Purpose: We performed a study to determine whether postoperative mild
chemotherapy to maintain the patient's quality of life (QOL) and immun
oactivity could also prolong survival. Subjects and Methods: From Dece
mber 1985 to July 1988, 323 patients with completely resected primary
non-small-cell lung cancer (stage I to III) were enrolled. The subject
s were randomized into three treatment groups, as follows: cisplatin (
CDDP) 50 mg/m(2) body surface, vindesine (VDS) 2 to 3 mg/kg body weigh
t for three courses, and 1-year oral administration of tegafur (FT) pl
us uracil (UFT) 400 mg/kg body weight (CVUft group, 115 patients); 1-y
ear oral administration of UFT 400 mg/kg body weight (Uft group, 108 p
atients); or surgical treatment only (control group, 100 patients). Re
sults: The overall 5-year survival rates were 60.6% for the CVUft grou
p and 64.1% for the Uft group versus 49.0% for the control group. The
results of statistical testing were P = .053 (log-rank test) and P = .
044 (generalized Wilcoxon test) among the three groups, P = .083 (log-
rank) and P = .074 (Wilcoxon) between the CVUft and the control groups
, and P = .022 (log-rank) and P = .019 (Wilcoxon) between the Uft and
the control groups, which indicates higher survival rates in the CVUft
and the Uft groups compared with the control group. A multivariate st
atistical analysis on prognostic factors using Cox's proportional haza
rds model was performed with the following results: P = .037, hazards
ratio = 0.64 with a 95% confidence interval (CI) of 0.42 to 0.97 (cont
rol v CVUft group); and P = .009, hazards ratio = 0.55 with a 95% CI o
f 0.36 to 0.86 (control v Uft group). Conclusion: Significantly favora
ble results were obtained in the CVUft and Uft groups compared with su
rgery alone. These data showed significant prognostic advantages in th
e postoperative adjuvant chemotherapy groups. (C) 1996 by American Soc
iety of Clinical Oncology.