索拉非尼继发的心血管和代谢毒性

IF 1.2 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
R. Roa-Chamorro , L. Torres-Quintero , P. González-Bustos
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引用次数: 1

摘要

酪氨酸激酶抑制剂是一类化疗药物,用于许多实体瘤和血液肿瘤的一线和二线治疗。它的毒性相对较低,因为其作用机制是基于对一些参与肿瘤细胞爆炸的酪氨酸激酶的抑制。然而,这种封锁不是选择性的,因此会产生次要影响。索拉非尼可引起动脉高压、甲状腺疾病、腹痛或高淀粉酶血症等。我们必须在治疗期间对这些患者进行监测,以避免副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toxicidad cardiovascular y metabólica secundaria a sorafenib

Tyrosine kinase inhibitors are a family of chemotherapy drugs used in first and second line for many solid and hematological neoplasms. Its toxicity is relatively low, since the mechanism of action is based on the inhibition of some tyrosine kinases involved in the explosion of neoplastic cells. However, this blockade is not selective, so it can produce secondary effects. Sorafenib can produce arterial hypertension, thyroid disorders, abdominal pain or hyperamylasemia, among others. We must monitor these patients during treatment to avoid side effects.

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来源期刊
Hipertension y Riesgo Vascular
Hipertension y Riesgo Vascular Medicine-Internal Medicine
CiteScore
1.70
自引率
16.70%
发文量
38
审稿时长
39 days
期刊介绍: La mejor publicación para mantenerse al día en los avances de la lucha contra esta patología. Incluye artículos de Investigación, Originales, Revisiones, Casos clínicos, Aplicación práctica y Resúmenes comentados a la bibliografía internacional. Además, es la Publicación Oficial de la Sociedad española de Hipertensión-Liga Española para la Lucha contra la Hipertensión Arterial.
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