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Oral topotecan: bioavailability and effect of food co-administration
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  • Regular Article
  • Open access
  • Published: 11 June 1999

Oral topotecan: bioavailability and effect of food co-administration

  • V M M Herben1,2,
  • H Rosing1,
  • W W ten Bokkel Huinink2,
  • D M van Zomeren1,
  • D Batchelor2,
  • E Doyle3,
  • F D Beusenberg4,
  • J H Beijnen1,2 &
  • …
  • J H M Schellens2 

British Journal of Cancer volume 80, pages 1380–1386 (1999)Cite this article

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Summary

The aims of the study were twofold: (1) to evaluate the effect of food on the relative oral bioavailability of topotecan gelatin capsules in patients with solid tumours, and (2) to determine the absolute bioavailability of oral topotecan with reference to the intravenous (i.v.) formulation. The study had a randomized two-period cross-over design. On day 1 of the first treatment course patients were administered 2.3 mg m–2 day–1 of oral topotecan with or without a high-fat breakfast. They crossed over to receive the alternate regimen on day 2. In the second course (3 weeks later) fasted patients received topotecan orally (2.3 mg m–2 day–1) or i.v. (1.5 mg m–3 day). They crossed over to receive the alternate regimen on day 2. On days 3–5 of both treatment courses patients received oral topotecan. Plasma pharmacokinetics were performed on days 1 and 2 of the first and second course using a high-performance liquid chromatographic assay. Eighteen patients were enrolled in the study. The ratio of the area under the curve to infinity during fasted and high-fat treatment was 0.93 ± 0.23 (90% confidence interval (CI) 0.83–1.03). Maximal plasma concentrations of topotecan were similar after ingestion of the capsules with (10.6 ± 4.4 ng ml–1) or without food (9.2 ± 4.1 ng ml–1) (P = 0.130). The time needed to reach maximal plasma levels was significantly prolonged after food intake (median 3.1 h, range 2.8–6.1) compared to fasted conditions (2.0 h, range 1.1–8.1) (P = 0.013). The absolute bioavailability of topotecan averaged 42 ± 13% (90% CI 37– 47%). The apparent terminal half-life was significantly longer after administration of oral topotecan (3.9 ± 1.0 h) than after i.v. administration (2.7 ± 0.4 h) (P < 0.001). Topotecan demonstrates suitable bioavailability for oral treatment. Co-administration of the topotecan gelatin capsules with a high-fat breakfast leads to a small decrease in absorption rate but does not affect the extent of absorption.

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. Department of Pharmacy and Pharmacology, Slotervaart Hospital/The Netherlands Cancer Institute, Amsterdam, The Netherlands

    V M M Herben, H Rosing, D M van Zomeren & J H Beijnen

  2. Department of Medical Oncology, Antoni van Leeuwenhoek Hospital/The Netherlands Cancer Institute, Amsterdam, The Netherlands

    V M M Herben, W W ten Bokkel Huinink, D Batchelor, J H Beijnen & J H M Schellens

  3. Department of Drug Metabolism and Pharmacokinetics, SmithKline Beecham Pharmaceuticals, Hertfordshire, UK

    E Doyle

  4. SmithKline Beecham Farma, Rijswijk, The Netherlands

    F D Beusenberg

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Herben, V., Rosing, H., Huinink, W. et al. Oral topotecan: bioavailability and effect of food co-administration. Br J Cancer 80, 1380–1386 (1999). https://doi.org/10.1038/sj.bjc.6690532

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  • Received: 10 June 1998

  • Revised: 08 December 1998

  • Accepted: 21 January 1999

  • Published: 11 June 1999

  • Issue date: July 1999

  • DOI: https://doi.org/10.1038/sj.bjc.6690532

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Keywords

  • topotecan
  • oral
  • bioavailability
  • food

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