Literature DB >> 11496337

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

R Kim1, A Osaki, T Toge.   

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/m(2) to 80 mg/m(2) 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/m(2), 3 cases of 60 mg/m(2) and 4 cases of 80 mg/m(2) 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/m(2), 60 mg/m(2) and 80 mg/m(2) in the weekly paclitaxel was 1.94, 2.18 and 1.54 microM, 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.

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Year:  2001        PMID: 11496337     DOI: 10.3892/or.8.5.1171

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  5 in total

1.  Phase II study of weekly paclitaxel by one-hour infusion for advanced gastric cancer.

Authors:  Yasunori Emi; Manabu Yamamoto; Ikuo Takahashi; Hiroyuki Orita; Yoshihiro Kakeji; Shunji Kohnoe; Yoshihiko Maehara
Journal:  Surg Today       Date:  2008-10-29       Impact factor: 2.549

2.  Pharmacokinetics of paclitaxel in a hemodialysis patient with advanced gastric cancer: A case report.

Authors:  Susumu Kawate; Izumi Takeyoshi; Yasuo Morishita
Journal:  World J Gastroenterol       Date:  2006-08-28       Impact factor: 5.742

3.  A Phase II Study of S-1 Monotherapy as a First-line Combination Therapy of S-1 Plus Cisplatin as a Second-line Therapy, and Weekly Paclitaxel Monotherapy as a Third-line Therapy in Patients with Advanced Gastric Carcinoma: A Second Report.

Authors:  Yasushi Rino; Norio Yukawa; Hitoshi Murakami; Nobuyuki Wada; Roppei Yamada; Tsutomu Hayashi; Tsutomu Sato; Takashi Ohshima; Munetaka Masuda; Toshio Imada
Journal:  Clin Med Insights Oncol       Date:  2010-03-24

4.  Phase II Study of S-1 Monotherapy as a First-line, Combination Therapy of S-1 plus Cisplatin as a Second-line, and Weekly Paclitaxel Monotherapy as a Third-line Therapy in Patients with Advanced Gastric Carcinoma: Phase II Study of S-1, S-1 plus Cisplatin, and Weekly Paclitaxel in Patients with Advanced Gastric Carcinoma.

Authors:  Yasushi Rino; Norio Yukawa; Nobuyuki Wada; Makoto Suzuki; Hitoshi Murakami; Takanobu Yamada; Hirotaka Nakayama; Naoto Yamamoto; Tsutomu Sato; Roppei Yamada; Takashi Ohshima; Munetaka Masuda; Toshio Imada
Journal:  Clin Med Oncol       Date:  2008-04-28

5.  Lapatinib-induced annexin A6 upregulation as an adaptive response of triple-negative breast cancer cells to EGFR tyrosine kinase inhibitors.

Authors:  Sarrah E Widatalla; Olga Y Korolkova; Diva S Whalen; J Shawn Goodwin; Kevin P Williams; Josiah Ochieng; Amos M Sakwe
Journal:  Carcinogenesis       Date:  2019-08-22       Impact factor: 4.944

  5 in total

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