-
Clinical Trial Controlled Clinical Trial
[Atypical fractionation in advanced squamous-cell carcinomas of the head-neck area].
- W Dobrowsky, J Naudé, W Millesi, M Grasl, W Köhler, M Kautzky, R Pavelka, M Toth, and E Dobrowsky.
- Universitätsklinik für Strahlentherapie und Strahlenbiologie, Wien.
- Strahlenther Onkol. 1992 Dec 1; 168 (12): 686-91.
AbstractFrom May 1990 to May 1991, 23 patients with advanced, inoperable squamous cell cancers, clinically staged as III or IV, were treated by unconventional fractionation radiotherapy. Treatment consisted of a continuous hyperfractionated accelerated radiotherapy, delivering a total dose of 55.3 Gy within 17 consecutive days. In ten patients radiation therapy was combined with chemotherapy; 20 mg mitomycin C/m2, administered by intravenous bolus injection on day 5 of treatment. Apart from a confluent mucositis, treatment tolerance was good. Haematological toxicity from mitomycin C was minor and did not require any specific therapy. The mucosal reaction lasted six weeks (median duration) and was not thought to be increased by additional chemotherapy. In twelve of 23 patients a complete remission of the primary tumour was seen, in patients with lymph node metastases there was a complete response in 14 out of 20 patients. After a median follow-up of 18 months, ten of 23 patients have survived (8/23 without evidence of disease). Eleven patients have died due to local tumour progression and one patient died with distant metastases, being without evidence of local tumour. The advantage of this unconventional fractionation, which takes the described short potential tumour doubling time for head and neck cancers into account, is discussed.
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