Treatment of bevacizumab-induced hypertension by amlodipine

被引:0
|
作者
Olivier Mir
Romain Coriat
Stanislas Ropert
Laure Cabanes
Benoit Blanchet
Sandra Camps
Bertrand Billemont
Bertrand Knebelmann
François Goldwasser
机构
[1] Paris Descartes University,CERIA (Centre for Research on Angiogenesis Inhibitors), Department of Medical Oncology, Cochin Teaching Hospital, AP
[2] Paris Descartes University,HP
[3] Paris Descartes University,Department of Cardiology, Cochin Teaching Hospital, AP
[4] Paris Descartes University,HP
来源
Investigational New Drugs | 2012年 / 30卷
关键词
Hypertension; Bevacizumab; Amlodipine; Dose intensity; VEGF;
D O I
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学科分类号
摘要
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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页码:702 / 707
页数:5
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