| Literature DB >> 28295190 |
Nina Shah1, Li Li1, Jessica McCarty1, Indreshpal Kaur1, Eric Yvon1, Hila Shaim1, Muharrem Muftuoglu1, Enli Liu1, Robert Z Orlowski2, Laurence Cooper3, Dean Lee4, Simrit Parmar1, Kai Cao5, Catherine Sobieiski6, Rima Saliba1, Chitra Hosing1, Sairah Ahmed1, Yago Nieto1, Qaiser Bashir1, Krina Patel1, Catherine Bollard7, Muzaffar Qazilbash1, Richard Champlin1, Katy Rezvani1, Elizabeth J Shpall1.
Abstract
Multiple myeloma (MM) is a disease with known immune dysregulation. Natural killer (NK) cells have shown preclinical activity in MM. We conducted a first-in-human study of umbilical cord blood-derived (CB) NK cells for MM patients undergoing high dose chemotherapy and autologous haematopoietic stem cell transplantation (auto-HCT). Patients received lenalidomide (10 mg) on days -8 to -2, melphalan 200 mg/m2 on day -7, CB-NK cells on day -5 and auto-HCT on day 0. Twelve patients were enrolled, three on each of four CB-NK cell dose levels: 5 × 106 , 1 × 107 , 5 × 107 and 1 × 108 CB-NK cells/kg. Ten patients had either high-risk chromosomal changes or a history of relapsed/progressed disease. There were no infusional toxicities and no graft-versus-host disease. One patient failed to engraft due to poor autologous graft quality and was rescued with a back-up autologous graft. Overall, 10 patients achieved at least a very good partial response as their best response, including eight with near complete response or better. With a median follow-up of 21 months, four patients have progressed or relapsed, two of whom have died. CB-NK cells were detected in vivo in six patients, with an activated phenotype (NKG2D+ /NKp30+ ). These data warrant further development of this novel cellular therapy.Entities:
Keywords: autologous transplant; cord blood; ex vivo expansion; myeloma; natural killer
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Year: 2017 PMID: 28295190 PMCID: PMC5856008 DOI: 10.1111/bjh.14570
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998