Phase I study of cord blood-derived natural killer cells combined with autologous stem cell transplantation in multiple myeloma

Nina Shah(The University of Texas MD Anderson Cancer Center), Li Li(The University of Texas MD Anderson Cancer Center), Jessica M McCarty(The University of Texas MD Anderson Cancer Center), Indreshpal Kaur(The University of Texas MD Anderson Cancer Center), Eric Yvon(The University of Texas MD Anderson Cancer Center), Hila Shaim(The University of Texas MD Anderson Cancer Center), Muharrem Müftüoğlu(The University of Texas MD Anderson Cancer Center), Enli Liu(The University of Texas MD Anderson Cancer Center), Robert Z. Orlowski(The University of Texas MD Anderson Cancer Center), Laurence J.N. Cooper(The University of Texas MD Anderson Cancer Center), Dean A. Lee(Nationwide Children's Hospital), Simrit Parmar(The University of Texas MD Anderson Cancer Center), Kai Cao(The University of Texas MD Anderson Cancer Center), Catherine Sobieiski(Columbia University), Rima M. Saliba(The University of Texas MD Anderson Cancer Center), Chitra Hosing(The University of Texas MD Anderson Cancer Center), Sairah Ahmed(The University of Texas MD Anderson Cancer Center), Yago Nieto(The University of Texas MD Anderson Cancer Center), Qaiser Bashir(The University of Texas MD Anderson Cancer Center), Krina K. Patel(The University of Texas MD Anderson Cancer Center), Catherine M. Bollard(Children's National), Muzaffar H. Qazilbash(The University of Texas MD Anderson Cancer Center), Richard E. Champlin(The University of Texas MD Anderson Cancer Center), Katy Rezvani(The University of Texas MD Anderson Cancer Center), Elizabeth J. Shpall(The University of Texas MD Anderson Cancer Center)
British Journal of Haematology
March 14, 2017
Cited by 221Open Access
Full Text

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.


Related Papers

No related papers found

Powered by citation graph analysis