Background. Patients with advanced, inoperable head and neck cancers have cure rates of approximately 10-15%. In these patients, concomitant chemoradiotherapy seems to improve local control and survival. 5-Fluorouracil(5-FU) administered by continuous infusion and cisplatin plus concomitant conventi
Concomitant radiochemotherapy in primary inoperable advanced head and neck cancer with 5-fluorouracil and mitomycin-C
β Scribed by Hans Christiansen; Robert M. Hermann; Andrea Hille; Elisabeth Weiss; Mirko Nitsche; Alexios Martin; Clemens F. Hess; Olivier Pradier
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 534 KB
- Volume
- 26
- Category
- Article
- ISSN
- 1043-3074
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β¦ Synopsis
Abstract
Background.
The purpose of this study was to evaluate the efficacy and toxicity of radiotherapy and concomitant 5βfluorouracil (5βFU) and mitomycinβC infusion in inoperable head and neck cancer.
Methods.
Seventyβsix patients (86% men, 14% women), mean age 57 years, with primary inoperable head and neck cancer were treated with 70 Gy plus simultaneous intravenous chemotherapy with 5βFU (600 mg/m^2^/d, days 1 to 5) and mitomycinβC (10 mg/m^2^, day 5 plus 36).
Results.
After a mean followβup of 13 months, 31 patients were alive. Complete response (CR) was seen in 63%. The 1β and 2βyear overall survival rates were 67.7% and 39.5%, and locoregional control rates were 51.7% and 35.6%. Pretreatment hemoglobin <13.9 g/dL was associated with lower locoregional control rates (p = .03). Therapy was well tolerated (grade 3 mucositis in 21%, grade 4 in 1%, grade 3 leukopenia in 11%).
Conclusions.
Our radiochemotherapy regimen offers a curative option for this group of patients with a poor prognosis. Hemoglobin levels before therapy have an influence on prognosis. Β© 2004 Wiley Periodicals, Inc. Head Neck 26: 845β853, 2004
π SIMILAR VOLUMES
Thirty patients with advanced measurable colorectal cancer received monthly courses of a combination of dacarbazine, mitomycin C, 5-fluorouracil, and vincristine (FIVMit-Or). Four of the patients had received prior chemotherapy. Two patients were not evaluable for response. Objective response was ob