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吉非替尼与/不与氯沙坦及选择性5-羟色胺再摄取抑制剂(SSRI)的临床前药物相互作用(DDI):西酞普兰、氟西汀、氟伏沙明、帕罗西汀、舍曲林和文拉法辛。

Pre-clinical drug-drug interactions (DDIs) of gefitinib with/without losartan and selective serotonin reuptake inhibitors (SSRIs): citalopram, fluoxetine, fluvoxamine, paroxetine, sertraline, and venlafaxine.

作者信息

Luong Thu-Lan T, Powers Chelsea N, Reinhardt Brian J, Weina Peter J

机构信息

Walter Reed National Military Medical Center, Biomedical Laboratory, Department of Research, Bethesda, MD, 8901 Rockville Pike, Bethesda, MD, 20889, United States.

Defense Health Headquarters, 7700 Arlington Blvd, Falls Church, VA, 22042, United States.

出版信息

Curr Res Pharmacol Drug Discov. 2022 Jun 14;3:100112. doi: 10.1016/j.crphar.2022.100112. eCollection 2022.

Abstract

OBJECTIVE

To evaluate drug-drug interactions (DDIs) between gefitinib with/without losartan and selective serotonin reuptake inhibitors (SSRIs).

METHODS

supersomes were used to identify CYP isoenzymes (CYP1A2, 2C9, 2C19, 2D6, and 3A4) involved in drug metabolism, and pooled cryopreserved primary human hepatocytes were employed to investigate DDIs.

RESULTS

The isoenzymes that showed drug degradation are listed in parentheses beside the respective drug: gefitinib (CYP2D6, 3A4, 1A2, 2C9, and 2C19), losartan (CYP2C9 and 3A4), citalopram (CYP2D6, 2C19, 3A4, and 2C9), fluoxetine (CYP2D6, 2C9, and 2C19), fluvoxamine (CYP2D6, 2C9, and 2C19), paroxetine (CYP2D6, 3A4, and 2C9), sertraline (CYP2D6, 2C9, 2C19, 1A2, and 3A4), and venlafaxine (CYP2D6 and 2C19).DDIs from human hepatocytes assays revealed that gefitinib had significant metabolic changes in (1:1) combination with paroxetine or sertraline (p-value ​= ​0.042 and 0.025 respectively) and (1:1:1) combination with losartan and fluoxetine, fluvoxamine, paroxetine, or sertraline (p-value ​= ​0.009, 0.027, 0.048, and 0.037 respectively). Losartan showed significant changes in (1:1:1) combination with gefitinib and fluoxetine or sertraline (p-value ​= ​0.026 and 0.008 respectively). Fluoxetine, fluvoxamine, and paroxetine underwent significant changes in (1:1:1) combination with gefitinib and losartan (p-value ​= ​0.003, 0.022, and 0.046 respectively). Sertraline had significant changes within all combinations: DDIs with gefitinib alone and in combination with gefitinib and losartan (p-value ​= ​0.009 and 0.008 respectively). Citalopram and venlafaxine appeared to be unaffected by any combination.

CONCLUSION

The study provides a clear proof-of concept for metabolic DDI testing. While identifying compounds by their inhibition potential can help better predict their metabolism, it cannot resolve problems that arise from DDIs since the overall degree of effectiveness is unknown. As shown in this study, gefitinib has been identified as a weak CYP2C19 and 2D6 inhibitor, however, gefitinib can have significant DDIs with sertraline. Furthermore, multiple drug combinations (1:1:1) can change the significance of previously determined DDIs in (1:1) combination. Thus, assays can potentially provide better guidance for multidrug regimens with minimal risk for DDIs.

摘要

目的

评估吉非替尼与或不与氯沙坦联用与选择性5-羟色胺再摄取抑制剂(SSRI)之间的药物相互作用(DDI)。

方法

使用超微粒体鉴定参与药物代谢的细胞色素P450同工酶(CYP1A2、2C9、2C19、2D6和3A4),并采用冻存的人原代肝细胞池研究药物相互作用。

结果

显示有药物降解的同工酶列于相应药物旁边的括号内:吉非替尼(CYP2D6、3A4、1A2、2C9和2C19)、氯沙坦(CYP2C9和3A4)、西酞普兰(CYP2D6、2C19、3A4和2C9)、氟西汀(CYP2D6、2C9和2C19)、氟伏沙明(CYP2D6、2C9和2C19)、帕罗西汀(CYP2D6、3A4和2C9)、舍曲林(CYP2D6、2C9、2C19、1A2和3A4)和文拉法辛(CYP2D6和2C19)。人肝细胞试验的药物相互作用显示,吉非替尼与帕罗西汀或舍曲林以(1:1)组合时(p值分别为0.042和0.025)以及与氯沙坦和氟西汀、氟伏沙明、帕罗西汀或舍曲林以(1:1:1)组合时(p值分别为0.009、0.027、0.048和0.037)有显著的代谢变化。氯沙坦与吉非替尼和氟西汀或舍曲林以(1:1:1)组合时(p值分别为0.026和0.008)有显著变化。氟西汀、氟伏沙明和帕罗西汀与吉非替尼和氯沙坦以(1:1:1)组合时(p值分别为0.003、0.022和0.046)有显著变化。舍曲林在所有组合中均有显著变化:单独与吉非替尼以及与吉非替尼和氯沙坦组合时的药物相互作用(p值分别为0.009和0.008)。西酞普兰和文拉法辛似乎不受任何组合的影响。

结论

该研究为代谢性药物相互作用检测提供了明确的概念验证。虽然通过抑制潜力鉴定化合物有助于更好地预测其代谢,但由于总体有效性程度未知,无法解决药物相互作用产生的问题。如本研究所示,吉非替尼已被鉴定为一种弱CYP2C19和2D6抑制剂,然而,吉非替尼与舍曲林可能有显著的药物相互作用。此外,多种药物组合(1:1:1)可改变先前确定的(1:1)组合中药物相互作用的显著性。因此,试验可能为药物相互作用风险最小的多药治疗方案提供更好的指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9218239/feb0b18facd7/ga1.jpg

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