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關于捷帕力<\/strong>®<\/sup><\/strong>(匹妥布替尼)<\/strong><\/p> \n 捷帕力®<\/sup>(匹妥布替尼,又名 LOXO-305)是一種高選擇性(在臨床前研究中,對 BTK 的選擇性比98% 的其他激酶高 300 倍)、非共價(可逆)的BTK抑制劑[6]<\/sup>。BTK 是經過驗證的分子靶標,在許多 B 細胞白血病和淋巴瘤(包括套細胞淋巴瘤)中被發現[7],[8]<\/sup>。<\/p> \n 關于套細胞淋巴瘤(<\/strong>MCL)<\/strong><\/p> \n 套細胞淋巴瘤(MCL) 是一種罕見的血液腫瘤,也是非霍奇金淋巴瘤 (NHL)的一種亞型。中國每年大約每50萬人中有一人患上 MCL。MCL 源自于 B 淋巴細胞,是一種白細胞,也是免疫系統的一部分。 MCL 通常發生于淋巴結外緣套區的 B 細胞,隨著腫瘤的進展,它會擴散到骨髓、脾臟、肝臟或消化道[9]<\/sup>。<\/p> \n 關于禮來制藥<\/strong><\/p> \n 禮來制藥是一家致力于通過科學創新改善人類健康水平,惠及全球患者的醫藥公司。作為醫療健康行業的領軍者,禮來制藥擁有近150年的歷史。今天,我們的藥物已幫助全球數千萬人。運用生物技術、化學和基因醫學的力量,我們的科學家正在積極推動新的醫學進展,以應對嚴峻的全球健康挑戰。重新定義糖尿病與肥胖療法,減少肥胖對人體的長期影響;助力阿爾茨海默病的防治行動;為一系列威脅人類健康的免疫性疾病提供解決方案;以及將難以治愈的癌癥轉變為可控的疾病。禮來制藥邁向健康世界的每一步,都源自于我們"致力于讓數百萬患者生活得更美好"的信念。這包括致力于解決全球多重挑戰的創新臨床試驗,同時確保藥物的可及性和可負擔性。如果需要了解更多關于禮來制藥的信息,請登錄:www.lilly.com。<\/p> \n [1] Nirav N. S, Wojciech J, Pier Z, et al. Pirtobrutinib in Covalent BTK-Inhibitor (cBTKi) Pre-Treated Mantle Cell Lymphoma (MCL): Updated Results and Subgroup Analysis from the Phase 1\/2 BRUIN Study with 2 Years of Survival Follow-up. Journal of Clinical Oncology, Volume 41, Number 16_suppl. doi: 10.1200\/JCO.2023.41.16_suppl.7514 若你想了解更多有關疾病知識的信息,請咨詢醫療衛生專業人士。本內容由禮來中國提供支持。審批號PP-MG-CN-3724。<\/p>"];
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[2] Michael L. W, Nirav N. S, Wojciech J, et al. Efficacy of Pirtobrutinib in Covalent BTK-Inhibitor Pre-Treated Relapsed \/ Refractory Mantle Cell Lymphoma: Additional Patients and Extended Follow-up from the Phase 1\/2 BRUIN Study. Blood (2022) 140 (Supplement 1): 9368–9372. doi: 10.1182\/blood-2022-159425
[3] Yuqin S, Shuhua Y, Haiyan Y et al. Pirtobrutinib, a Non-Covalent (Reversible) BTK Inhibitor in Mantle Cell Lymphoma Patients Previously Treated with a Covalent BTK Inhibitor: Results from a China Phase 2 Study. Blood, Volume 142, Supplement 1, 2 November 2023, Page 3636. Doi: 10.1182\/blood-2023-173287
[4] Georg H, Martin D Lucie O, Eva G, et al. Real-world experience among patients with relapsed\/refractory mantle cell lymphoma after Bruton tyrosine kinase inhibitor failure in Europe: The SCHOLAR-2 retrospective chart review study. Br J Haematol. 2022 Oct 18;202(4):749–759. doi: 10.1111\/bjh.18519. doi: 10.1111\/bjh.18519
[5] Lisa M. H, Yongmei C, Paolo B. A, et al. Outcomes among Patients with Mantle Cell Lymphoma Post-Covalent BTK Inhibitor Therapy in the United States: A Real World Electronic Medical Records Study. Adv Hematol. 2022 Dec 28:2022:8262787. doi: 10.1155\/2022\/8262787.
[6] Mato AR, Shah NN, Jurczak W, et al. Pirtobrutinib in relapsed or refractory B-cell malignancies (BRUIN): a phase 1\/2 study. Lancet. 2021;397(10277):892-901. doi:10.1016\/S0140-6736(21)00224-5
[7] Hanel W, Epperla N. Emerging therapies in mantle cell lymphoma. J Hematol Oncol. 2020;13(1):79. Published 2020 Jun 17. doi:10.1186\/s13045-020-00914-1
[8] Gu D, Tang H, Wu J, Li J, Miao Y. Targeting Bruton tyrosine kinase using non-covalent inhibitors in B cell malignancies. J Hematol Oncol. 2021;14(1):40. Published 2021 Mar 6. doi:10.1186\/s13045-021-01049-7
[9] National Organization for Rare Disorders. Mantle cell lymphoma. Accessed 26 October 2022. https:\/\/rarediseases.org\/rare-diseases\/mantle-cell-lymphoma<\/a><\/span><\/p> <\/td> \n <\/tr> \n <\/tbody> \n <\/table> \n<\/div> \n