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DOI 10.1016/j.urolonc.2009.07.023

Медицинская библиотека · Urologic oncology · 2009

Evolution of renal function in patients treated with antiangiogenics after nephrectomy for renal cell carcinoma.

Launay-Vacher Vincent, Ayllon Jorge, Janus Nicolas, Medioni Jacques, Deray Gilbert, Isnard-Bagnis Corinne, Oudard Stéphane

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Аннотация

PURPOSE: Side effects of antiangiogenic agents are moderate compared with other therapies. The most frequent adverse events are of a renovascular origin and manifest as hypertension (HTN) and thrombotic microangiopathy. To date, data are scanty on the renal tolerance of such drugs regarding renal function as itself, i.e., glomerular filtration rate (GFR). We report on the evolution of GFR in patients receiving antiangiogenic therapy after unilateral nephrectomy for kidney cancer.

PATIENTS AND

METHODS

Data from 73 patients followed in our oncology department for kidney cancer, who had undergone unilateral nephrectomy, and received any antiangiogenic therapy were reviewed. Their GFR was calculated using the aMDRD formula.

RESULTS

All patients showed a declining renal function over time (-1.23 and -2.51 mL/min/1.73 m(2) using the slope of the curve or the difference between GFR at baseline and that at the end of treatment, respectively). Among them, patients who were recorded as having HTN before initiation of antiangiogenic therapy showed a higher decrease in their GFR of -13.28 and -12.06 mL/min/1.73 m(2).

CONCLUSION

We recommend that blood pressure should be measured closely in those patients before initiation of antiangiogenic therapy. When HTN is diagnosed, it should be treated and renal function should be monitored since those patients may be at risk for rapidly decreasing renal function under therapy.

Для цитирования: Launay-Vacher Vincent, Ayllon Jorge, Janus Nicolas, Medioni Jacques, Deray Gilbert, Isnard-Bagnis Corinne, Oudard Stéphane. Evolution of renal function in patients treated with antiangiogenics after nephrectomy for renal cell carcinoma.. Urologic oncology. 2009. DOI: 10.1016/j.urolonc.2009.07.023.

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