Haplo?identical or mismatched unrelated donor hematopoietic cell transplantation for <scp>Fanconi</scp> anemia: Results from the <scp>Severe Aplastic Anemia Working Party</scp> of the <scp>EBMT</scp>
نویسندگان
چکیده
Allogeneic hematopoietic cell transplantation (HCT) is the only curative option for bone marrow failure or malignant diseases Fanconi anemia (FA) patients. Although results have improved over last decades, reaching more than 90% survival when a human leukocyte antigen (HLA)-identical donor available, alternative HCT donors are still less reported. We compared outcomes using HLA-mismatched unrelated (MMUD; n = 123) haplo-identical (HDs), either in vivo T depletion (n 33) cells depleted with some type of graft manipulation ex 59) performed FA between 2000 and 2018. Overall (OS) by 24 months was 62% (53–71%) MMUD, versus 80% (66–95%) HDs 60% (47–73%) (p .22). Event-free (EFS) better HD-transplanted patients 86% (73–99%) those transplanted from MMUD 58% (48–68%) 56% (42–69%) .046). Grade II-IV acute graft-versus-host disease (GVHD) 41% (MMUD) 40% (HDs no manipulation) 17% graft), .005). No differences were found other transplant related outcomes. These data suggest that might be considered as an EFS unmanipulated grafts.
منابع مشابه
Alternative donor transplantation for aplastic anemia.
Patients with severe aplastic anemia who do not have a human leukocyte antigen (HLA)-identical sibling generally receive immunosuppressive therapy as a first-line therapy, with allogeneic transplantation being reserved for those who do not have an adequate sustained response. Barriers to the use of unrelated-donor transplantation for aplastic anemia include identifying a suitable alternative do...
متن کاملClinical applications of haploidentical hematopoietic stem cell transplantation in severe aplastic anemia.
OBJECTIVE The purpose of this study was to investigate the efficacy and safety of haploidentical allogeneic hemopoietic stem cell transplantation (allo-HSCT) in severe aplastic anemia (SAA) and prophylaxis of complications involved. PATIENTS AND METHODS 8 patients with clinically diagnosed SAA (5 cases of SAA-I and 3 cases of SAA-II) were recruited, with the parents as the donors of hemopoiet...
متن کاملHaploidentical hematopoietic stem cell transplantation in children and adolescents with acquired severe aplastic anemia
Severe aplastic anemia (SAA) is a life-threatening disorder for which allogeneic hematopoietic stem cell transplantation (HSCT) is the current available curative treatment. HSCT from matched sibling donors (MSDs) is the preferred therapy for children with acquired SAA. For patients who lack MSDs, immunosuppressive therapy (IST) is widely accepted as a first-line treatment before considering HCT...
متن کاملAssociation between donor leukocyte telomere length and survival after unrelated allogeneic hematopoietic cell transplantation for severe aplastic anemia.
IMPORTANCE Telomeres protect chromosome ends and are markers of cellular aging and replicative capacity. OBJECTIVE To evaluate the association between recipient and donor pretransplant leukocyte telomere length with outcomes after unrelated donor allogeneic hematopoietic cell transplantation (HCT) for patients with severe aplastic anemia. DESIGN, PARTICIPANTS, AND SETTING The study included...
متن کاملEffect of stem cell source on outcomes after unrelated donor transplantation in severe aplastic anemia.
Outcome after unrelated donor bone marrow (BM) transplantation for severe aplastic anemia (SAA) has improved, with survival rates now approximately 75%. Increasing use of peripheral blood stem and progenitor cells (PBPCs) instead of BM as a graft source prompted us to compare outcomes of PBPC and BM transplantation for SAA. We studied 296 patients receiving either BM (n = 225) or PBPC (n = 71) ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 2021
ISSN: ['0361-8609', '1096-8652']
DOI: https://doi.org/10.1002/ajh.26135