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
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.