| Literature DB >> 26039212 |
C Bonini1, J Peccatori2, M T L Stanghellini2, L Vago2, A Bondanza1, N Cieri1, R Greco2, M Bernardi2, C Corti2, G Oliveira1, E Zappone2, C Traversari3, C Bordignon4, F Ciceri2.
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.Entities:
Mesh:
Year: 2015 PMID: 26039212 DOI: 10.1038/bmt.2015.99
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483