Hypertension and overall survival in metastatic colorectal cancer patients treated with bevacizumab-containing chemotherapy

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Abstract

Background:Hypertension (HTN) is a common toxicity of anti-VEGF (vascular endothelial growth factor) antibody treatment. It may be a marker of VEGF signalling pathway inhibition and therefore represent a cancer biomarker in metastatic colorectal cancer (mCRC) patients treated with chemotherapy and bevacizumab.Methods:A total of 101 consecutive patients with mCRC were treated with standard chemotherapy combined with bevacizumab at dose of 2.5 mg kg 1 per week in a single centre. The median follow-up time of the patients alive was 64 months. Blood pressure was measured before each bevacizumab infusion, and HTN was graded according to common toxicity criteria for adverse events version 3.0.Results:Overall, 57 patients (56%) developed grade 1 HTN (median blood pressure 168/97 mm Hg), whereas 44 (44%) remained normotensive when treated with bevacizumab-containing chemotherapy regimen. Overall response rate was higher among patients with HTN (30 vs 20%; P0.025). Hypertension was associated with improved progression-free survival (10.5 vs 5.3 months; P0.008) and overall survival (25.8 vs 11.7 months; P0.001), and development of HTN within 3 months had an independent, prognostic influence in a multivariate landmark survival analysis together with other known mCRC prognostic factors (P0.007). There was no association between HTN and development of thromboembolic complications.Conclusion:Hypertension may predict outcome of bevacizumab-containing chemotherapy in mCRC. These data require confirmation in prospective studies including pharmacodynamic and pharmacokinetic analyses. © 2011 Cancer Research UK. All rights reserved.

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Österlund, P., Soveri, L. M., Isoniemi, H., Poussa, T., Alanko, T., & Bono, P. (2011). Hypertension and overall survival in metastatic colorectal cancer patients treated with bevacizumab-containing chemotherapy. British Journal of Cancer, 104(4), 599–604. https://doi.org/10.1038/bjc.2011.2

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