| Literature DB >> 26325439 |
Eric Smith1, Sean M Devlin2, Satyajit Kosuri1, Evelyn Orlando3, Heather Landau4, Alex M Lesokhin5, David J Chung4, Hani Hassoun5, Nikoletta Lendvai5, Ola Landgren5, Sergio Giralt4, Ajai Chari6, Sundar Jagannath6, Guenther Koehne7.
Abstract
We report results of a retrospective analysis of 44 patients with relapsed and high-risk multiple myeloma (MM) undergoing allogeneic CD34-selected hematopoietic stem cell transplantation (HSCT) from HLA-compatible donors. Patients had multiply relapsed disease including relapse at <15 months after autologous transplantation and most patients (28 of 44; 65%) also had high-risk cytogenetics. Before transplantation, patients received busulfan (.8 mg/kg × 10 doses), melphalan (70 mg/m(2) × 2 days), fludarabine (25 mg/m(2) × 5 days), and rabbit antithymocyte globulin (2.5 mg/kg × 2 days). Patients with 10/10 HLA- matched donors were treated prophylactically with low doses of donor lymphocyte infusions (.5 to 1 × 10(6) CD3(+)/kg) starting 4 to 6 months after CD34-selected HSCT. Acute (grade II to IV) graft-versus-host disease (GVHD) and transplantation-related mortality at 12 months were 2% and 18%, respectively. Chronic GVHD was not observed in any patient. Overall and progression-free survival at 2 years were 54% and 31%, respectively. By multivariate analyses, the outcomes of CD34-selected HSCT were influenced by presence of extramedullary disease, disease status before CD34-selected HSCT, and age. This study demonstrates notable safety and efficacy of CD34-selected HSCT in patients with multiply relapsed MM, including those with high-risk cytogenetics.Entities:
Keywords: Adoptive immunotherapy; D34-selected hematopoietic stem cell transplantation; Relapsed high-risk multiple myeloma
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Year: 2015 PMID: 26325439 PMCID: PMC4975432 DOI: 10.1016/j.bbmt.2015.08.025
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742