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Comparation of CART19 and autologous stem-cell transplantation for refractory/relapsed non-Hodgkin's lymphoma.
Li, Caixia; Zhang, Ying; Zhang, Changfeng; Chen, Jia; Lou, Xiaoyan; Chen, Xiaochen; Kang, Liqing; Xu, Nan; Li, Minghao; Tan, Jingwen; Sun, Xiuli; Zhou, Jin; Yang, Zhen; Zong, Xiangping; Wang, Pu; Xu, Ting; Qu, Changju; Huang, Haiwen; Jin, Zhengming; Yu, Lei; Wu, Depei.
Affiliation
  • Li C; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Zhang Y; Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
  • Zhang C; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Chen J; Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
  • Lou X; UniCar Therapy Ltd., Shanghai, China.
  • Chen X; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Kang L; Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
  • Xu N; UniCar Therapy Ltd., Shanghai, China.
  • Li M; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Tan J; Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
  • Sun X; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China.
  • Zhou J; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China.
  • Yang Z; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China.
  • Zong X; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China.
  • Wang P; UniCar Therapy Ltd., Shanghai, China.
  • Xu T; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Qu C; Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
  • Huang H; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Jin Z; Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
  • Yu L; Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Wu D; Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, Jiangsu, China.
JCI Insight ; 52019 07 23.
Article in En | MEDLINE | ID: mdl-31335321
ABSTRACT

BACKGROUND:

Autologous stem-cell transplantation (ASCT) is the standard treatment for R/R B-NHL, while chimeric antigen receptor T (CAR-T) therapy targeting CD19 emerges as an alternative strategy. Here we report a comparative analysis of the two strategies in a single center.

METHODS:

We performed a prospective single-arm study of CAR-T therapy in 29 patients with R/R B-NHL and compared the outcomes with contemporaneous 27 patients who received ASCT. NHL was diagnosed by histopathological assessments, and the safety and efficacy were compared.

RESULTS:

The CAR-T group exhibited better rates of CR (48.0% vs. 20.8%, P=0.046) and one-year OS (74.4% vs. 44.5%, P=0.044) compared with the ASCT group. Subpopulation analysis showed that patients with IPI scores ≥ 3 achieved significantly higher ORR and CR rates in the CAR-T group than in the ASCT group (ORR 72.0% vs. 10.0%, P=0.002; CR 38.9% vs 0% P=0.030, respectively). The most common severe adverse events in the CAR-T group were cytokine release syndrome, neurotoxicity and infection compared with cytopenia, gastrointestinal toxicity and infection in the ASCT group. Additionally, the incidence of non-hematologic severe adverse events (SAEs) was markedly lower in the CAR-T group than in the ASCT group (20.7% vs. 48.1% P=0.030).

CONCLUSION:

CAR-T therapy exhibited superior clinical outcomes in safety and efficacy over ASCT in patients with R/R B-NHL, suggesting CAR-T may be a recommended alternative to ASCT.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transplantation, Autologous / Lymphoma, Non-Hodgkin / Receptors, Antigen, T-Cell / Immunotherapy, Adoptive / Hematopoietic Stem Cell Transplantation Type of study: Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: JCI Insight Year: 2019 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transplantation, Autologous / Lymphoma, Non-Hodgkin / Receptors, Antigen, T-Cell / Immunotherapy, Adoptive / Hematopoietic Stem Cell Transplantation Type of study: Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: JCI Insight Year: 2019 Document type: Article Affiliation country: China