning regimens in hematopoietic stem cell transplantation (HSCT) for pediatric patients with acute myeloid leukemia, solid tumors, and certain non-malignant diseases. This study compares the clinical outcomes of once-daily (BU1) versus four-times-daily (BU4) busulfan dosing regimens in pediatric HSCT recipients. A retrospective analysis was conducted on 70 pediatric patients who underwent HSCT at Hadassah Medical Center between June 2018 and October 2023.
View Article and Find Full Text PDFCancers (Basel)
August 2025
Department of Medicine, Division of Hematology and Oncology, University at Buffalo, Buffalo, NY 14203, USA.
Mucositis involving the gastrointestinal, vaginal, and nasal mucosa is one of the primary dose-limiting toxicities of hematopoietic stem cell transplantation (HSCT) and its conditioning regimen. The oropharyngeal mucosa is commonly affected, which can be detrimental to patient health and quality of life. Despite its significant prevalence and deleterious effects, we have an inadequate understanding of the risk factors and outcomes associated with oral mucositis (OM).
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