TY - JOUR
T1 - All anti-vascular endothelial growth factor drugs can induce 'pre-eclampsia-like syndrome'
T2 - A RARe study
AU - Vigneau, Cécile
AU - Lorcy, Nolwenn
AU - Dolley-Hitze, Thibault
AU - Jouan, Florence
AU - Arlot-Bonnemains, Yannick
AU - Laguerre, Brigitte
AU - Verhoest, Gregory
AU - Goujon, Jean Michel
AU - Belaud-Rotureau, Marc Antoine
AU - Rioux-Leclercq, Nathalie
N1 - Funding Information:
Sylvie Le Stum for database, N. Quellard and B. Fernandez from Electron Microscopy Unit, Hospital, Poitiers, France and Elisabetta Andermarcher for English revision. This work was supported by Région Bretagne, Université Rennes 1 (CoREC/ Cs scientifique).
PY - 2014/2
Y1 - 2014/2
N2 - 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.ConclusionThis 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.
AB - 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.ConclusionThis 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.
KW - anti-VEGF
KW - drug side effects
KW - kidney biopsy
KW - pre-eclampsia
UR - https://www.scopus.com/pages/publications/84896739805
U2 - 10.1093/ndt/gft465
DO - 10.1093/ndt/gft465
M3 - Article
SN - 0931-0509
VL - 29
SP - 325
EP - 332
JO - Nephrology Dialysis Transplantation
JF - Nephrology Dialysis Transplantation
IS - 2
ER -