A phase I and pharmacokinetic study of the combination of capecitabine and docetaxel in patients with advanced solid tumours
2000

Study of Capecitabine and Docetaxel in Cancer Patients

Sample size: 33 publication Evidence: moderate

Author Information

Author(s): Pronk L C, Vasey P, Sparreboom A, Reigner B, Planting A S Th, Gordon R J, Osterwalder B, Verweij J, Twelves C

Primary Institution: Rotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital, Rotterdam, The Netherlands

Hypothesis

The study aims to determine the maximum tolerated dose and side effects of the combination of capecitabine and docetaxel in patients with advanced solid tumors.

Conclusion

The combination of capecitabine and docetaxel was found to be tolerable with manageable side effects.

Supporting Evidence

  • Thirty-three patients were treated with capecitabine and docetaxel.
  • The dose-limiting toxicity was asthenia grade 2–3.
  • Neutropenia grade 3–4 occurred in 68% of courses.
  • There were two complete responses and three partial responses in tumor responses.

Takeaway

Doctors tested two cancer drugs together to see how much they could give without making patients too sick, and they found a safe amount that worked well.

Methodology

Patients received capecitabine orally and docetaxel intravenously over a specified treatment schedule to assess side effects and maximum tolerated doses.

Digital Object Identifier (DOI)

10.1054/bjoc.2000.1160

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