错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Chimeric antigen receptor T-cell therapy after COVID-19 in refractory high-grade B-cell lymphoma

  • Kenta Hayashino,
  • Keisuke Seike,
  • Kanako Fujiwara,
  • Kaho Kondo,
  • Chisato Matsubara,
  • Toshiki Terao,
  • Wataru Kitamura,
  • Chihiro Kamoi,
  • Hideaki Fujiwara,
  • Noboru Asada,
  • Hisakazu Nishimori,
  • Daisuke Ennishi,
  • Keiko Fujii,
  • Nobuharu Fujii,
  • Ken-ichi Matsuoka,
  • Yoshinobu Maeda

摘要

Although chimeric antigen receptor T-cell (CAR-T) therapies have dramatically improved the outcomes of relapsed/refractory B-cell malignancies, recipients suffer from severe humoral immunodeficiencies. Furthermore, patients with coronavirus disease 2019 (COVID-19) have a poor prognosis, as noted in several case reports of recipients who had COVID-19 before the infusion. We report the case of a 70-year-old woman who developed COVID-19 immediately before CAR-T therapy for high-grade B-cell lymphoma. She received Tixagevimab−Cilgavimab chemotherapy and radiation therapy but never achieved remission. She was transferred to our hospital for CAR-T therapy, but developed COVID-19. Her symptoms were mild and she was treated with long-term molnupiravir. On day 28 post-infection, lymphodepleting chemotherapy was restarted after a negative polymerase chain reaction (PCR) test was confirmed. The patient did not experience recurrence of COVID-19 symptoms or severe cytokine release syndrome. Based on the analysis and comparison of the previous reports with this case, we believe that CAR-T therapy should be postponed until a negative PCR test is confirmed. In addition, Tixagevimab−Cilgavimab and long term direct-acting antiviral agent treatment can be effective prophylaxis for severe COVID-19 and shortening the duration of infection.