NEUROTOXICITY IN A PHASE-I TRIAL OF CONTINUOUS-INFUSION CISPLATIN WITH HYPERFRACTIONATED RADIOTHERAPY FOR LOCALLY ADVANCED HEAD AND NECK-CANCER

Citation
Gh. Clamon et al., NEUROTOXICITY IN A PHASE-I TRIAL OF CONTINUOUS-INFUSION CISPLATIN WITH HYPERFRACTIONATED RADIOTHERAPY FOR LOCALLY ADVANCED HEAD AND NECK-CANCER, Head & neck, 18(3), 1996, pp. 236-241
Citations number
20
Categorie Soggetti
Surgery,Otorhinolaryngology
Journal title
ISSN journal
10433074
Volume
18
Issue
3
Year of publication
1996
Pages
236 - 241
Database
ISI
SICI code
1043-3074(1996)18:3<236:NIAPTO>2.0.ZU;2-1
Abstract
Background. Both twice daily fractionated radiotherapy and concurrent cisplatin with once-daily radiotherapy have been shown to improve loca l disease control in patients with head and neck cancer. The objective of this phase I trial was to determine the maximum tolerated dose of cisplatin which could be given as a continuous infusion concurrent wit h twice-daily radiotherapy to patients with locally advanced head and neck cancer. Methods. Patients were treated with radiotherapy at doses of 110 cGy twice daily for 5 days per week to a total dose of 7040-75 90 cGy. Concurrent with radiotherapy, patients received continuous-inf usion cisplatin for 5 days per week. Groups of 3-6 patients were treat ed with doses of 1-3 mg/m(2)/day. Results. Central nervous system toxi city became dose-limiting. At 1 mg/m(2), 2 mg/m(2), and 3 mg/m(2) conf usion was observed and one patient had a seizure. At 3 mg/m(2), anothe r patient suffered severe sensory and motor neuropathy. Despite bulky tumors, 12 of the 14 patients had an objective response and 3 achieved a complete response. Conclusions. The combination of twice-daily frac tionated radiotherapy and concurrent cisplatin by continuous infusion is severely toxic and achieves results similar to less toxic programs. It is not recommended for further investigation or therapy.