Uh. Stenman et al., SERUM CONCENTRATIONS OF PROSTATE-SPECIFIC ANTIGEN AND ITS COMPLEX WITH ALPHA(1)-ANTICHYMOTRYPSIN BEFORE DIAGNOSIS OF PROSTATE-CANCER, Lancet, 344(8937), 1994, pp. 1594-1598
Prostate cancer can be detected at an early, potentially curable stage
by screening based on digital rectal examination and serum prostate s
pecific antigen (PSA). The value of screening appears doubtful, based
on high 10-year survival rates in selected cases of early prostate can
cer, but this follow-up time may be insufficient. By linking the infor
mation on 21172 men who took part in a screening examination in Finlan
d, 1968-73, with data from the Finnish Cancer Registry, 44 cases of pr
ostate cancer diagnosed up to 1980 were identified. Serum samples from
cancer cases and from 74 controls matched for age and time of samplin
g were assayed for PSA and its complex with alpha(1)-antichymotrypsin
(PSA-ACT). With a cut-off for PSA of 2.5 mu g/L giving 92% specificity
, 95% of the cancers developing within the first 5 years, and 52% deve
loping in 6-10 years tested positive. As a potential screening test wi
th a 5-year interval for men under 65, the sensitivity would be 92% an
d specificity 97%. The ratio of PSA-ACT to total PSA was lower in cont
rols than in patients wih cancer. Using this ratio, we could eliminate
half of the false-positive results in the range 2.5-25 mu g/L without
loss of sensitivity. Cancer was typically diagnosed 5-10 years after
PSA exceeded 2.5 mu g/L, and the median survival after diagnosis was 3
.6 years. 10-year survivat after drawing the sample was 71% in cancer
cases with a PSA concentration less than 4 mu g/L and 48% in those wit
h higher concentrations. The corresponding figures at 15 years were 53
% and 27%, and at 20 years 43% and 18%, respectively. These results su
ggest it is advisable to confine screening for prostate cancer to men
with a life expectancy of clearly more than 10 years-ie, younger men,
who have the greatest chance to benefit from early detection.