Relapsed primary central nervous system lymphoma treated with CD19 chimeric antigen receptor T-cell therapy and allogeneic hematopoietic stem cell transplantation

Relapsed and/or refractory (R/R) primary central nervous system lymphoma (PCNSL) has a poor prognosis. A 57-year-old man diagnosed with PCNSL achieved a complete response by high-dose methotrexate-based chemotherapy followed by autologous hematopoietic stem cell transplantation (ASCT). The disease w...

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Bibliographic Details
Published in:Rinshō ketsueki Vol. 65; no. 7; p. 622
Main Authors: Fujii, Fuminari, Terao, Toshiki, Nishimori, Hisakazu, Fujii, Kentaro, Matsuo, Toshihiko, Yoshino, Tadashi, Ueda, Hiroko, Oyama, Tadashi, Matsumura, Akifumi, Kondo, Kaho, Matsubara, Chisato, Fujiwara, Kanako, Seike, Keisuke, Fujiwara, Hideaki, Asada, Noboru, Ennishi, Daisuke, Fujii, Keiko, Fujii, Nobuharu, Matsuoka, Ken-Ichi, Maeda, Yoshinobu
Format: Journal Article
Language:Japanese
Published: Japan 2024
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Summary:Relapsed and/or refractory (R/R) primary central nervous system lymphoma (PCNSL) has a poor prognosis. A 57-year-old man diagnosed with PCNSL achieved a complete response by high-dose methotrexate-based chemotherapy followed by autologous hematopoietic stem cell transplantation (ASCT). The disease was not cured, so he was treated with the anti-CD19 chimeric antigen receptor (CAR) T-cell therapy tisagenlecleucel after the third relapse. However, the disease relapsed again 28 days after CAR T-cell therapy. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) was attempted as curative therapy after bridging with second ASCT and tirabrutinib monotherapy. Although a temporary response was achieved, the disease relapsed 98 days after allo-HSCT. While receiving tirabrutinib for relapse after allo-HSCT, the patient developed acute respiratory failure due to transplant-related toxicity and post-transplant thrombotic microangiopathy. He died 175 days after allo-HSCT. Although various treatments for PCNSL have been investigated in recent years, the treatment strategy for R/R PCNSL has not been established. Further studies are warranted to improve the outcomes of patients with R/R PCNSL.
ISSN:0485-1439
DOI:10.11406/rinketsu.65.622