Literature DB >> 11221957

The platelet-sparing effect of paclitaxel is not related to changes in the pharmacokinetics of carboplatin.

K Fujiwara1, H Yamauchi, S Suzuki, H Ishikawa, Y Tanaka, M Fujiwara, I Kohno.   

Abstract

PURPOSE: To determine whether the platelet-sparing effect of paclitaxel is related to changes in pharmacology of carboplatin.
METHODS: A group of 32 patients with epithelial ovarian cancer were treated with intraperitoneal (i.p.) carboplatin-based chemotherapy with carboplatin alone or in combination with cyclophosphamide or paclitaxel, and the relationship between the pharmacology of serum platinum and thrombocytopenia was examined. The target AUC of i.p. carboplatin was 6.5 mg min/ml. Cyclophosphamide was administered intravenously at 400 mg/m2 after i.p. carboplatin and paclitaxel at 175 mg/m2 was given before i.p. carboplatin.
RESULTS: Ten patients received i.p. carboplatin alone, 10 received cyclophosphamide and 12 received paclitaxel. The ages of the patients, body surface area, serum creatinine, platelet count before chemotherapy, and the total dose of carboplatin in each patient were similar in all groups. The measured AUC, Cmax, T 1/2, and MRT were similar in these groups. The nadir platelet counts were significantly higher (P = 0.0018) in patients treated with i.p. carboplatin with paclitaxel (12.1 +/- 4.3 x 10(4)/mm3) compared with carboplatin alone (5.2 +/- 3.3 x 10(4)/mm3) or with cyclophosphamide (5.2 +/- 4.8 x 10(4)/mm3). The percentage decrease in platelet counts was significantly lower (62.5 +/- 18.2%) in patients treated with paclitaxel than in the other two groups (81.5 +/- 12.6% carboplatin alone, 88.7 +/- 7.9% with cyclophosphamide).
CONCLUSION: The addition of paclitaxel or cyclophosphamide to i.p. carboplatin did not alter the pharmacology of serum platinum. Thrombocytopenia was significantly less in patients treated with carboplatin in combination with paclitaxel. The platelet-sparing effect of paclitaxel is not related to changes in the pharmacology of carboplatin.

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Year:  2001        PMID: 11221957     DOI: 10.1007/s002800000212

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  5 in total

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Journal:  Int J Cancer       Date:  2011-03-04       Impact factor: 7.396

2.  Analysis of the cytotoxic activity of carboplatin and gemcitabine combination.

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3.  Paclitaxel Enhances Carboplatin-DNA Adduct Formation and Cytotoxicity.

Authors:  Shuai Jiang; Amy W Pan; Tzu-yin Lin; Hongyong Zhang; Michael Malfatti; Kenneth Turteltaub; Paul T Henderson; Chong-xian Pan
Journal:  Chem Res Toxicol       Date:  2015-11-11       Impact factor: 3.739

4.  Modelling chemotherapy effects on granulopoiesis.

Authors:  Sibylle Schirm; Christoph Engel; Markus Loeffler; Markus Scholz
Journal:  BMC Syst Biol       Date:  2014-12-24

5.  Molecular Dissection of Induced Platinum Resistance through Functional and Gene Expression Analysis in a Cell Culture Model of Bladder Cancer.

Authors:  Sisi Wang; Hongyong Zhang; Tiffany M Scharadin; Maike Zimmermann; Bin Hu; Amy Wang Pan; Ruth Vinall; Tzu-yin Lin; George Cimino; Patrick Chain; Momchilo Vuyisich; Cheryl Gleasner; Kim Mcmurry; Michael Malfatti; Kenneth Turteltaub; Ralph de Vere White; Chong-xian Pan; Paul T Henderson
Journal:  PLoS One       Date:  2016-01-22       Impact factor: 3.240

  5 in total

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