Pharmacokinetic study of weekly administration dose of paclitaxel in patients with advanced or recurrent gastric cancer in Japan

被引:49
作者
Kobayashi, Michiya [1 ]
Oba, Koji [2 ]
Sakamoto, Junichi [3 ]
Kondo, Ken [4 ]
Nagata, Naoki [5 ]
Okabayashi, Takehiro [6 ]
Namikawa, Tsutomu [6 ]
Hanazaki, Kazuhiro [6 ]
机构
[1] Kochi Med Sch, Dept Human Hlth & Med Sci, Nankoku, Kochi 7838505, Japan
[2] Kyoto Univ, Dept Epidemiol & Clin Res Informat Management, Kyoto, Japan
[3] Nagoya Univ, Grad Sch Med, Young Leaders Program, Nagoya, Aichi 4648601, Japan
[4] Nagoya Natl Hosp, Dept Surg, Nagoya, Aichi, Japan
[5] Univ Occupat & Environm Hlth, Dept Surg 1, Kitakyushu, Fukuoka 807, Japan
[6] Kochi Med Sch, Dept Surg, Nankoku, Kochi, Japan
关键词
paclitaxel; chemotherapy; gastric cancer; pharmacokinetic study; advanced gastric cancer;
D O I
10.1007/s10120-006-0411-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background. We aimed to clarify the relationship between the maximum tolerated dose and plasma concentration of paclitaxel in Japanese patients with gastric cancer on a weekly paclitaxel administration regimen. Methods. Thirty-three patients with advanced or recurrent gastric cancer were treated with escalating doses of paclitaxel, administered weekly, along with a fixed dose of 5-fluorouracil or cisplatin. Results. The plasma concentration of paclitaxel remained above 8.5 ng/ml for 24 h after administration. The mean area under the curve increased significantly with escalating dosage levels (R = 0.63; P < 0.001). At level 4, patients showing dose-limiting toxicity had a significantly higher plasma paclitaxel concentration than patients without it. Conclusion. The weekly administration of paclitaxel, for which a single dose is about one-third of the dose for a triweekly treatment regimen, is clinically feasible and appropriate in terms of toxicity and the maintenance of an effective plasma concentration.
引用
收藏
页码:52 / 57
页数:6
相关论文
共 28 条
[1]
Chang YF, 1996, CANCER, V77, P14, DOI 10.1002/(SICI)1097-0142(19960101)77:1<14::AID-CNCR4>3.0.CO
[2]
2-N
[3]
Phase I and pharmacologic study of paclitaxel administered weekly in patients with relapsed ovarian cancer [J].
Fennelly, D ;
Aghajanian, C ;
Shapiro, F ;
OFlaherty, C ;
McKenzie, M ;
OConnor, C ;
Tong, W ;
Norton, L ;
Spriggs, D .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) :187-192
[4]
Phase II trial of outpatient schedule of paclitaxel in patients with previously untreated metastatic, measurable adenocarcinoma of the stomach [J].
Garcia, AA ;
Leichman, CG ;
Lenz, HJ ;
Baranda, J ;
Lujan, R ;
Casagrande, Y ;
Leichman, L .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2001, 31 (06) :275-278
[5]
Glantz MJ, 1996, SEMIN ONCOL, V23, P128
[6]
Schedule-dependent interaction between paclitaxel and 5-fluorouracil in human carcinoma cell lines in vitro [J].
Kano, Y ;
Akutsu, M ;
Tsunoda, S ;
Ando, J ;
Matsui, J ;
Suzuki, K ;
Ikeda, T ;
Inoue, Y ;
Adachi, KI .
BRITISH JOURNAL OF CANCER, 1996, 74 (05) :704-710
[7]
Kim YH, 1999, CANCER, V85, P295, DOI 10.1002/(SICI)1097-0142(19990115)85:2<295::AID-CNCR5>3.0.CO
[8]
2-H
[9]
Phase I study with a weekly 1 h infusion of paclitaxel in heavily pretreated patients with metastatic breast and ovarian cancer [J].
Klaassen, U ;
Wilke, H ;
Strumberg, D ;
Eberhardt, W ;
Korn, M ;
Seeber, S .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (03) :547-549
[10]
A phase II study of paclitaxel, weekly, 24-hour continuous infusion 5-fluorouracil, folinic acid and cisplatin in patients with advanced gastric cancer [J].
Kollmannsberger, C. ;
Quietzsch, D. ;
Haag, C. ;
Lingenfelsers, T. ;
Schroeder, M. ;
Hartmann, J. T. ;
Baronius, W. ;
Hempel, V. ;
Clemens, M. ;
Kanz, L. ;
Bokemeyer, C. .
BRITISH JOURNAL OF CANCER, 2000, 83 (04) :458-462