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病例报告:奥雷巴替尼用于急性淋巴细胞白血病移植后中枢神经系统移植后淋巴细胞增生性疾病的剂量调整。

Case Report: dose adjustment of orelabrutinib for managing central nervous system post-transplant lymphoproliferative disorder following acute lymphoblastic leukemia transplantation.

作者信息

Wang Wenwen, Chen Jianlin, Guan Lingsu

机构信息

Department of Hematology, Taizhou Central Hospital, Taizhou, China.

Department of Gastrointestinal Surgery, Taizhou Central Hospital, Taizhou, China.

出版信息

Front Immunol. 2025 Jun 26;16:1597119. doi: 10.3389/fimmu.2025.1597119. eCollection 2025.

Abstract

We report a case of acute B-cell leukemia complicated by central nervous system (CNS) post-transplant lymphoproliferative disorder (PTLD) following allogeneic hematopoietic stem cell transplantation (allo-HSCT). The patient achieved sustained disease stabilization following therapeutic dose modification of orelabrutinib, representing the first evidence-based documentation that Bruton's tyrosine kinase (BTK) inhibitor down-titration confers clinical efficacy in PTLD. Epstein-Barr virus (EBV)-associated PTLD is a serious complication following allogeneic HSCT, with frequent CNS involvement. Effective treatment for CNS involvement is often hampered by the challenge of drug penetration across the blood-brain barrier. This case highlights the potential benefit and safety of dose-adjusted orelabrutinib in controlling CNS PTLD, suggesting a promising therapeutic approach.

摘要

我们报告了一例异基因造血干细胞移植(allo-HSCT)后并发中枢神经系统(CNS)移植后淋巴细胞增殖性疾病(PTLD)的急性B细胞白血病病例。在对奥布替尼进行治疗剂量调整后,患者实现了疾病的持续稳定,这是首个基于证据的文献证明布鲁顿酪氨酸激酶(BTK)抑制剂减量在PTLD中具有临床疗效。爱泼斯坦-巴尔病毒(EBV)相关的PTLD是异基因HSCT后的一种严重并发症,常累及中枢神经系统。药物透过血脑屏障的挑战常常阻碍对中枢神经系统受累的有效治疗。该病例突出了剂量调整后的奥布替尼在控制中枢神经系统PTLD方面的潜在益处和安全性,提示了一种有前景的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b430/12240773/f00b468963a5/fimmu-16-1597119-g001.jpg

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