CAR T-cell therapy for gastric cancer: Potential and perspective (Review)

被引:16
作者
Long, Bo [1 ]
Qin, Long [2 ]
Zhang, Boya [1 ]
Li, Qiong [3 ]
Wang, Long [1 ]
Jiang, Xiangyan [1 ]
Ye, Huili [2 ]
Zhang, Genyuan [1 ]
Yu, Zeyuan [1 ]
Jiao, Zuoyi [1 ]
机构
[1] Lanzhou Univ, Hosp 2, Dept Gen Surg 1, 82 Cuiying Gate, Lanzhou 730000, Gansu, Peoples R China
[2] Lanzhou Univ, Hosp 2, Cuiying Ctr, Lanzhou 730000, Gansu, Peoples R China
[3] Lanzhou Univ, Hosp 1, Dept Endocrinol, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
chimeric antigen receptor-T cell; gastric cancer; immunotherapy; solid tumor; CHIMERIC-ANTIGEN-RECEPTOR; ADOPTIVE IMMUNOTHERAPY; CYTOKINE RELEASE; TUMOR MICROENVIRONMENT; CLINICAL-TRIAL; PERSISTENCE; LYMPHOMA; REMISSIONS; TOXICITIES; CHALLENGES;
D O I
10.3892/ijo.2020.4982
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gastric cancer (GC) is one of the most frequently diagnosed digestive malignancies and is the third leading cause of cancer-associated death worldwide. Delayed diagnosis and poor prognosis indicate the urgent need for new therapeutic strategies. The success of chimeric antigen receptor (CAR) T-cell therapy for chemotherapy-refractory hematological malignancies has inspired the development of a similar strategy for GC treatment. Although using CAR T-cells against GC is not without difficulty, results from preclinical studies remain encouraging. The current review summarizes relevant preclinical studies and ongoing clinical trials for the use of CAR T-cells for GC treatment and investigates possible toxicities, as well as current clinical experiences and emerging approaches. With a deeper understanding of the tumor microenvironment, novel target epitopes and scientific-technical progress, the potential of CAR T-cell therapy for GC is anticipated in the near future.
引用
收藏
页码:889 / 899
页数:11
相关论文
共 103 条
[1]   T cells expressing an anti-B-cell maturation antigen chimeric antigen receptor cause remissions of multiple myeloma [J].
Ali, Syed Abbas ;
Shi, Victoria ;
Maric, Irina ;
Wang, Michael ;
Stroncek, David F. ;
Rose, Jeremy J. ;
Brudno, Jennifer N. ;
Stetler-Stevenson, Maryalice ;
Feldman, Steven A. ;
Hansen, Brenna G. ;
Fellowes, Vicki S. ;
Hakim, Frances T. ;
Gress, Ronald E. ;
Kochenderfer, James N. .
BLOOD, 2016, 128 (13) :1688-1700
[2]   Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries [J].
Allemani, Claudia ;
Matsuda, Tomohiro ;
Di Carlo, Veronica ;
Harewood, Rhea ;
Matz, Melissa ;
Niksic, Maja ;
Bonaventure, Audrey ;
Valkov, Mikhail ;
Johnson, Christopher J. ;
Esteve, Jacques ;
Ogunbiyi, Olufemi J. ;
Azevedo e Silva, Gulnar ;
Chen, Wan-Qing ;
Eser, Sultan ;
Engholm, Gerda ;
Stiller, Charles A. ;
Monnereau, Alain ;
Woods, Ryan R. ;
Visser, Otto ;
Lim, Gek Hsiang ;
Aitken, Joanne ;
Weir, Hannah K. ;
Coleman, Michel P. .
LANCET, 2018, 391 (10125) :1023-1075
[3]  
[Anonymous], BREAST CANCER RES
[4]   Chimeric antigen receptor-modified T cells for the treatment of solid tumors: Defining the challenges and next steps [J].
Beatty, Gregory L. ;
O'Hara, Mark .
PHARMACOLOGY & THERAPEUTICS, 2016, 166 :30-39
[5]   CD19-Targeted T Cells Rapidly Induce Molecular Remissions in Adults with Chemotherapy-Refractory Acute Lymphoblastic Leukemia [J].
Brentjens, Renier J. ;
Davila, Marco L. ;
Riviere, Isabelle ;
Park, Jae ;
Wang, Xiuyan ;
Cowell, Lindsay G. ;
Bartido, Shirley ;
Stefanski, Jolanta ;
Taylor, Clare ;
Olszewska, Malgorzata ;
Borquez-Ojeda, Oriana ;
Qu, Jinrong ;
Wasielewska, Teresa ;
He, Qing ;
Bernal, Yvette ;
Rijo, Ivelise V. ;
Hedvat, Cyrus ;
Kobos, Rachel ;
Curran, Kevin ;
Steinherz, Peter ;
Jurcic, Joseph ;
Rosenblat, Todd ;
Maslak, Peter ;
Frattini, Mark ;
Sadelain, Michel .
SCIENCE TRANSLATIONAL MEDICINE, 2013, 5 (177)
[6]   Safety and persistence of adoptively transferred autologous CD19-targeted T cells in patients with relapsed or chemotherapy refractory B-cell leukemias [J].
Brentjens, Renier J. ;
Riviere, Isabelle ;
Park, Jae H. ;
Davila, Marco L. ;
Wang, Xiuyan ;
Stefanski, Jolanta ;
Taylor, Clare ;
Yeh, Raymond ;
Bartido, Shirley ;
Borquez-Ojeda, Oriana ;
Olszewska, Malgorzata ;
Bernal, Yvette ;
Pegram, Hollie ;
Przybylowski, Mark ;
Hollyman, Daniel ;
Usachenko, Yelena ;
Pirraglia, Domenick ;
Hosey, James ;
Santos, Elmer ;
Halton, Elizabeth ;
Maslak, Peter ;
Scheinberg, David ;
Jurcic, Joseph ;
Heaney, Mark ;
Heller, Glenn ;
Frattini, Mark ;
Sadelain, Michel .
BLOOD, 2011, 118 (18) :4817-4828
[7]   SIGNALS THROUGH T-CELL RECEPTOR-ZETA CHAIN ALONE ARE INSUFFICIENT TO PRIME RESTING T-LYMPHOCYTES [J].
BROCKER, T ;
KARJALAINEN, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1653-1659
[8]   Bioactivity and Safety of IL13Rα2-Redirected Chimeric Antigen Receptor CD8+ T Cells in Patients with Recurrent Glioblastoma [J].
Brown, Christine E. ;
Badie, Behnam ;
Barish, Michael E. ;
Weng, Lihong ;
Ostberg, Julie R. ;
Chang, Wen-Chung ;
Naranjo, Araceli ;
Starr, Renate ;
Wagner, Jamie ;
Wright, Christine ;
Zhai, Yubo ;
Bading, James R. ;
Ressler, Julie A. ;
Portnow, Jana ;
D'Apuzzo, Massimo ;
Forman, Stephen J. ;
Jensen, Michael C. .
CLINICAL CANCER RESEARCH, 2015, 21 (18) :4062-4072
[9]   Recent advances in CAR T-cell toxicity: Mechanisms, manifestations and management [J].
Brudno, Jennifer N. ;
Kochenderfer, James N. .
BLOOD REVIEWS, 2019, 34 :45-55
[10]   T Cells Genetically Modified to Express an Anti-B-Cell Maturation Antigen Chimeric Antigen Receptor Cause Remissions of Poor-Prognosis Relapsed Multiple Myeloma [J].
Brudno, Jennifer N. ;
Maric, Irina ;
Hartman, Steven D. ;
Rose, Jeremy J. ;
Wang, Michael ;
Lam, Norris ;
Stetler-Stevenson, Maryalice ;
Salem, Dalia ;
Yuan, Constance ;
Pavletic, Steven ;
Kanakry, Jennifer A. ;
Ali, Syed Abbas ;
Mikkilineni, Lekha ;
Feldman, Steven A. ;
Stroncek, David F. ;
Hansen, Brenna G. ;
Lawrence, Judith ;
Patel, Rashmika ;
Hakim, Frances ;
Gress, Ronald E. ;
Kochenderfer, James N. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (22) :2267-+