Haploidentical hemopoietic cell transplantation (haplo-SCT) is a therapeutic option in patients with acquired severe aplastic anemia (SAA); failure of one course of immune suppressive therapy (IST) with antithymocyte globulin (ATG) and the lack of an HLA-matched related or unrelated donor are accepted criteria for considering haplo-SCT treatment. Prevention of graft-versus-host disease (GvHD) in haplo-SCT is provided both by ex vivo T-cell depletion and by extensive drug GvHD prophylaxis after unmanipulated graft. Haploidentical transplant for IST-refractory SAA is a clinical option offered in centers with established experience in haplo-SCT and should be applied within clinical protocol aimed at maximally preventing graft rejection and GvHD.

Haploidentical Transplantation

Ciceri F.
Primo
;
2017-01-01

Abstract

Haploidentical hemopoietic cell transplantation (haplo-SCT) is a therapeutic option in patients with acquired severe aplastic anemia (SAA); failure of one course of immune suppressive therapy (IST) with antithymocyte globulin (ATG) and the lack of an HLA-matched related or unrelated donor are accepted criteria for considering haplo-SCT treatment. Prevention of graft-versus-host disease (GvHD) in haplo-SCT is provided both by ex vivo T-cell depletion and by extensive drug GvHD prophylaxis after unmanipulated graft. Haploidentical transplant for IST-refractory SAA is a clinical option offered in centers with established experience in haplo-SCT and should be applied within clinical protocol aimed at maximally preventing graft rejection and GvHD.
2017
Inglese
Congenital and Acquired Bone Marrow Failure
9780128041758
Elsevier Inc.
121
125
5
https://www.sciencedirect.com/science/article/pii/B9780128041529000105?via=ihub
Sì, ma tipo non specificato
Internazionale
Goal 3: Good health and well-being
Aplastic anemia
Haploidentical
Transplantation
No
2 Contributo in Volume::2.1 Contributo in volume (Capitolo o Saggio)
2
268
none
Ciceri, F.; Stanghellini, M. T. L.
info:eu-repo/semantics/bookPart
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/138419
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