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[采用CD19嵌合抗原受体T细胞疗法和异基因造血干细胞移植治疗复发的原发性中枢神经系统淋巴瘤]

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

作者信息

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

机构信息

Center for Graduate Medical Education, Okayama University Hospital.

Department of Hematology and Oncology, Okayama University Hospital.

出版信息

Rinsho Ketsueki. 2024;65(7):622-627. doi: 10.11406/rinketsu.65.622.

Abstract

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.

摘要

复发和/或难治性(R/R)原发性中枢神经系统淋巴瘤(PCNSL)预后较差。一名57岁诊断为PCNSL的男性患者通过基于大剂量甲氨蝶呤的化疗,随后进行自体造血干细胞移植(ASCT),获得了完全缓解。疾病未被治愈,因此在第三次复发后,他接受了抗CD19嵌合抗原受体(CAR)T细胞疗法tisagenlecleucel治疗。然而,CAR T细胞治疗后28天疾病再次复发。在进行第二次ASCT和单药替拉鲁替尼桥接治疗后,尝试进行异基因造血干细胞移植(allo-HSCT)作为根治性治疗。尽管获得了短暂缓解,但allo-HSCT后98天疾病复发。在allo-HSCT后复发接受替拉鲁替尼治疗期间,患者因移植相关毒性和移植后血栓性微血管病出现急性呼吸衰竭。他在allo-HSCT后175天死亡。尽管近年来对PCNSL的各种治疗方法进行了研究,但R/R PCNSL的治疗策略尚未确立。有必要进行进一步研究以改善R/R PCNSL患者的治疗结果。

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