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Feasibility study of docetaxel and nedaplatin for recurrent squamous cell carcinoma of the uterine c
BACKGROUND: To determine a new taxane plus platinum treatment regimen for squamous cell carcinoma of the uterine cervix (CSCC), a phase I feasibility study of docetaxel (DTX) plus nedaplatin (CDGP) combination therapy was conducted. PATIENTS AND METHODS: Twenty consecutive patients were enrolled into the study. The starting dose of DTX/CDGP was 60 mg/m2 / 80 mg/m2, every 4 weeks for at least three courses and the dose was escalated to 70 mg/m2 / 100 mg/m2. DTX 60 mg/m2 / CDGP 100 mg/m2 was also evaluated as an extra dose level. RESULTS: Dose-limiting toxicity was granulocytopenia and the maximum tolerated dose was determined as 70 mg/m2 / 100 mg/m2. All 20 patients had measurable disease and a partial response was achieved in 8 (40.0%) patients. CONCLUSION: DTX/CDGP therapy appears to be a tolerable regimen for cervical squamous cell carcinoma, even in patients previously treated by cisplatin concurrent chemoradiotherapy. The recommended doses of DTX and CDGP were determined to be 60 mg/m2 and 100 mg/m2, respectively.
377-2 Ohno-Higashi Osakasayama Osaka 589-8511 Japan
Departments Name: Department of Obstetrics and Gynecology
Institution name: Kinki University School of Medicine
Authors: Watanabe Y, Nakai H, Etoh T, Kanemura K, Tsuji I, Ishizu A, Hoshiai H.
Journal Name: Anticancer Res.
Data: 2008, Jul-Aug
Volume: 28(4C):2385-8
Country: Japan
Other Categories:
Cervical Cancer
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