Impact of hyponatremia on survival of patients with metastatic renal cell carcinoma treated with molecular targeted therapy

Abstract

Objectives: Hyponatremia is reported to be associated with poor survival in localized renal cell carcinoma and metastatic renal cell carcinoma treated with immunotherapy. However, there are no reports on the relationship between hyponatremia and prognosis of metastatic renal cell carcinoma treated with molecular targeted therapy. We evaluated the prognostic significance of hyponatremia in metastatic renal cell carcinoma treated with molecular targeted therapy as first-line therapy. Methods: We retrospectively analyzed a database comprising 87 patients treated from April 2008 to July 2011 with sorafenib or sunitinib as first-line therapy for metastatic renal cell carcinoma. Patients were divided into three groups according to serum sodium level: severe hyponatremia (≤134mEq/L), mild hyponatremia (135-137mEq/L) and normal natremia (≥138mEq/L). Results: Median cancer-specific survival time was 8.8months in the patients with severe and mild hyponatremia, and 32.6months in the patients with normal natremia (P<0.001). Multivariate analysis showed severe and mild hyponatremia to be significantly associated with cancer-specific survival (hazard ratio 6.228; 95% confidence interval 2.161-17.947, P=0.001; hazard ratio 3.374; 95% confidence interval 1.294-8.798, P=0.013), respectively. Neutrophilia and high C-reactive protein level (C-reactive protein ≥1.0mg/dL) were significant prognostic factors to predict inferior cancer-specific survival. In Harrell's concordance index calculation, hyponatremia could significantly improve the predictive accuracy for estimation of survival probability (P=0.028). Conclusions: Hyponatremia (<138mEq/L), neutrophilia and high C-reactive protein levels seem to represent significant predictive factors for cancer-specific survival in metastatic renal cell carcinoma patients treated with molecular targeted therapy as first line therapy. Furthermore, hyponatremia might be significantly associated with chronic inflammation and tumor aggressiveness. © 2012 The Japanese Urological Association.