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First-in-man clinical trial of CAR NK-92 cells: safety test of CD33-CAR NK-92 cells in patients with relapsed and refractory acute myeloid leukemia.
Tang, Xiaowen; Yang, Lin; Li, Zheng; Nalin, Ansel P; Dai, Haiping; Xu, Ting; Yin, Jia; You, Fengtao; Zhu, Mingqing; Shen, Wenhong; Chen, Guanghua; Zhu, Xiaming; Wu, Depei; Yu, Jianhua.
Afiliación
  • Tang X; Institute of Blood and Bone Marrow Transplantation Suzhou, China.
  • Yang L; Collaborative Innovation Center of Hematology, Soochow University Suzhou, China.
  • Li Z; Collaborative Innovation Center of Hematology, Soochow University Suzhou, China.
  • Nalin AP; The Cyrus Tang Hematology Center, Soochow University Suzhou, China.
  • Dai H; Persongen BioTherapeutics Co., Ltd. Suzhou, China.
  • Xu T; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University Suzhou, China.
  • Yin J; Institute of Blood and Bone Marrow Transplantation Suzhou, China.
  • You F; Collaborative Innovation Center of Hematology, Soochow University Suzhou, China.
  • Zhu M; Comprehensive Cancer Center, The Ohio State University Columbus, OH 43210, USA.
  • Shen W; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University Suzhou, China.
  • Chen G; Institute of Blood and Bone Marrow Transplantation Suzhou, China.
  • Zhu X; Collaborative Innovation Center of Hematology, Soochow University Suzhou, China.
  • Wu D; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University Suzhou, China.
  • Yu J; Institute of Blood and Bone Marrow Transplantation Suzhou, China.
Am J Cancer Res ; 8(6): 1083-1089, 2018.
Article en En | MEDLINE | ID: mdl-30034945
ABSTRACT
CAR T cells have shown clinical efficacy for acute lymphoblastic leukemia, but this therapy has not been effective for acute myeloid leukemia (AML), and other treatment options are needed. Theoretically, CAR-NK cells have a more favorable toxicity profile compared to CAR T cells, especially in avoiding adverse effects such as cytokine release syndrome. However, the clinical evidence for this has not yet been reported. In the current study, we tested the safety of CD33-CAR NK cells in patients with relapsed and refractory AML. At doses up to 5 × 109 (5 billion) cells per patient, no significant adverse effects were observed. CAR NK-92 cells can be produced at much lower cost compared to CAR T cells, and we believe after being optimized, they will be widely accessible for the treatment of cancer.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Am J Cancer Res Año: 2018 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Am J Cancer Res Año: 2018 Tipo del documento: Article País de afiliación: China