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Relapse and graft-versus-host disease (GVHD) are currently the predominant causes of mortality post allogeneic hematopoietic stem cell transplantation (allo-HSCT). The contentious use of antithymocyte globulin (ATG) for preventing GVHD in matched sibling HSCT scenarios has been a topic of significant debate. A retrospective analysis was conducted on matched sibling HSCT cases with high-risk factors for GVHD in our center from January 2018 to June 2023. Our assessment revealed that the group administered with ATG exhibited a 30 % incidence of acute GVHD (aGVHD), in contrast to 81.8 % in the non-ATG cohort (P = 0.037) among matched sibling HSCT cases with high GVHD risk factors. Furthermore, chronic GVHD (cGVHD) occurred in 20 % of the ATG group and 72.7 % of the non-ATG group (P = 0.03). Notably, the administration of ATG did not significantly impact disease relapse (p = 0.149), infection rates (p = 0.64), granulocyte recovery time (p = 0.15), platelet recovery time (p = 0.12), overall survival (p = 0.889), or disease-free survival time (p = 0.787). The use of rabbit antithymocyte globulin (r-ATG) at a 5 mg/kg dosage demonstrated a notable reduction in aGVHD and cGVHD incidences within sibling matched HSCT cases with high-risk factors for GVHD, without increasing rates of disease recurrence or infections. These findings highlight the potential benefit of using low-dose r-ATG in high-risk of GVHD sibling matched allogeneic HSCTs, although further validation with a larger cohort is necessary.
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http://dx.doi.org/10.1016/j.trim.2024.102131 | DOI Listing |
Hematology
December 2025
The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
The present study aimed to compare the efficacy and safety of hematopoietic stem cell transplantation (HSCT) and immunosuppressive therapy (IST) for hepatitis-associated aplastic anemia (HAAA). Studies comparing HSCT with IST in HAAA were retrieved from inception to July 22, 2024, including 12 studies with a total of 544 cases for meta-analysis. Meta-analysis demonstrated significantly superior outcomes in the HSCT group versus IST, which was manifested as lower overall mortality ( < 0.
View Article and Find Full Text PDFCureus
July 2025
Department of Mother and Child, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, ROU.
Introduction: Hemophagocytic lymphohistiocytosis (HLH) is a disease characterized by systemic hyperinflammation, a so-called cytokine storm that leads to life-threatening complications. Up to this date, there is only one protocol available for patients with this pathology, and there are no second-line therapy protocols in cases of relapsed or refractory diseases.
Materials And Methods: This is a retrospective observational study of patients treated in the Department of Pediatric Hematology and Oncology, Pediatric Clinic No.
Braz J Med Biol Res
August 2025
The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
This study aimed to systematically evaluate the risk of drug-induced pulmonary edema (DIPE) using the Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) database. This retrospective pharmacovigilance study utilized FAERS data from the first quarter of 2004 to the second quarter of 2024. We identified drugs with at least 10 reported DIPE cases as primary suspects (PS).
View Article and Find Full Text PDFHaematologica
August 2025
Department of Hematology and Bone Marrow Transplantation, Saint-Louis Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France; INSERM U1342, Saint Louis Research Institute, IHU Leukemia Institute Paris Saint Louis, SIRIC InSitu, Paris Cité University, Paris.
Allogeneic hematopoietic stem cell transplantation (alloHSCT) from mismatched unrelated donors (MMUD) carries high risks of non-relapse mortality (NRM) and graft-versus-host disease (GVHD). Post-transplant cyclophosphamide (PTCY) has emerged as an alternative to antithymocyte globulin (ATG) for GVHD prophylaxis. This single-center retrospective study compared PTCY (n=41) to high-dose ATG and low-dose ATG in 155 MMUD alloHSCT recipients.
View Article and Find Full Text PDFCureus
August 2025
Nephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, IND.
Background ABO-incompatible kidney transplantation (ABOi KT) expands access to living-donor organs but requires careful control of pre-existing anti-ABO isoagglutinins to minimize antibody-mediated rejection (ABMR). The present study was designed with the following objectives: The primary objective was to assess the relationship between baseline anti-ABO IgG titers (≥ 64 vs. < 64) and the intensity of therapeutic plasma exchange (TPE) required pre- and post-transplant, as well as ABMR incidence.
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