CONTROLLED CLINICAL-TRIALS WITH FENRETINIDE IN BREAST-CANCER, BASAL-CELL CARCINOMA AND ORAL LEUKOPLAKIA

Citation
G. Depalo et al., CONTROLLED CLINICAL-TRIALS WITH FENRETINIDE IN BREAST-CANCER, BASAL-CELL CARCINOMA AND ORAL LEUKOPLAKIA, Journal of cellular biochemistry, 1995, pp. 11-17
Citations number
16
Categorie Soggetti
Biology
ISSN journal
07302312
Year of publication
1995
Supplement
22
Pages
11 - 17
Database
ISI
SICI code
0730-2312(1995):<11:CCWFIB>2.0.ZU;2-F
Abstract
We are conducting three randomized studies (breast cancer, basal cell carcinoma, oral leukoplakia) and report our methodological approach an d accrual here. The aim of the breast cancer study is prevention of a contralateral primary lesion in women already treated for breast cance r; the aim of the basal cell carcinoma study is prevention of recurren ces or new occurrence after surgical resection; and the aim of the ora l leukoplakia study is prevention of recurrences and new occurrence af ter CO, laser resection. The studies were planned according to a rando mized design with an intervention arm vs a no-treatment arm. Patients in the intervention group receive 4-HPR at a dose of 200 mg po. The du ration of treatment is five years in the breast cancer study, and one year in the basal cell carcinoma and oral leukoplakia studies. The bre ast cancer study started in March 1987, closing accrual on July 31, 19 93. A total of 2,972 patients entered the study; 2,849 were evaluable (1,422 in the 4-HPR group and 1,427 in the control group). Of 2,849 ev aluable patients, 867 completed the first five years, 1,142 are still ongoing, and 840 patients have interrupted the study for various reaso ns. Follow-up is ongoing. The basal cell carcinoma study started in Ja nuary 1990. As of January 1994, a total of 786 patients had entered th e study; 760 were evaluable (363 in the 4-HPR group and 367 in the con trol group). Of 760 patients in the study, 568 completed the first yea r, 62 are ongoing and 130 discontinued for various reasons. The study is ongoing. The oral leukoplakia study started in September 1988, dosi ng accrual on February 1, 1994. A total of 174 patients entered the st udy; 170 were evaluable (84 in the 4-HPR group and 86 in the control g roup). The preliminary data of this study have been published. Updated results as of June 1994 were 11 recurrences and three new occurrences in the 4-HPR group; the control group also had 11 recurrences, as wel l as 12 new occurrences. Follow-up is ongoing. (C) 1995 Wiley-Liss, In c.