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所有抗血管内皮生长因子药物均可诱发“子痫前期样综合征”:一项罕见病例研究。

All anti-vascular endothelial growth factor drugs can induce 'pre-eclampsia-like syndrome': a RARe study.

作者信息

Vigneau Cécile, Lorcy Nolwenn, Dolley-Hitze Thibault, Jouan Florence, Arlot-Bonnemains Yannick, Laguerre Brigitte, Verhoest Gregory, Goujon Jean Michel, Belaud-Rotureau Marc-Antoine, Rioux-Leclercq Nathalie

机构信息

CHU Rennes, Service de Néphrologie, Rennes, France.

出版信息

Nephrol Dial Transplant. 2014 Feb;29(2):325-32. doi: 10.1093/ndt/gft465. Epub 2013 Dec 2.

Abstract

BACKGROUND

Specific therapies that target vascular endothelial growth factor (VEGF) and its receptors have improved the survival of patients with metastatic cancers, but can induce side effects. Renal side effects (proteinuria, hypertension and renal failure) are underestimated.

METHODS

The French RARe (Reins sous traitement Anti-VEGF Registre) study collects data on patients with cancer who had a renal biopsy because of major renal side effects during treatment with anti-VEGF drugs.

RESULTS

We collected 22 renal biopsies performed 16.2±10.6 months after the beginning of treatment; of which 21 had hypertension, mean proteinuria was 2.97±2.00 g/day and mean serum creatinine, 134±117 µmol/L. Thrombotic microangiopathy (TMA) was observed in 21 biopsy specimens, sometimes associated with acute tubular necrosis (ATN; n=4). TMA histological lesions were more important than the biological signs of TMA could suggest. Patients with ATN of >20% had higher serum creatinine levels than those with only TMA (231 versus 95 µmol/L). Nephrin, podocin and synaptopodin were variably down-regulated in all renal biopsies. VEGF was down-regulated in all glomeruli.

CONCLUSION

This study underlines the importance of regular clinical and biological cardiovascular and renal checking during all anti-VEGF therapies for cancer for early detection of renal dysfunction. Collaboration between oncologists and nephrologists is essential. In such cases, renal biopsy might help in appreciating the severity of the renal lesions and after multidisciplinary discussion whether or not it is safe to continue the treatment.

摘要

背景

针对血管内皮生长因子(VEGF)及其受体的特异性疗法提高了转移性癌症患者的生存率,但会引发副作用。肾脏副作用(蛋白尿、高血压和肾衰竭)被低估了。

方法

法国RARe(抗VEGF治疗中的肾脏登记)研究收集了因在接受抗VEGF药物治疗期间出现严重肾脏副作用而进行肾活检的癌症患者的数据。

结果

我们收集了22例在治疗开始后16.2±10.6个月进行的肾活检;其中21例有高血压,平均蛋白尿为2.97±2.00 g/天,平均血清肌酐为134±117 µmol/L。在21个活检标本中观察到血栓性微血管病(TMA),有时与急性肾小管坏死(ATN;n = 4)相关。TMA的组织学病变比TMA的生物学体征所提示的更严重。ATN > 20%的患者血清肌酐水平高于仅患有TMA的患者(231对95 µmol/L)。在所有肾活检中,nephrin、podocin和synaptopodin均有不同程度的下调。VEGF在所有肾小球中均下调。

结论

本研究强调了在所有癌症抗VEGF治疗期间进行定期临床和生物学心血管及肾脏检查以早期发现肾功能障碍的重要性。肿瘤学家和肾病学家之间的合作至关重要。在这种情况下,肾活检可能有助于评估肾脏病变的严重程度,并在多学科讨论后确定继续治疗是否安全。

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