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阿昔替尼可诱发并加重高血压,无论之前是否接受过酪氨酸激酶抑制剂治疗。

Axitinib Induces and Aggravates Hypertension Regardless of Prior Treatment With Tyrosine Kinase Inhibitors.

作者信息

Kadowaki Hiroshi, Ishida Junichi, Akazawa Hiroshi, Yagi Hiroki, Saga-Kamo Akiko, Umei Masahiko, Matsuoka Ryo, Liu Qing, Matsunaga Hiroshi, Maki Hisataka, Sato Yusuke, Kume Haruki, Komuro Issei

机构信息

Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo Tokyo Japan.

Department of Urology, Graduate School of Medicine, The University of Tokyo Tokyo Japan.

出版信息

Circ Rep. 2021 Mar 10;3(4):234-240. doi: 10.1253/circrep.CR-21-0008.

DOI:10.1253/circrep.CR-21-0008
PMID:33842729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8024013/
Abstract

Axitinib is a tyrosine kinase inhibitor (TKI) that inhibits vascular endothelial growth factor receptor signaling and is approved for second-line treatment of advanced renal cell carcinoma (RCC). Although the occurrence of hypertension with axitinib use has been documented, it is unclear whether a first-line TKI regimen can significantly affect the development of hypertension when axitinib is used as second-line therapy. In this single-center retrospective study, advanced RCC patients treated with axitinib after first-line chemotherapy were divided into 2 groups according to the use of TKIs as part of first-line treatment before the initiation of axitinib. Clinical outcomes were compared between patients who were treated with (TKI(+); n=11) or without (TKI(-); n=11) a TKI. Although 63.6% of all patients had hypertension at baseline, axitinib-induced hypertension developed in 81.8% of patients, and 36.4% of patients experienced Grade 3 hypertension. After initiation of axitinib, both systolic and diastolic blood pressures and the hypertension grade were significantly elevated both in the TKI(+) and TKI(-) groups, and the number of antihypertensive drugs was significantly increased among all patients. This study suggests the need for proper monitoring and management of blood pressure in RCC patients treated with axitinib, regardless of a prior regimen with or without TKIs.

摘要

阿昔替尼是一种酪氨酸激酶抑制剂(TKI),可抑制血管内皮生长因子受体信号传导,已被批准用于晚期肾细胞癌(RCC)的二线治疗。虽然使用阿昔替尼时发生高血压的情况已有记录,但尚不清楚当阿昔替尼用作二线治疗时,一线TKI方案是否会显著影响高血压的发生。在这项单中心回顾性研究中,一线化疗后接受阿昔替尼治疗的晚期RCC患者在开始使用阿昔替尼之前,根据是否使用TKI作为一线治疗的一部分分为两组。比较了接受(TKI(+);n = 11)或未接受(TKI(-);n = 11)TKI治疗的患者的临床结局。虽然所有患者中有63.6%在基线时患有高血压,但阿昔替尼诱导的高血压在81.8%的患者中发生,36.4%的患者经历了3级高血压。开始使用阿昔替尼后,TKI(+)组和TKI(-)组的收缩压和舒张压以及高血压分级均显著升高,所有患者中抗高血压药物的数量显著增加。这项研究表明,无论之前是否使用TKI方案,对于接受阿昔替尼治疗的RCC患者,都需要对血压进行适当的监测和管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/86c256d69cd9/circrep-3-234-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/582e7e1c0ead/circrep-3-234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/797c7109b284/circrep-3-234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/5632b89227af/circrep-3-234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/38e33576c64b/circrep-3-234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/86c256d69cd9/circrep-3-234-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/582e7e1c0ead/circrep-3-234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/797c7109b284/circrep-3-234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/5632b89227af/circrep-3-234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/38e33576c64b/circrep-3-234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9514/8024013/86c256d69cd9/circrep-3-234-g005.jpg

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Axitinib in Combination With Toripalimab, a Humanized Immunoglobulin G Monoclonal Antibody Against Programmed Cell Death-1, in Patients With Metastatic Mucosal Melanoma: An Open-Label Phase IB Trial.阿昔替尼联合特泊替尼(一种针对程序性死亡受体-1 的人源化免疫球蛋白 G 单克隆抗体)治疗转移性黏膜黑色素瘤患者的开放标签 Ib 期临床试验。
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