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AZD4547 是一种 FGFR 抑制剂,在激素抵抗性乳腺癌中开展的 IIa 期 RADICAL 试验结果。

Results of the phase IIa RADICAL trial of the FGFR inhibitor AZD4547 in endocrine resistant breast cancer.

机构信息

Department of Surgery and Cancer, Imperial College London, London, UK.

Cancer Research UK Clinical Trials Unit, Beatson West of Scotland Cancer Centre, Glasgow, UK.

出版信息

Nat Commun. 2022 Jun 10;13(1):3246. doi: 10.1038/s41467-022-30666-0.

DOI:10.1038/s41467-022-30666-0
PMID:35688802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9187670/
Abstract

We conducted a phase IIa, multi-centre, open label, single arm study (RADICAL; NCT01791985) of AZD4547 (a potent and selective inhibitor of Fibroblast Growth Factor Receptor (FGFR)-1, 2 and 3 receptor tyrosine kinases) administered with anastrozole or letrozole in estrogen receptor positive metastatic breast cancer patients who had become resistant to aromatase inhibitors. After a safety run-in study to assess safety and tolerability, we recruited 52 patients. The primary endpoint was change in tumour size at 12 weeks, and secondary endpoints were to assess response at 6 weeks, 20 weeks and every 8 weeks thereafter and tolerability of the combined treatment. Two partial responses (PR) and 19 stable disease (SD) patients were observed at the 12-week time point. At 28 weeks, according to centrally reviewed Response Evaluation Criteria in Solid Tumours (RECIST) criteria, five PR and 8 SD patients were observed in 50 assessable cases. Overall, objective response rate (5 PR) was of 10%, meeting the pre-specified endpoint. Fourteen patients discontinued due to adverse events. Eleven patients had retinal pigment epithelial detachments which was asymptomatic and reversible in all but one patient. Exploratory ribonucleic acid sequencing (RNA-Seq) analysis was done on patients' samples: 6 differentially-expressed-genes could distinguish those who benefited from the addition of AZD4547.

摘要

我们开展了一项多中心、开放标签、单臂的 IIa 期研究(RADICAL;NCT01791985),评估了在对芳香化酶抑制剂耐药的雌激素受体阳性转移性乳腺癌患者中,阿得贝利单抗(一种强效和选择性的成纤维细胞生长因子受体(FGFR)-1、2 和 3 受体酪氨酸激酶抑制剂)联合阿那曲唑或来曲唑的疗效。在进行安全性探索性研究以评估安全性和耐受性后,我们招募了 52 名患者。主要终点是 12 周时肿瘤大小的变化,次要终点是评估 6 周、20 周和此后每 8 周的反应以及联合治疗的耐受性。在 12 周时,有 2 名部分缓解(PR)和 19 名疾病稳定(SD)患者。根据实体瘤反应评价标准(RECIST),在 50 可评估病例中,有 5 名 PR 和 8 名 SD 患者在 28 周时观察到。总的来说,客观缓解率(5 名 PR)为 10%,达到了预设的终点。14 名患者因不良事件而停药。11 名患者出现视网膜色素上皮脱离,除 1 名患者外,所有患者均无症状且可逆转。对患者样本进行了探索性 RNA 测序(RNA-Seq)分析:6 个差异表达基因可以区分出从联合治疗中获益的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e9/9187670/3f1286759c93/41467_2022_30666_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e9/9187670/ff675dcfd6b6/41467_2022_30666_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e9/9187670/39c59487ff26/41467_2022_30666_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e9/9187670/3f1286759c93/41467_2022_30666_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e9/9187670/ff675dcfd6b6/41467_2022_30666_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e9/9187670/39c59487ff26/41467_2022_30666_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e9/9187670/3f1286759c93/41467_2022_30666_Fig3_HTML.jpg

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Biochim Biophys Acta Rev Cancer. 2021 Dec;1876(2):188595. doi: 10.1016/j.bbcan.2021.188595. Epub 2021 Jul 23.
2
Acquired FGFR and FGF Alterations Confer Resistance to Estrogen Receptor (ER) Targeted Therapy in ER Metastatic Breast Cancer.获得性 FGFR 和 FGF 改变赋予 ER 转移性乳腺癌对雌激素受体(ER)靶向治疗的耐药性。
Clin Cancer Res. 2020 Nov 15;26(22):5974-5989. doi: 10.1158/1078-0432.CCR-19-3958. Epub 2020 Jul 28.
3
成纤维细胞生长因子受体信号传导以SOAT1依赖的方式调节胆固醇储存,以促进乳腺肿瘤细胞侵袭。
Breast Cancer Res. 2025 Jul 15;27(1):132. doi: 10.1186/s13058-025-02084-9.
4
Phase Ib Trial of Fulvestrant, Palbociclib and Erdafitinib, a pan-FGFR Tyrosine Kinase Inhibitor, in HR+/HER2- Metastatic Breast Cancer.氟维司群、哌柏西利和泛FGFR酪氨酸激酶抑制剂厄达替尼用于HR+/HER2-转移性乳腺癌的Ib期试验。
Clin Cancer Res. 2025 Jul 8. doi: 10.1158/1078-0432.CCR-24-3803.
5
MicroRNAs as Sensitizers of Tyrosine Kinase Inhibitor Resistance in Cancer: Small Molecule Partnerships.微小RNA作为癌症中酪氨酸激酶抑制剂耐药的增敏剂:小分子合作伙伴关系
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7
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8
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9
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Contemp Oncol (Pozn). 2024;28(4):341-349. doi: 10.5114/wo.2024.147003. Epub 2025 Jan 15.
10
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J Biomed Sci. 2025 Jan 9;32(1):7. doi: 10.1186/s12929-024-01099-2.
Lucitanib for the Treatment of HR/HER2 Metastatic Breast Cancer: Results from the Multicohort Phase II FINESSE Study.
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