
September 19, 2000
MEDIA CONTACT: Marjorie Centofanti
PHONE: (410) 955-8725
E-MAIL: mcentofanti@jhmi.edu
"...strong evidence indeed that what we're doing now is probably not the
best way"
The standard, widely-used approach to screen men for
prostate cancer --
annual PSA tests after age 50 -- may be less efficient
and cost-effective
than one that tests men earlier and less frequently,
according to a study
in today's Journal of the American Medical
Association.
The study used a computer model to simulate the outcomes of
prostate cancer
detection under a variety of scenarios. Researchers varied
the age at
which men would first start regular PSA testing, varied the
interval
between tests and varied the PSA cutoff level urologists use for
recommending a biopsy.
The favored scenario showed that screening men
twice before they're 50 --
once at age 40 and again at age 45 -- and then
following that with
every-other-year screening, beginning at age 50, "would
substantially
reduce the cost we spend on prostate screening. It would also
prevent more
deaths from prostate cancer, compared with existing screening
practices,"
says Hopkins urologist H. Ballentine Carter, M.D., a member of
the research
team.
Compared with the standard way of screening, he
says, "the model showed
you'd do 3,000 fewer PSA tests and 200 fewer
biopsies for every 1,000 men
screened over a lifetime."
"What we've
found doesn't mean the world should change screening practices
tomorrow. It
is, after all, a computer simulation," Carter adds. "But
because this
simulation is trustworthy, it's very strong evidence indeed
that what we're
doing now is probably not the best way."
Researchers from Johns Hopkins,
Merck Research labs and the University of
North Carolina collaborated on the
study.
Under current guidelines for prostate cancer screening, men get an
annual
PSA (prostate specific antigen) test after age 50, with a follow-up
biopsy
if the PSA level is higher than 4 nanograms per milliliter of blood.
"There's no science to show that you should start at age 50 and test
annually," says Carter. "That strategy was adopted because it seemed
reasonable, especially in light of women getting an annual mammogram for
breast cancer. But," he adds, "prostate cancer tends to grow and progress
more slowly than breast cancer, so yearly screening is probably not
necessary."
"In fact," Carter adds, "no good clinical research exists to
confirm that
PSA screening in general reduces deaths from prostate cancer.
Such very
expensive randomized studies, where large numbers of patients are
followed,
are now under way in Europe and the United States. But our study
assumes
PSA screening is useful and goes on to focus on the best way to do
it."
The model simulated a population of 1 million men, followed,
beginning at
age 40, for 40 years.
Under the "ground rules" the
researchers used as a basis for their model --
real data on the way prostate
cancer progresses over the years, on results
of treatment, on who gets the
disease, on what PSA tests and biopsies can
show -- the researchers first
produced a basic model of the natural history
of unchecked prostate cancer.
"That's what you'd get with no screening,"
says Carter.
Then they
modeled different PSA screening strategies. The researchers
compared each
strategy, with outcomes translated into the number of deaths
it would
prevent and into the number of PSA tests and biopsies that
strategy
required.
The researchers began their work because one of Carter's
earlier studies
showed younger men tend to have a higher cure rate from
prostate cancer,
probably because their tumors are smaller and more
confined. "Screening
earlier and detecting the disease at a younger age may
decrease the number
of deaths from prostate cancer in this country," says
Carter.
"We can't translate this yet into universal guidelines. The
purpose of
this study now is to raise awareness. What needs to take place
are
confirmatory studies with real patients. But based on this study, some
physicians and their patients may choose to begin PSA testing before age
50."
The research was funded by grants from the National Cancer
Institute.
Other researchers were Kevin S. Ross, now a medical student at
Hopkins and
formerly with the University of North Carolina, Chapel Hill;
Harry A.
Guess, with the University of North Carolina and the Merck Research
labs in
Blue Bell, Pa.; and Jay Pearson, Ph.D., with Hopkins and
Merck.
Related Web sites:
For more information on prostate research at
Hopkins:
http://prostate.urol.jhu.edu/
For
information on PSA testing and prostate cancer:
http://www.cancer.org/m2m/m2mpsa.html
or
http://www.afud.org/conditions/psaduring.html
TC-KA3ES