Pharmacokinetic and biochemical analysis in the treatment of weekly paclitaxel in relapsed breast cancer

  • Authors:
    • Ryungsa Kim
    • Akihiko Osaki
    • Tetsuya Toge
  • View Affiliations

  • Published online on: September 1, 2001     https://doi.org/10.3892/or.8.5.1171
  • Pages: 1171-1176
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

The mechanism(s) by which weekly paclitaxel exerted more therapeutic efficacy than the triweekly schedule in relapsed breast cancer is still unclear. To assess the rationale in therapeutic efficacy of weekly paclitaxel in relapsed breast cancer, pharmacokinetic and biochemical analyses were examined in terms of the mean peak plasma concentration at 0 min (Cmax), 30 min, and 24 h after finishing the infusion, and the extracellular domain of HER-2 in response to the treatment with paclitaxel. Twenty-five patients treated with weekly 1 h infusion of paclitaxel in the dose range from 40 mg/m2 to 80 mg/m2 were studied. Eleven patients responded to the treatment including 4 cases of complete response (CR) and 7 cases of partial response (PR), while 14 patients did not respond including 12 cases of no change (NC) and 2 cases of progressive disease (PD). The plasma concentration of paclitaxel and extracellular domain of HER-2 in the patients were measured by high-pressure liquid chromatography and enzyme immunoassay, respectively. The peak concentration (Cmax) and the other peaks at 30 min and 24 h in 10 patients including 3 cases of 40 mg/m2, 3 cases of 60 mg/m2 and 4 cases of 80 mg/m2 in the weekly paclitaxel were compared in proportion to the increase of dose escalation, and compared to their tumor response. Further, the plasma levels of extracellular domain of HER-2 in 17 patients treated with the weekly paclitaxel were measured, and also compared to their tumor response. The mean Cmax treated with 40 mg/m2, 60 mg/m2 and 80 mg/m2 in the weekly paclitaxel was 1.94, 2.18 and 1.54 μM, respectively. The dose escalation of paclitaxel and the dose intensity were not correlated with the increase of plasma concentration of paclitaxel nor with the tumor response. In contrast, the plasma level of extracellular domain of HER-2 in responders was higher than that of non-responders in the weekly paclitaxel regimen(p=0.0512, Mann-Whitney's U-test). These results suggest that tumor response to the weekly 1 h infusion of paclitaxel was not associated with the plasma concentration and the dose intensity, rather the plasma level of extracellular domain of HER-2 protein may be a predictor of tumor response in the treatment of weekly paclitaxel in relapsed breast cancer.

Related Articles

Journal Cover

September-October 2001
Volume 8 Issue 5

Print ISSN: 1021-335X
Online ISSN:1791-2431

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Kim R, Osaki A and Toge T: Pharmacokinetic and biochemical analysis in the treatment of weekly paclitaxel in relapsed breast cancer. Oncol Rep 8: 1171-1176, 2001
APA
Kim, R., Osaki, A., & Toge, T. (2001). Pharmacokinetic and biochemical analysis in the treatment of weekly paclitaxel in relapsed breast cancer. Oncology Reports, 8, 1171-1176. https://doi.org/10.3892/or.8.5.1171
MLA
Kim, R., Osaki, A., Toge, T."Pharmacokinetic and biochemical analysis in the treatment of weekly paclitaxel in relapsed breast cancer". Oncology Reports 8.5 (2001): 1171-1176.
Chicago
Kim, R., Osaki, A., Toge, T."Pharmacokinetic and biochemical analysis in the treatment of weekly paclitaxel in relapsed breast cancer". Oncology Reports 8, no. 5 (2001): 1171-1176. https://doi.org/10.3892/or.8.5.1171