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依维莫司联合卡培他滨和替莫唑胺治疗神经内分泌肿瘤的安全性和有效性的多中心、开放标签、单臂Ⅱ期临床试验

Clinical Evaluation of the Effect of Encorafenib on Bupropion, Rosuvastatin, and Coproporphyrin I and Considerations for Statin Coadministration.

机构信息

Pfizer Inc, San Diego, CA, USA.

Pfizer Inc, Boulder, CO, USA.

出版信息

Clin Pharmacokinet. 2024 Apr;63(4):483-496. doi: 10.1007/s40262-024-01352-9. Epub 2024 Feb 29.

Abstract

BACKGROUND AND OBJECTIVES

Encorafenib is a kinase inhibitor indicated for the treatment of patients with unresectable or metastatic melanoma or metastatic colorectal cancer, respectively, with selected BRAF V600 mutations. A clinical drug-drug interaction (DDI) study was designed to evaluate the effect of encorafenib on rosuvastatin, a sensitive substrate of OATP1B1/3 and breast cancer resistance protein (BCRP), and bupropion, a sensitive CYP2B6 substrate. Coproporphyrin I (CP-I), an endogenous substrate for OATP1B1, was measured in a separate study to deconvolute the mechanism of transporter DDI.

METHODS

DDI study participants received a single oral dose of rosuvastatin (10 mg) and bupropion (75 mg) on days - 7, 1, and 14 and continuous doses of encorafenib (450 mg QD) and binimetinib (45 mg BID) starting on day 1. The CP-I data were collected from participants in a phase 3 study who received encorafenib (300 mg QD) and cetuximab (400 mg/m initial dose, then 250 mg/m QW). Pharmacokinetic and pharmacodynamic analysis was performed using noncompartmental and compartmental methods.

RESULTS

Bupropion exposure was not increased, whereas rosuvastatin C and area under the receiver operating characteristic curve (AUC) increased approximately 2.7 and 1.6-fold, respectively, following repeated doses of encorafenib and binimetinib. Increase in CP-I was minimal, suggesting that the primary effect of encorafenib on rosuvastatin is through BCRP. Categorization of statins on the basis of their metabolic and transporter profile suggests pravastatin would have the least potential for interaction when coadministered with encorafenib.

CONCLUSION

The results from these clinical studies suggest that encorafenib does not cause clinically relevant CYP2B6 induction or inhibition but is an inhibitor of BCRP and may also inhibit OATP1B1/3 to a lesser extent. Based on these results, it may be necessary to consider switching statins or reducing statin dosage accordingly for coadministration with encorafenib.

CLINICAL TRIAL REGISTRATION

ClinicalTrials.gov NCT03864042, registered 6 March 2019.

摘要

背景和目的

依维莫司是一种激酶抑制剂,分别用于治疗不可切除或转移性黑色素瘤或转移性结直肠癌患者,这些患者均有选择的 BRAF V600 突变。一项临床药物-药物相互作用(DDI)研究旨在评估依维莫司对rosuvastatin 的影响,rosuvastatin 是 OATP1B1/3 和乳腺癌耐药蛋白(BCRP)的敏感底物,以及 bupropion,一种敏感的 CYP2B6 底物。在一项单独的研究中,测定了内源性 OATP1B1 底物 coproporphyrin I (CP-I),以解析转运蛋白 DDI 的机制。

方法

DDI 研究参与者于第-7、1 和 14 天分别接受一次口服 rosuvastatin(10mg)和 bupropion(75mg),并于第 1 天开始连续给予依维莫司(450mg QD)和 binimetinib(45mg BID)。CP-I 数据来自接受依维莫司(300mg QD)和 cetuximab(初始剂量 400mg/m,然后 250mg/m QW)的 3 期研究的参与者。采用非房室和房室分析方法进行药代动力学和药效学分析。

结果

重复给予依维莫司和 binimetinib 后,bupropion 暴露量未增加,而 rosuvastatin C 和接受者操作特性曲线(ROC)下面积(AUC)分别增加约 2.7 倍和 1.6 倍。CP-I 增加很小,表明依维莫司对 rosuvastatin 的主要作用是通过 BCRP。根据其代谢和转运蛋白特征对他汀类药物进行分类表明,pravastatin 与依维莫司联合使用时相互作用的潜力最小。

结论

这些临床研究的结果表明,依维莫司不会导致临床相关的 CYP2B6 诱导或抑制,但它是 BCRP 的抑制剂,并且可能也会在较小程度上抑制 OATP1B1/3。基于这些结果,可能需要考虑相应地转换他汀类药物或减少他汀类药物的剂量,以与依维莫司联合使用。

临床试验注册

ClinicalTrials.gov NCT03864042,于 2019 年 3 月 6 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5a/11052825/515aadb1dffc/40262_2024_1352_Fig1_HTML.jpg

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