Phase I clinical trial of adoptive transfer of expanded natural killer cells in combination with IgG1 antibody in patients with gastric or colorectal cancer

被引:103
作者
Ishikawa, Takeshi [1 ]
Okayama, Tetsuya [1 ]
Sakamoto, Naoyuki [1 ]
Ideno, Mitsuko [2 ]
Oka, Kaname [1 ]
Enoki, Tatsuji [2 ]
Mineno, Junichi [2 ]
Yoshida, Naohisa [1 ]
Katada, Kazuhiro [1 ]
Kamada, Kazuhiro [1 ]
Uchiyama, Kazuhiko [1 ]
Handa, Osamu [1 ]
Takagi, Tomohisa [1 ]
Konishi, Hideyuki [1 ]
Kokura, Satoshi [1 ]
Uno, Kazuko [3 ]
Naito, Yuji [1 ]
Itoh, Yoshito [1 ]
机构
[1] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Gastroenterol & Hepatol, Kyoto, Japan
[2] Takara Bio Inc, CDM Ctr, Kusatsu, Japan
[3] Louis Pasteur Ctr Med Res, Div Basic Res, Kyoto, Japan
基金
日本学术振兴会;
关键词
adoptive NK therapy; antibody-dependent cellular cytotoxicity (ADCC); trastuzumab; cetuximab; REGULATORY T-CELLS; TUMOR-CELLS; OVEREXPRESSING HER2; MULTIPLE-MYELOMA; NK CELLS; THERAPY; IMMUNOTHERAPY; LENALIDOMIDE; TRASTUZUMAB; CETUXIMAB;
D O I
10.1002/ijc.31285
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Natural killer (NK) cells exhibit strong cytotoxic activity against tumor cells without prior sensitization, and have the potential to exert antibody-dependent cellular cytotoxicity (ADCC). In this clinical trial, we examined the safety and efficacy of the use of NK cells, generated using a novel expansion system, in combination with IgG1 antibodies for the treatment of advanced gastric or colorectal cancers. Treatment consisted of trastuzumab-or cetuximab-based chemotherapy, plus adoptive NK cell therapy. For administration of expanded NK cells, dose escalation with a sequential 3 + 3 design was performed in three steps, at doses of 0.5 x 10(9), 1.0 x 10(9), and 2.0 x 10(9) cells/injection (N = 9). After 3 days of IgG1 antibody administration, patients were infused with expanded NK cells three times at triweekly intervals. NK cell populations expanded with our system were confirmed as being enriched in NK cells (median 92.9%) with high expression of NKG2D (97.6%) and CD16 (69.6%). The combination therapy was very well tolerated with no severe adverse events. Among six evaluable patients, four presented stable disease (SD) and two presented progressive disease. Of the four SD patients, three showed an overall decrease in tumor size after combination therapy. Immune monitoring suggested that combination therapy enhanced whole blood IFN-production and reduced peripheral regulatory T cells (Tregs). In conclusion, this phase I trial provides evidence of good tolerability, induction of Th1 immune responses, and preliminary anti-tumor activity for this combination therapy, in patients with advanced gastric and colorectal cancer that have received previous therapy.
引用
收藏
页码:2599 / 2609
页数:11
相关论文
共 39 条
[1]   IPH2101, a novel anti-inhibitory KIR antibody, and lenalidomide combine to enhance the natural killer cell versus multiple myeloma effect [J].
Benson, Don M., Jr. ;
Bakan, Courtney E. ;
Zhang, Shuhong ;
Collins, Shauna M. ;
Liang, Jing ;
Srivastava, Shivani ;
Hofmeister, Craig C. ;
Efebera, Yvonne ;
Andre, Pascale ;
Romagne, Francois ;
Blery, Mathieu ;
Bonnafous, Cecile ;
Zhang, Jianying ;
Clever, David ;
Caligiuri, Michael A. ;
Farag, Sherif S. .
BLOOD, 2011, 118 (24) :6387-6391
[2]   Improving natural killer cell cancer immunotherapy [J].
Berrien-Elliott, Melissa M. ;
Romee, Rizwan ;
Fehniger, Todd A. .
CURRENT OPINION IN ORGAN TRANSPLANTATION, 2015, 20 (06) :671-680
[3]   A Phase I Trial to Evaluate Antibody-Dependent Cellular Cytotoxicity of Cetuximab and Lenalidomide in Advanced Colorectal and Head and Neck Cancer [J].
Bertino, Erin M. ;
McMichael, Elizabeth L. ;
Mo, Xiaokui ;
Trikha, Prashant ;
Davis, Melanie ;
Paul, Bonnie ;
Grever, Michael ;
Carson, William E. ;
Otterson, Gregory A. .
MOLECULAR CANCER THERAPEUTICS, 2016, 15 (09) :2244-2250
[4]   Fluorouracil, Leucovorin, and Oxaliplatin With and Without Cetuximab in the First-Line Treatment of Metastatic Colorectal Cancer [J].
Bokemeyer, Carsten ;
Bondarenko, Igor ;
Makhson, Anatoly ;
Hartmann, Joerg T. ;
Aparicio, Jorge ;
de Braud, Filippo ;
Donea, Serban ;
Ludwig, Heinz ;
Schuch, Gunter ;
Stroh, Christopher ;
Loos, Anja H. ;
Zubel, Angela ;
Koralewski, Piotr .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (05) :663-671
[5]   Lenalidomide plus dexamethasone for relapsed or refractory multiple myeloma [J].
Dimopoulos, Meletios ;
Spencer, Andrew ;
Attal, Michael ;
Prince, H. Miles ;
Harousseau, Jean-Luc ;
Dmoszynska, Anna ;
San Miguel, Jesus ;
Hellmann, Andrzej ;
Facon, Thierry ;
Foa, Robin ;
Corso, Alessandro ;
Masliak, Zvenyslava ;
Olesnyckyj, Marta ;
Yu, Zhinuan ;
Patin, John ;
Zeldis, Jerome B. ;
Knight, Robert D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (21) :2123-2132
[6]   Deficient expression of NCR in NK cells from acute myeloid leukemia:: evolution during leukemia treatment and impact of leukemia cells in NCRdull phenotype induction [J].
Fauriat, Cyril ;
Just-Landi, Sylvaine ;
Mallet, Francoise ;
Arnoulet, Christine ;
Sainty, Danielle ;
Olive, Daniel ;
Costello, Regis T. .
BLOOD, 2007, 109 (01) :323-330
[7]   Expansion of Highly Cytotoxic Human Natural Killer Cells for Cancer Cell Therapy [J].
Fujisaki, Hiroyuki ;
Kakuda, Harumi ;
Shimasaki, Noriko ;
Imai, Chihaya ;
Ma, Jing ;
Lockey, Timothy ;
Eldridge, Paul ;
Leung, Wing H. ;
Campana, Dario .
CANCER RESEARCH, 2009, 69 (09) :4010-4017
[8]   Pilot study of the mechanism of action of preoperative trastuzumab in patients with primary operable breast tumors overexpressing HER2 [J].
Gennari, R ;
Menard, S ;
Fagnoni, F ;
Ponchio, L ;
Scelsi, M ;
Tagliabue, E ;
Castiglioni, F ;
Villani, L ;
Magalotti, C ;
Gibelli, N ;
Oliviero, B ;
Ballardini, B ;
Da Prada, G ;
Zambelli, A ;
Costa, A .
CLINICAL CANCER RESEARCH, 2004, 10 (17) :5650-5655
[9]   The role of regulatory T cells in the control of natural killer cells: relevance during tumor progression [J].
Ghiringhelli, Francois ;
Menard, Cedric ;
Martin, Francois ;
Zitvogel, Laurence .
IMMUNOLOGICAL REVIEWS, 2006, 214 :229-238
[10]   Natural killer cell immunotherapy to target stem-like tumor cells [J].
Grossenbacher, Steven K. ;
Canter, Robert J. ;
Murphy, William J. .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2016, 4