Data di Pubblicazione:
2015
Abstract:
Hematopoietic SCT (HSCT) from HLA haploidentical family donors is a promising therapy for high-risk hematological malignancies. In the past 15 years at San Raffaele Scientific Institute, we investigated several transplant platforms and post transplant cellular-based interventions. We showed that T cell-depleted haploidentical transplantation followed by the infusion of genetically modified donor T cells (TK007 study, Eudract-2005-003587-34) promotes fast and wide immune reconstitution and GvHD control. This approach is currently tested in a phase III multicenter randomized trial (TK008 study, NCT00914628). We targeted patients with advanced leukemia with a sirolimus-based, calcineurin inhibitor-free prophylaxis of GvHD to allow the safe infusion of unmanipulated PBSCs from haploidentical family donors (TrRaMM study, Eudract 2007-5477-54). Results of these approaches are summarized and discussed.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
haploidentical HSCT
Elenco autori:
Bonini, MARIA CHIARA; Peccatori, J; Stanghellini, Mtl; Vago, L; Bondanza, Attilio; Cieri, N; Greco, R; Bernardi, M; Corti, C; Oliveira, G; Zappone, E; Traversari, C; Bordignon, Claudio; Ciceri, Fabio
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