Results 111 to 120 of about 340,068 (318)
Alternative donor transplants for severe aplastic anemia.
Allogeneic hematopoietic stem-cell transplantation remains the only curative treatment for patients with acquired severe aplastic anemia (SAA). When a matched sibling is not available, one can search for a matched unrelated donor or a cord blood unit (CB)
A. Bacigalupo
semanticscholar +1 more source
This study demonstrates the clinical utility of a next‐generation sequencing (NGS)‐based chimerism assay (CASAL) in haematopoietic stem cell transplantation (HSCT). Compared to conventional short tandem repeat (STR) methods, CASAL showed significantly higher marker informativeness, detecting mixed chimerism (MC) below 5% recipient DNA with a median of ...
Jin Ju Kim+7 more
wiley +1 more source
Background Although the therapeutic outcome of acquired aplastic anemia has improved markedly with the introduction of immunosuppressive therapy using antithymocyte globulin and cyclosporine, a significant proportion of patients subsequently relapse and ...
Takuya Kamio+19 more
doaj +1 more source
BackgroundHaploidentical donor (HID) hematopoietic stem cell transplantation (HSCT) is an alternative treatment method for severe aplastic anemia (SAA) patients lacking suitable identical donors and those who are refractory to immunosuppressive therapy ...
Lanping Xu+12 more
semanticscholar +1 more source
This phase 2/3 study evaluated romiplostim plus ciclosporin A as first‐line treatment for patients with aplastic anaemia naïve to immunosuppressive therapy. The combination demonstrated a promising overall response rate at 27 weeks, with improvements in blood counts across multiple lineages and reduced transfusion requirements.
Jong Wook Lee+15 more
wiley +1 more source
We report an 18 year old boy with Aplastic anemia complicated by serious fungal rhinosinusitis. Despite prompt treatment and early repeated surgical debridements, he died after about more than 6 weeks of hard challenges with fungal infections.
Omid Reza Zekavat+6 more
doaj +1 more source
Circulating exosomal microRNAs in acquired aplastic anemia and myelodysplastic syndromes
Exosomal microRNAs modulate cancer cell metabolism and the immune response. Specific exosomal microRNAs have been reported to be reliable biomarkers of several solid and hematologic malignancies.
V. Giudice+11 more
semanticscholar +1 more source
Summary Paroxysmal nocturnal haemoglobinuria (PNH) is a rare, life‐threatening disorder characterized by complement‐mediated haemolysis, leading to anaemia and thrombosis. HRS‐5965 is a novel, oral, selective complement factor B inhibitor targeting the alternative pathway, potentially reducing both intra‐ and extravascular haemolysis.
Li Zhang+7 more
wiley +1 more source
Adding eltrombopag to immunosuppression: the importance of predicting outcome
André Tichelli+3 more
doaj +1 more source