Kai Cao, Elizabeth J Shpall, Katy Rezvani, Richard Champlin, Muzaffar Qazilbash, Catherine Bollard, Krina Patel, Qaiser Bashir, Yago Nieto, Sairah Ahmed, Chitra Hosing, Rima Saliba, Catherine Sobieiski, Nina Shah, Simrit Parmar, Dean Lee, Laurence Cooper, Robert Z Orlowski, Enli Liu, Muharrem Muftuoglu, Hila Shaim, Eric Yvon, Indreshpal Kaur, Jessica McCarty, Li Li
Journal: British journal of haematology 2017;177(3):457-466
PMID: 28295190
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/m 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 × 10 , 1 × 10 , 5 × 10 and 1 × 10 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.
© 2017 John Wiley & Sons Ltd.
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