Academic Journal

Randomized phase II trial of iproplatin and carboplatin in advanced breast cancer

التفاصيل البيبلوغرافية
العنوان: Randomized phase II trial of iproplatin and carboplatin in advanced breast cancer
المؤلفون: Vermorken, J. B., Gundersen, S., Clavel, M., Smyth, J. F., Dodion, P., Renard, J., Kaye, S. B., For the EORTC Early Clinical Trials Group and the EORTC Data Center
بيانات النشر: Oxford University Press
سنة النشر: 1993
المجموعة: HighWire Press (Stanford University)
مصطلحات موضوعية: Original articles
الوصف: Background: The observed activity of cisplatin in breast cancer and its unattractive toxicity profile in palliative treatment warranted further study of platinum analogues in this disease. Patients and methods: Sixty-two patients with recurrent or metastatic breast cancer, 61 of whom had been previously treated with chemotherapy, were randomly assigned to therapy with either iproplatin (n = 32) or carboplatin (n = 30). Both platinum analogues were administered intravenously, iproplatin at a dose of 240 mg/m2 every 4 weeks and carboplatin at a dose of 450 mg/m2 every 5 weeks. Results: Only two patients responded to iproplatin (7%) for durations of 21 and 61 weeks, and one patient responded to carboplatin (3%) for a duration of 64 weeks. All responses were complete. At the given dose schedules carboplatin was more myelosuppressive than iproplatin. Non-hematologic toxicities included nausea and vomiting (93% vs. 90%), diarrhea (20% vs. 10%) and hemorrhage (16% vs. 10%) for iproplatin and carboplatin, respectively. Two patients developed alopecia with carboplatin. No renal toxicity was observed. Conclusions: Both iproplatin and carboplatin have limited activity in previously treated women with advanced breast cancer when given in conventional dosages.
نوع الوثيقة: text
وصف الملف: text/html
اللغة: English
Relation: http://annonc.oxfordjournals.org/cgi/content/short/4/4/303
الاتاحة: http://annonc.oxfordjournals.org/cgi/content/short/4/4/303
Rights: Copyright (C) 1993, European Society for Medical Oncology
رقم الانضمام: edsbas.D38C24D0
قاعدة البيانات: BASE