Authors
K Agergaard, M Mau‐Sørensen, T Bjerregaard Stage, TL Jørgensen, RE Hassel, Karina Dahl Steffensen, JW Pedersen, Marie Louise Holm Milo, SH Poulsen, Anton Pottegård, J Hallas, K Brøsen, TK Bergmann
Publication date
2017/9
Journal
Clinical Pharmacology & Therapeutics
Volume
102
Issue
3
Pages
547-553
Description
Paclitaxel is mainly eliminated by CYP2C8 in the liver. CYP2C8 is strongly inhibited by the clopidogrel metabolite acyl‐β‐D‐glucuronide. To determine if this interaction has clinical relevance, we identified 48 patients treated with clopidogrel and paclitaxel using databases and a prescription register. Peripheral sensory neuropathy was retrospectively evaluated from medical charts and compared to that of 88 age‐ and sex‐matched controls treated with paclitaxel and low‐dose aspirin. By a cumulative dose of 1,500 mg paclitaxel, 35% of the patients had developed severe neuropathy. The overall hazard ratio between clopidogrel use and severe paclitaxel neuropathy was 1.7 (95% confidence interval, 0.9–3.0). Among those receiving a high‐dose paclitaxel regimen, the hazard ratio was 2.3 (95% confidence interval, 1.1–4.5). Our study indicates that clopidogrel is associated with a clinically relevant increased risk of …
Total citations
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Scholar articles
K Agergaard, M Mau‐Sørensen, TB Stage… - Clinical Pharmacology & Therapeutics, 2017