Division of Nephrology and Dialysis, Istituti Ospitalieri di Cremona, Largo Priori, 1, 26100, Cremona, Italy.
Italian Association of Medical Oncology (AIOM), Milan, Italy.
J Nephrol. 2015 Dec;28(6):647-57. doi: 10.1007/s40620-015-0226-9. Epub 2015 Sep 4.
EGFR and HER2 are found overexpressed and/or activated in many different human malignancies (e.g. breast and colon cancer), and a number of drugs specifically targeting these two tyrosine kinases have been developed over the years as anticancer agents. In the present review, the renal safety profile of presently available agents targeting either HER2 or EGFR will be discussed, together with the peculiarities related to their clinical use in patients with impaired renal function, or even in dialysis. Indeed, even though renal toxicity is not so common with these agents, it may nevertheless happen, especially when these agents are combined with traditional chemotherapeutic agents. As a whole, kidney impairment or dialysis should not be regarded per se as reasons not to administer or to stop an active anti-HER or anti-EGFR anticancer treatment, especially given the possibility of significantly improving the life expectancy of many cancer patients with the use of these agents.
EGFR 和 HER2 在许多不同的人类恶性肿瘤中过度表达和/或激活(例如乳腺癌和结肠癌),多年来,许多专门针对这两种酪氨酸激酶的药物已被开发为抗癌药物。在本综述中,将讨论目前针对 HER2 或 EGFR 的可用药物的肾脏安全性概况,以及它们在肾功能受损甚至透析患者中的临床应用的特点。事实上,尽管这些药物的肾毒性并不常见,但它仍可能发生,尤其是当这些药物与传统化疗药物联合使用时。总的来说,肾脏损害或透析本身不应被视为不给予或停止有效的抗 HER 或抗 EGFR 抗癌治疗的理由,特别是考虑到这些药物的使用有可能显著提高许多癌症患者的预期寿命。