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Erschienen in: Investigational New Drugs 2/2012

01.04.2012 | PHASE II STUDIES

Treatment of bevacizumab-induced hypertension by amlodipine

verfasst von: Olivier Mir, Romain Coriat, Stanislas Ropert, Laure Cabanes, Benoit Blanchet, Sandra Camps, Bertrand Billemont, Bertrand Knebelmann, François Goldwasser

Erschienen in: Investigational New Drugs | Ausgabe 2/2012

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Summary

Background Hypertension is a common toxicity of anti-VEGF agents, but its optimal treatment remains to define. This study aimed to describe the efficacy and tolerability of amlodipine, a calcium channel blocker, in patients with metastatic malignancies treated with bevacizumab, a humanized monoclonal antibody to VEGF. Patients and methods One hundred and eighty-seven patients with advanced or metastatic NSCLC, colorectal or ovarian cancer receiving bevacizumab (5 mg/kg every 2 weeks or 7.5 mg/kg every 3 weeks) and chemotherapy were eligible for this analysis. Blood pressure was measured at home twice daily according to international guidelines. Patients received amlodipine 5 mg daily for grade ≥2 bevacizumab-induced hypertension. Results Twenty-six patients received amlodipine 5 mg daily for de novo hypertension (group A), and another 10 patients received amlodipine for exacerbation of previously existing hypertension (group B). Hypertension was controlled within 7 days under amlodipine in 23/26 (88.5%, 95%CI: 76.2–100) patients in group A, and 8/10 (80%, 95%CI: 55.2–100) patients in group B, with a favourable toxicity profile. Conclusions Amlodipine 5 mg daily appears safe and efficient for the treatment of hypertension in patients receiving bevacizumab at a dose-intensity of 2.5 mg/kg/week. Further prospective studies are warranted to confirm these results.
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Metadaten
Titel
Treatment of bevacizumab-induced hypertension by amlodipine
verfasst von
Olivier Mir
Romain Coriat
Stanislas Ropert
Laure Cabanes
Benoit Blanchet
Sandra Camps
Bertrand Billemont
Bertrand Knebelmann
François Goldwasser
Publikationsdatum
01.04.2012
Verlag
Springer US
Erschienen in
Investigational New Drugs / Ausgabe 2/2012
Print ISSN: 0167-6997
Elektronische ISSN: 1573-0646
DOI
https://doi.org/10.1007/s10637-010-9549-5

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