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高血压与血管内皮生长因子(VEGF)受体酪氨酸激酶抑制:对肾功能的影响。

Hypertension and VEGF (Vascular Endothelial Growth Factor) Receptor Tyrosine Kinase Inhibition: Effects on Renal Function.

作者信息

Boursiquot Brian C, Zabor Emily C, Glezerman Ilya G, Jaimes Edgar A

机构信息

From the Stanford University School of Medicine, CA (B.C.B.); Department of Epidemiology & Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY (E.C.Z.); Department of Medicine, Division of Nephrology & Hypertension, Weill-Cornell Medical College, New York, NY (I.G.G., E.A.J.); and Department of Medicine, Renal Service, Memorial Sloan Kettering Cancer Center, New York, NY (I.G.G., E.A.J.).

出版信息

Hypertension. 2017 Jul 24. doi: 10.1161/HYPERTENSIONAHA.117.09275.

DOI:10.1161/HYPERTENSIONAHA.117.09275
PMID:28739979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5783791/
Abstract

VEGF (vascular endothelial growth factor) receptor tyrosine kinase inhibitors have become first-line therapy for metastatic renal cell carcinoma. Their use commonly leads to hypertension, but their effects on long-term renal function are not known. In addition, it has been suggested that the development of hypertension is linked to treatment efficacy. The objective of this study was to determine the effects of these drugs on long-term renal function, especially in those with renal dysfunction at baseline, and to examine the role of hypertension on these effects. Serum creatinine measurements were used to calculate the estimated glomerular filtration rate for 130 renal cell carcinoma patients who were treated with this class of tyrosine kinase inhibitors. New or worsening hypertension was defined by documented start or addition of antihypertensive medications. Overall, the use of tyrosine kinase inhibitors in patients with estimated glomerular filtration <60 or ≥60 mL/min per 1.73 m was not associated with a decline in long-term renal function. During follow-up, 41 patients developed new or worsening hypertension within 30 days from first drug administration, and this was not linked to further reductions in glomerular filtration. These patients seemed to survive longer than those who did not develop hypertension within 30 days, although this was not statistically significant (=0.07). Our findings suggest that the use of VEGF tyrosine kinase inhibitors does not adversely affect long-term renal function even in the setting of new-onset hypertension or reduced renal function at baseline.

摘要

血管内皮生长因子(VEGF)受体酪氨酸激酶抑制剂已成为转移性肾细胞癌的一线治疗方法。其使用通常会导致高血压,但其对长期肾功能的影响尚不清楚。此外,有人认为高血压的发生与治疗效果有关。本研究的目的是确定这些药物对长期肾功能的影响,特别是对基线时存在肾功能不全的患者,并探讨高血压在这些影响中的作用。对130例接受此类酪氨酸激酶抑制剂治疗的肾细胞癌患者,通过血清肌酐测量来计算估计肾小球滤过率。新发或恶化的高血压定义为有记录的开始使用或加用抗高血压药物。总体而言,估计肾小球滤过率<60或≥60ml/(min·1.73m²)的患者使用酪氨酸激酶抑制剂与长期肾功能下降无关。在随访期间,41例患者在首次给药后30天内出现新发或恶化的高血压,这与肾小球滤过率的进一步降低无关。这些患者似乎比那些在30天内未发生高血压的患者存活时间更长,尽管这在统计学上无显著差异(P=0.07)。我们的研究结果表明,即使在新发高血压或基线肾功能降低的情况下,使用VEGF酪氨酸激酶抑制剂也不会对长期肾功能产生不利影响。