作者
Nina Shah,Li Li,Jessica M McCarty,Indreshpal Kaur,Eric Yvon,Hila Shaim,Muharrem Müftüoǧlu,Enli Liu,Robert Z. Orlowski,Laurence J.N. Cooper,Dean A. Lee,Simrit Parmar,Kai Cao,Catherine Sobieiski,Rima M. Saliba,Chitra Hosing,Sairah Ahmed,Yago Nieto,Qaiser Bashir,Krina K. Patel,Catherine M. Bollard,Muzaffar H. Qazilbash,Richard E. Champlin,Katy Rezvani,Elizabeth J. Shpall
摘要
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.