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

被引:158
|
作者
Shah, Nina [1 ,10 ]
Li, Li [1 ]
McCarty, Jessica [1 ]
Kaur, Indreshpal [1 ]
Yvon, Eric [1 ]
Shaim, Hila [1 ]
Muftuoglu, Muharrem [1 ]
Liu, Enli [1 ]
Orlowski, Robert Z. [2 ]
Cooper, Laurence [3 ]
Lee, Dean [4 ]
Parmar, Simrit [1 ]
Cao, Kai [5 ]
Sobieiski, Catherine [6 ]
Saliba, Rima [1 ]
Hosing, Chitra [1 ]
Ahmed, Sairah [1 ]
Nieto, Yago [1 ]
Bashir, Qaiser [1 ]
Patel, Krina [1 ]
Bollard, Catherine [7 ,8 ,9 ]
Qazilbash, Muzaffar [1 ]
Champlin, Richard [1 ]
Rezvani, Katy [1 ]
Shpall, Elizabeth J. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, 1515 Holcombe Blvd,Unit 432, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma Myeloma, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Pediat, Houston, TX 77030 USA
[4] Nationwide Childrens Hosp, Dept Hematol & Oncol, Columbus, OH USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Lab Med, Houston, TX 77030 USA
[6] Columbia Univ, Inst Human Nutr, Coll Phys & Surg, New York, NY 10032 USA
[7] Childrens Natl Hlth Syst, Dept Allergy & Immunol, Washington, DC USA
[8] Childrens Natl Hlth Syst, Dept Blood & Marrow Transplantat, Washington, DC USA
[9] George Washington Univ, Washington, DC USA
[10] Univ Calif San Francisco, Dept Med, 400 Parnassus Ave,4th Floor,Box 0324, San Francisco, CA USA
关键词
myeloma; natural killer; cord blood; exvivo expansion; autologous transplant; REGULATORY T-CELLS; HLA CLASS-I; NK CELLS; DENDRITIC CELLS; HIGH-RISK; CYTOTOXICITY; LENALIDOMIDE; EXPRESSION; THERAPY; ACTIVATION;
D O I
10.1111/bjh.14570
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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 (10mg) on days -8 to -2, melphalan 200mg/m(2) 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: 5x10(6), 1x10(7), 5x10(7) and 1x10(8) 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 21months, four patients have progressed or relapsed, two of whom have died. CB-NK cells were detected invivo in six patients, with an activated phenotype (NKG2D(+)/NKp30(+)). These data warrant further development of this novel cellular therapy.
引用
收藏
页码:457 / 466
页数:10
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