Cure rate estimation is an important issue in clinical trials for dise
ases such as lymphoma and breast cancer and mixture models are the mai
n statistical methods. In the last decade, mixture models under differ
ent distributions, such as exponential, Weibull, log-normal and Gomper
tz, have been discussed and used. However, these models involve strong
er distributional assumptions than is desirable and inferences may not
be robust to departures from these assumptions. In this paper, a mixt
ure model is proposed using the generalized F distribution family. Alt
hough this family is seldom used because of computational difficulties
, it has the advantage of being very flexible and including many commo
nly used distributions as special cases. The generalised F mixture mod
el can relax the usual stronger distributional assumptions and allow t
he analyst to uncover structure in the data that might otherwise have
been missed. This is illustrated by fitting the model to data from lar
ge-scale clinical trials with long follow-up of lymphoma patients. Com
putational problems with the model and model selection methods are dis
cussed. Comparison of maximum likelihood estimates with those obtained
from mixture models under other distributions are included. (C) 1998
John Whey & Sons, Ltd.