Literature DB >> 9045334

Taxane/platinum/anthracycline combination therapy in advanced epithelial ovarian cancer.

M Hill1, V Macfarlane, J Moore, M E Gore.   

Abstract

A combination of platinum and a taxane is regarded by many as the optimum treatment for advanced epithelial ovarian carcinoma. A recent meta-analysis has suggested that the addition of an anthracycline to platinum-based chemotherapy is associated with a significant survival advantage. We are therefore conducting an ongoing phase I/II study combining drugs from these three classes. We report here the first phase using carboplatin at an area under the concentration-time curve of 7, doxorubicin 50 mg/m2, and paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ) 175 mg/m2 over 3 hours. The treatment was given on a 3-weekly cycle and granulocyte colony-stimulating factor was given if the nadir neutrophil count fell below 0.5 x 10(9)/L and was continued until recovery. Toxicity was assessed according to the Common Toxicity Criteria. All patients were required to have advanced ovarian cancer (stage IC to IV) but be ineligible for standard chemotherapy trials or to have advanced gynecologic malignancy, such as mixed mullerian tumor, fallopian tube carcinoma, coelomic carcinoma, or primary peritoneal carcinoma. To date, seven patients have been treated, and all were of performance status 0 to 2, 18 to 70 years old, with a life expectancy of > or = 3 months. Hematologic toxicity was significant, with all patients having grade 3/4 thrombocytopenia and six of seven grade 3/4 leukopenia. There was, however, only one grade 3/4 infection. Three patients have experienced fatigue, which in two cases was severe, and one patient had grade 3/4 stomatitis. Dose reduction was due to myelosuppression and was required in five patients. Five patients were evaluable for response, all of whom have obtained complete or partial response. There has been no clinical evidence of cardiotoxicity, but four patients had grade 1/2 cardiotoxicity as measured by left ventricular ejection fraction. We conclude that this combination is active and has acceptable but significant toxicity. It is only suitable for very fit patients, and we are currently assessing ways of reducing toxicity.

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Year:  1997        PMID: 9045334

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  6 in total

Review 1.  Dose-intensive approaches to ovarian cancer.

Authors:  N Lambrou; E L Trimble
Journal:  Curr Oncol Rep       Date:  1999-09       Impact factor: 5.075

2.  A dose-finding study of carboplatin-epirubicin-docetaxel in advanced epithelial ovarian cancer.

Authors:  V J O'Neill; S B Kaye; N S Reed; J Paul; J A Davis; P A Vasey
Journal:  Br J Cancer       Date:  2002-05-06       Impact factor: 7.640

3.  A phase I dose-finding study of a combination of pegylated liposomal doxorubicin (Doxil), carboplatin and paclitaxel in ovarian cancer.

Authors:  D D Gibbs; L Pyle; M Allen; M Vaughan; A Webb; S R D Johnston; M E Gore
Journal:  Br J Cancer       Date:  2002-05-06       Impact factor: 7.640

Review 4.  Docetaxel: promising and novel combinations in ovarian cancer.

Authors:  J U Mäenpää
Journal:  Br J Cancer       Date:  2003-12       Impact factor: 7.640

5.  A phase II randomised clinical trial comparing cisplatin, paclitaxel and ifosfamide with cisplatin, paclitaxel and epirubicin in newly diagnosed advanced epithelial ovarian cancer: long-term survival analysis.

Authors:  R Fruscio; N Colombo; A A Lissoni; A Garbi; R Fossati; N Ieda'; V Torri; C Mangioni
Journal:  Br J Cancer       Date:  2008-02-05       Impact factor: 7.640

6.  Docetaxel-carboplatin as first line chemotherapy for epithelial ovarian cancer.

Authors:  P A Vasey; R Atkinson; R Coleman; M Crawford; M Cruickshank; P Eggleton; D Fleming; J Graham; D Parkin; J Paul; N S Reed; S B Kaye
Journal:  Br J Cancer       Date:  2001-01       Impact factor: 7.640

  6 in total

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