Background: The evolution of the management of advanced ovarian carcin
oma over the last fifteen years has resulted from a number of well-des
igned randomized trials involving large numbers of patients. Materials
and methods: A critical review of long-term follow-up of patients ent
ered onto eleven major randomized trials of advanced ovarian carcinoma
has been performed. Results: In the pre-platinum era no long-term sur
vival benefit was obtained with combination compared with single agent
chemotherapy. When adding cisplatin to front-line therapy at least a
short-term gain in terms of superior response rate and progression-fre
e intervals is obtained compared with non-cisplatin combination chemot
herapy. Survival data are more difficult to assess due to the use of c
is-platin-containing salvage therapy. Cisplatin-based combination ther
apy also offers enhanced patient benefit when compared with cisplatin
alone. A slight advantage favouring anthracycline-containing therapy i
s observed, whereas no advantage is obtained with alternating cisplati
n and non-cisplatin regimens or by adding BCG. Conclusions: Platinum-b
ased combination chemotherapy is clearly associated with improved resp
onse rates and progression-free survival and, at least in some studies
, better overall survival. At least six cycles of therapy should be gi
ven. Such approaches should yield long-term survival rates of 10% or b
etter for patients with large-volume disease and 20% or better for sma
ll-volume disease.