The overall 5-year survival of surgically resected non-small cell lung
cancer (NSCLC) remains less than 50% and is unlikely to improve until
there are effective systemic adjuvant therapies. Two studies of the L
ung Cancer Study Group (LCSG) have shown a modest impact of adjuvant C
AP chemotherapy on disease-free and overall survival. In addition, a F
innish study, which randomized patients with T1-T3, NO disease to CAP
chemotherapy or follow-up, has also demonstrated an improvement in rec
urrence-free survival, as well as overall survival, at 5 and 10 years.
On the other hand, an LCSG trial of adjuvant CAP in Stage I NSCLC (T2
NO, T1 N1) showed no benefit, although compliance with treatment was
poor. Similarly, adjuvant trials using vindesine and cisplatin have no
t demonstrated benefit in studies done in Montreal and New York. Clear
ly, more effective systemic therapy is needed and must be evaluated in
randomized trials in which patients have been carefully staged intra-
operatively. Biological markers, such as vascular invasiveness, oncoge
ne mutations and other factors may allow identification of specific su
bsets of patients at high risk of recurrence who can be targeted for a
ggressive adjuvant approaches in the future.