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用于评估替拉鲁替尼(GS-4059/ONO-4059)靶向结合的药效学的同质 BTK 占有率测定法。

Homogeneous BTK Occupancy Assay for Pharmacodynamic Assessment of Tirabrutinib (GS-4059/ONO-4059) Target Engagement.

机构信息

1 Gilead Sciences, Inc., Foster City, CA, USA.

出版信息

SLAS Discov. 2018 Oct;23(9):919-929. doi: 10.1177/2472555218786165. Epub 2018 Jul 16.

DOI:10.1177/2472555218786165
PMID:30011241
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6151956/
Abstract

Bruton's tyrosine kinase (BTK) is a clinically validated target for B-cell leukemias and lymphomas with FDA-approved small-molecule inhibitors ibrutinib and acalabrutinib. Tirabrutinib (GS-4059/ONO-4059, Gilead Sciences, Inc., Foster City, CA) is a second-generation, potent, selective, irreversible BTK inhibitor in clinical development for lymphoid malignancies, including chronic lymphocytic leukemia (CLL) and diffuse large B-cell lymphoma (DLBCL). An accurate pharmacodynamic assay to assess tirabrutinib target coverage in phase 1/2 clinical studies will inform dose and schedule selection for advanced clinical evaluation. We developed a novel duplex homogeneous BTK occupancy assay based on time-resolved fluorescence resonance energy transfer (TR-FRET) to measure free and total BTK levels in a multiplexed format. The dual-wavelength emission property of terbium-conjugated anti-BTK antibody served as the energy donor for two fluorescent energy acceptors with distinct excitation and emission spectra. The assay was characterized and qualified using full-length purified recombinant human BTK protein and peripheral blood mononuclear cells derived from healthy volunteers and patients with CLL. We demonstrated assay utility using cells derived from lymph node and bone marrow samples from patients with CLL and DLBCL. Our TR-FRET-based BTK occupancy assay provides accurate, quantitative assessment of BTK occupancy in the clinical trial program for tirabrutinib and is in use in ongoing clinical studies.

摘要

布鲁顿酪氨酸激酶 (BTK) 是一种经临床验证的 B 细胞白血病和淋巴瘤靶点,已有 FDA 批准的小分子抑制剂伊布替尼和阿卡替尼。替拉鲁替尼 (GS-4059/ONO-4059,吉利德科学公司,福斯特市,加利福尼亚州) 是一种正在临床开发用于淋巴恶性肿瘤的第二代、有效、选择性、不可逆 BTK 抑制剂,包括慢性淋巴细胞白血病 (CLL) 和弥漫性大 B 细胞淋巴瘤 (DLBCL)。在 1/2 期临床研究中,一种准确的药效学测定法可评估替拉鲁替尼的靶标覆盖范围,为高级临床评估提供剂量和方案选择。我们开发了一种基于时间分辨荧光共振能量转移 (TR-FRET) 的新型双相合 BTK 占有率测定法,以在多重格式下测量游离和总 BTK 水平。铽标记抗 BTK 抗体的双波长发射特性用作两个荧光能受体的能量供体,它们具有不同的激发和发射光谱。该测定法使用全长纯化重组人 BTK 蛋白和源自健康志愿者和 CLL 患者的外周血单核细胞进行了表征和合格验证。我们使用源自 CLL 和 DLBCL 患者的淋巴结和骨髓样本的细胞证明了该测定法的实用性。我们基于 TR-FRET 的 BTK 占有率测定法为替拉鲁替尼的临床试验计划提供了准确、定量的 BTK 占有率评估,并且正在进行中的临床研究中使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/3a42ceda65e8/10.1177_2472555218786165-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/86b332f10a66/10.1177_2472555218786165-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/59f40a713d95/10.1177_2472555218786165-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/769f2185bdee/10.1177_2472555218786165-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/033c037e34ca/10.1177_2472555218786165-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/057f84ee7d0e/10.1177_2472555218786165-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/3a42ceda65e8/10.1177_2472555218786165-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/86b332f10a66/10.1177_2472555218786165-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/59f40a713d95/10.1177_2472555218786165-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/769f2185bdee/10.1177_2472555218786165-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/033c037e34ca/10.1177_2472555218786165-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/057f84ee7d0e/10.1177_2472555218786165-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4510/6151956/3a42ceda65e8/10.1177_2472555218786165-fig6.jpg

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本文引用的文献

1
Acalabrutinib in relapsed or refractory mantle cell lymphoma (ACE-LY-004): a single-arm, multicentre, phase 2 trial.阿卡替尼治疗复发或难治性套细胞淋巴瘤(ACE-LY-004):一项单臂、多中心、2 期临床试验。
Lancet. 2018 Feb 17;391(10121):659-667. doi: 10.1016/S0140-6736(17)33108-2. Epub 2017 Dec 11.
2
Chronic lymphocytic leukaemia.慢性淋巴细胞白血病。
Nat Rev Dis Primers. 2017 Jan 19;3:16096. doi: 10.1038/nrdp.2016.96.
3
Acalabrutinib (ACP-196) in Relapsed Chronic Lymphocytic Leukemia.阿卡替尼(ACP-196)用于复发的慢性淋巴细胞白血病
半机械论 PK/PD 模型与模拟不可逆 BTK 抑制作用,支持替拉鲁替尼在 RA 受试者中的剂量选择。
Clin Pharmacol Ther. 2022 Feb;111(2):416-424. doi: 10.1002/cpt.2439. Epub 2021 Oct 27.
4
Target modulation and pharmacokinetics/pharmacodynamics translation of the BTK inhibitor poseltinib for model-informed phase II dose selection.布鲁顿酪氨酸激酶(BTK)抑制剂泊昔替尼的靶点调控及药代动力学/药效学转化,用于模型引导的II期剂量选择
Sci Rep. 2021 Sep 21;11(1):18671. doi: 10.1038/s41598-021-98255-7.
5
Bleeding by Bruton Tyrosine Kinase-Inhibitors: Dependency on Drug Type and Disease.布鲁顿酪氨酸激酶抑制剂导致的出血:对药物类型和疾病的依赖性
Cancers (Basel). 2021 Mar 4;13(5):1103. doi: 10.3390/cancers13051103.
6
A novel tricyclic BTK inhibitor suppresses B cell responses and osteoclastic bone erosion in rheumatoid arthritis.一种新型三环 BTK 抑制剂抑制类风湿关节炎中 B 细胞反应和破骨细胞骨侵蚀。
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4
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7
Ibrutinib versus ofatumumab in previously treated chronic lymphoid leukemia.伊布替尼与奥法妥木单抗治疗既往治疗的慢性淋巴细胞白血病。
N Engl J Med. 2014 Jul 17;371(3):213-23. doi: 10.1056/NEJMoa1400376. Epub 2014 May 31.
8
Targeting Bruton's tyrosine kinase in B cell malignancies.针对 B 细胞恶性肿瘤的布鲁顿酪氨酸激酶。
Nat Rev Cancer. 2014 Apr;14(4):219-32. doi: 10.1038/nrc3702.
9
Ibrutinib as initial therapy for elderly patients with chronic lymphocytic leukaemia or small lymphocytic lymphoma: an open-label, multicentre, phase 1b/2 trial.伊布替尼作为初治老年慢性淋巴细胞白血病或小淋巴细胞淋巴瘤患者的治疗方案:一项开放标签、多中心、1b/2 期临床试验。
Lancet Oncol. 2014 Jan;15(1):48-58. doi: 10.1016/S1470-2045(13)70513-8. Epub 2013 Dec 10.
10
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Leuk Res. 2013 Oct;37(10):1271-7. doi: 10.1016/j.leukres.2013.07.028. Epub 2013 Aug 17.