Hypertension as predictor of sunitinib treatment outcome in metastatic renal cell carcinoma

Acta Oncol. 2011 May;50(4):569-73. doi: 10.3109/0284186X.2010.543696. Epub 2011 Jan 5.

Abstract

Hypertension and hypothyreoidism are frequent side effects of VEGFR-inhibitors. We investigated whether hypertension or hypothyreoidism diagnosed during sunitinib treatment is associated with treatment efficacy.

Material and methods: Sixty-four consecutive patients with metastatic renal cell cancer (RCC) were treated with sunitinib in a single center. Hypertension was defined as persistent blood pressure >150/100 mmHg or blood pressure requiring intensification of pre-existing anti-hypertensive medication. Hypothyreoidism was defined as elevation of TSH levels and clinical symptoms requiring hormone replacement therapy (≥Gr. II hypothyreoidim).

Results: Twenty-four (38%) patients developed hypertension and 12 (19%) hypothyreoidism. The dose of sunitinib administered was not significantly associated with hypertension or hypothyreoidism. There was no correlation between hypertension and hypothyreoidism. Hypertension was associated with frequent tumor response to sunitinib, a long time to disease progression and long overall survival (p= 0.001, 0.0003 and 0.001, respectively). In a multivariate analysis, hypertension was an independent predictor of progression-free survival (hazard ratio, 0.21; 95% CI 0.076 to 0.59, p=0.0030). There were no statistically significant differences in the frequency of ≥ grade 3 adverse events between patients with or without hypertension.

Conclusion: Sunitinib-associated hypertension may be a strong predictive marker for treatment efficacy in metastatic RCC.

MeSH terms

  • Adenocarcinoma, Clear Cell / drug therapy*
  • Adult
  • Aged
  • Aged, 80 and over
  • Angiogenesis Inhibitors / adverse effects*
  • Female
  • Humans
  • Hypertension / chemically induced*
  • Indoles / adverse effects*
  • Kidney Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Neoplasm Staging
  • Prognosis
  • Pyrroles / adverse effects*
  • Risk Factors
  • Sunitinib

Substances

  • Angiogenesis Inhibitors
  • Indoles
  • Pyrroles
  • Sunitinib