OVARIAN CANCER SCREENING USING ULTRASOUND AND CA125 FINDS BOTH EARLY AND LATE STAGE CANCERS, BUT ALSO MANY FALSE POSITIVES

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Cancer Institute (NCI) 
http://www.cancer.gov/

EMBARGOED FOR RELEASE: Monday, November 7, 2005; 12:01 a.m. ET

CONTACT: NCI Media Relations Branch, 301-496-6641,
ncipressofficers@xxxxxxxxxxxx  
 
OVARIAN CANCER SCREENING USING ULTRASOUND AND CA125 FINDS BOTH EARLY AND
LATE STAGE CANCERS, BUT ALSO MANY FALSE POSITIVES 

A new study from the National Cancer Institute (NCI), part of the
National Institutes of Health, shows that currently available screening
methods such as transvaginal ultrasound (TVU) and testing for a protein
biomarker called CA-125, alone or in combination, can detect ovarian
cancer but can also produce many false-positive test results, causing
needless surgery. This report, which summarizes preliminary results from
the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening
Trial, appears in the November 15, 2005 "American Journal of Obstetrics
and Gynecology"*. 

These findings, the first published ovarian cancer screening results
from NCI's ongoing multicenter PLCO Cancer Screening Trial, are based on
an analysis of the trial participants' initial screening tests. CA-125
and TVU have been considered as potential screening techniques, although
studies to date have not shown that they can be effective and thus they
are not currently recommended. The long-term objective of the PLCO Trial
is to determine whether screening with TVU and/or CA-125 decreases
ovarian cancer mortality in women age 55 to 74. 

Of the 28,816 healthy women who underwent the initial (baseline)
screening, 1338 (4.7 percent) had an abnormal TVU and 402 (1.4 percent)
had an abnormal CA-125 blood test. Thirty-four women (0.1 percent) had
abnormal results in both screening tests. Among the women with abnormal
test results, 29 tumors were detected, 20 of which were invasive
cancers. 

Women who had an abnormal test result in one or both screening tests
underwent a variety of diagnostic procedures to determine whether cancer
was present, including 570 women who underwent a surgical procedure as
follow-up. Thus, 541 women underwent surgery but did not have cancer. 

"Ovarian cancer is a disease that is often fatal, and both patients and
physicians are anxious to find ways to detect it at an earlier, more
curable stage," said first author on the study, Saundra Buys, M.D.,
University of Utah, Salt Lake City. "However, the results from the
initial year of screening show that TVU and CA-125 cannot currently be
recommended for widespread use in the general population. Future results
from the additional PLCO screenings and subsequent follow-up will be
needed before a final assessment of this screening strategy can be
made." 

Enrollment in the PLCO study began in 1993 and ended in 2001. When they
initially enrolled in the study, women in the intervention arm underwent
baseline ovarian cancer screening with CA-125 and TVU and received
additional annual screenings and follow-up. Women in the control arm of
the study were not screened but were observed over time. 

The results published in this report reflect analysis of the initial
baseline screenings for women enrolled between 1993 and 2001. The
results of subsequent years screening with TVU and CA-125 are not yet
available, and it is these additional results that will ultimately
determine whether this screening strategy is effective in reducing
mortality from ovarian cancer. These results will not be available for
several years. 

At the time of the baseline examination, both TVU and CA-125 had low
predictive values -- a measure of how likely a person with a positive
test result is to have the disease of interest -- when used to screen
healthy women for ovarian cancer. Many investigators feel that an
acceptable predictive value for an ovarian cancer screening test is
around 10 percent. The predictive values of these screening tests were
3.7 percent for an abnormal CA-125 test, 1 percent for an abnormal TVU,
and 23.5 percent if both tests were abnormal. Although having an
abnormality in both tests had a fairly high predictive value, only 9 of
the 29 tumors (31 percent) were associated with abnormalities in both
tests. 

Patricia Hartge, Sc.D., a NCI investigator on the PLCO project, added,
"As women are followed for a longer period of time, it will be possible
to examine how screening tests behave in special groups of women; for
example, those with breast or ovarian cancer in their family."
Investigators will also be able to study whether other biological
markers which are proposed but unconfirmed are useful for early
detection of ovarian cancer. 

The PLCO is currently scheduled to collect data until 2008. 

To view a fact sheet on the PLCO Cancer Screening Trial, please visit
http://www.cancer.gov/cancertopics/factsheet/Detection/PLCOOvarianFactSh
eet. 

For more information about cancer, visit the NCI Web site at
http://www.cancer.gov or call NCI's Cancer Information Service at
1-800-4 CANCER (1-800-422-6237). 

The National Institutes of Health (NIH) -- "The Nation's Medical
Research Agency" -- includes 27 Institutes and Centers and is a
component of the U. S. Department of Health and Human Services. It is
the primary Federal agency for conducting and supporting basic,
clinical, and translational medical research, and it investigates the
causes, treatments, and cures for both common and rare diseases. For
more information about NIH and its programs, visit http://www.nih.gov.
  
-----------------------------------------------
* Buys SS, Partridge E, et al. "Ovarian Cancer Screening in the
Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial:
Findings from the Initial Screen of a Randomized Trial." "American
Journal of Obstetrics and Gynecology". 
-----------------------------------------------

##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/nov2005/nci-07a.htm.

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