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伊布替尼治疗新诊断的原发性中枢神经系统淋巴瘤老年患者的长期生存情况

Long-Term Survival with Ibrutinib Therapy in Elderly Patients with Newly Diagnosed Primary Central Nervous System Lymphoma.

作者信息

Kuhlman Justin J, Alhaj Moustafa Muhamad, Jiang Liuyan, Wang Jing, Gupta Vivek, Tun Han W

机构信息

Department of Internal Medicine, Mayo Clinic, Jacksonville, FL, USA.

Division of Hematology and Oncology, Mayo Clinic, Jacksonville, FL, USA.

出版信息

Blood Lymphat Cancer. 2022 Apr 14;12:23-29. doi: 10.2147/BLCTT.S360442. eCollection 2022.

DOI:10.2147/BLCTT.S360442
PMID:35444484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9015786/
Abstract

Primary central nervous system lymphoma (PCNSL) carries a dismal prognosis in elderly patients above 70 years of age with a median overall survival of 6 months. Novel therapeutic agents are urgently needed to improve survival outcomes in this age group. We describe the clinical presentation, diagnostic workup, and treatment outcome in two 80-year-old patients diagnosed with PCNSL who were treated with ibrutinib therapy. Both patients remain in complete remission following treatment with ibrutinib therapy. One patient is currently 4 years and the other is 2 years and 9 months from the time of initial diagnosis. We suggest that ibrutinib therapy has significant therapeutic activity against PCNSL in the newly diagnosed setting and should be evaluated in a clinical trial as part of front-line therapy, especially in elderly patients.

摘要

原发性中枢神经系统淋巴瘤(PCNSL)在70岁以上老年患者中的预后不佳,中位总生存期为6个月。迫切需要新型治疗药物来改善该年龄组的生存结果。我们描述了两名80岁确诊为PCNSL并接受依鲁替尼治疗的患者的临床表现、诊断检查和治疗结果。两名患者在接受依鲁替尼治疗后均处于完全缓解状态。一名患者自初次诊断起已存活4年,另一名患者已存活2年9个月。我们认为,依鲁替尼治疗在新诊断的PCNSL患者中具有显著的治疗活性,应在临床试验中作为一线治疗的一部分进行评估,尤其是在老年患者中。

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Eur J Cancer. 2019 Aug;117:121-130. doi: 10.1016/j.ejca.2019.05.024. Epub 2019 Jul 3.
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Central Nervous System Lymphoma.中枢神经系统淋巴瘤。
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Introduction of novel agents in the treatment of primary CNS lymphoma.
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The elderly left behind-changes in survival trends of primary central nervous system lymphoma over the past 4 decades.被遗忘的老年人——过去 40 年原发性中枢神经系统淋巴瘤生存趋势的变化。
Neuro Oncol. 2018 Apr 9;20(5):687-694. doi: 10.1093/neuonc/nox187.
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