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Safety and efficacy of chimeric antigen receptor (CAR)-T-cell therapy in persons with advanced B-cell cancers and hepatitis B virus-infection.

Ying WangYang LiuXu TanBin PanJian GeKunming QiHai ChengJiang CaoMing ShiZhiling YanJianlin QiaoGuangjun JingXue WangWei SangRuixiang XiaXi ZhangZhenyu LiRobert Peter GaleJun-Nian ZhengFeng ZhuKailin Xu
Published in: Leukemia (2020)
Chimeric antigen receptor (CAR)-T-cell is a safe and effective therapy of B-cell cancers but it is unknown if this is so in persons with prior hepatitis B virus (HBV) infection. We studied 70 subjects with advanced B-cell cancers receiving CAR-T-cell therapy, 12 of whom had chronic HBV-infection (HBsAg positive) and 29 with resolved HBV-infection (HBsAg negative and anti-HBc positive). Safety and efficacy were compared with 29 subjects without HBV-infection. HBV was reactivated in 2 subjects with chronic HBV-infection and 1 with resolved HBV-infection. There was no HBV-related hepatitis flare. Responses to CAR-T-cell therapy in the three cohorts were not significantly different. There was no significant difference in the incidence or severity of cytokine release syndrome (CRS) and neurologic toxicity between the cohorts. Our data suggest that chronic and resolved HBV-infection do not affect the safety and efficacy of CAR-T-cell therapy.
Keyphrases
  • hepatitis b virus
  • cell therapy
  • liver failure
  • stem cells
  • mesenchymal stem cells
  • single cell
  • oxidative stress
  • machine learning
  • deep learning
  • drug induced
  • big data
  • artificial intelligence
  • solid state