Italy Is First Country to Launch Government-Sponsored Cervical Cancer Screening Program Using HPV Test As Primary Diagnostic
June 13 2007 - 8:00AM
PR Newswire (US)
Pilot program now screening women in Tivoli area GAITHERSBURG, Md.,
June 13 /PRNewswire-FirstCall/ -- Italy has become the first
country to launch a government-sponsored cervical cancer screening
program using the HPV test as the frontline diagnostic tool,
followed by cytology (Pap) for women who are found to carry the
human papillomavirus (HPV), Digene Corp. (NASDAQ:DIGE) announced
today. The program focuses on women living in Tivoli -- an area
just outside of Rome -- and is organized by the Health Care Unit
ASL Roma G, the largest local health unit in Italy. The Digene(R)
HPV Test, which uses the company's proprietary Hybrid Capture(R) II
(hc2) technology, is the only test for detecting the presence of
high-risk types of HPV, the cause of cervical cancer, that is
clinically validated and both FDA-approved and CE-marked. In the
United States, it is approved for routine use along with a Pap in
women age 30 and older. However, since clinical evidence has shown
that HPV infection is necessary for the development of cervical
cancer and that HPV testing can identify women at risk for
developing the disease, Roma G has decided to test women age 25-64
for high-risk types of the virus before administering a Pap. A
number of medical experts, including the authors of a recent
consensus paper on HPV published in the journal Vaccine, have
predicted that this is the paradigm of the future for cervical
cancer screening. In the pilot phase of the program, 26,000 women
in the targeted age range who live in the jurisdiction of the Roma
G unit are being recruited for HPV testing via a letter and
educational information. Once the pilot is complete and outcomes
are assessed, primary HPV screening will be considered for
expansion to all eligible women in the area. "The (Italian) Public
Health Agency has identified our ASL Roma G unit as the pilot
center for the first use of the HPV test as a first-level screening
tool," said Dr. Maria Concetta Tufi, who is responsible for the
screening program of ASL Roma G. "It is a unique approach not only
for Italy but for the whole world. It's an innovation destined to
radically change the approach to cervical cancer prevention, with
an ambitious objective to eliminate a disease that kills
approximately 300,000 women around the world ever year, including
2,000 in Italy." While the Pap relies on a laboratory technician to
manually look for cell changes that may signal cervical disease,
the Digene HPV Test uses advanced molecular technology to identify
the presence of the genetic code (DNA) of 13 high-risk types of
HPV. Research shows that when used alone, the sensitivity of
cytology is highly variable, ranging from 50-85 percent. In
contrast, the sensitivity of the Digene HPV Test has been proven in
large-scale clinical trials to be 95-100 percent. About Digene A
leader in molecular diagnostics, Digene develops, manufactures and
markets proprietary DNA and RNA tests, with a focus on women's
health. The company's flagship product, the Digene(R) HPV Test, is
the only FDA-approved and CE-marked test for the human
papillomavirus, the cause of essentially all cervical cancers.
Digene's product portfolio also includes tests for the detection of
other sexually transmitted infections, including chlamydia and
gonorrhea. Digene tests are marketed in more than 40 countries
worldwide. Headquartered in Gaithersburg, MD, Digene is traded on
Nasdaq under the symbol DIGE. For more information, visit
http://www.digene.com/ and http://www.thehpvtest.com/. This press
release contains forward-looking statements within the meaning of
the Private Securities Litigation Reform Act of 1995. These
forward-looking statements are not guarantees of the future as
there are a number of meaningful factors that could cause the
company's actual results to vary materially from those indicated by
such forward-looking statements. Meaningful factors, which could
cause actual results to differ from expectations include, but are
not limited to, the degree of acceptance of HPV testing by
physicians, uncertainty of the company's future profitability, its
ability to scale up manufacturing operations to meet any increased
demand, the uncertainty regarding patents and proprietary rights,
the success of the company's marketing efforts, competition, risks
inherent in international transactions, and the inability to obtain
requisite additional financing, as well as other factors discussed
in the company's Securities and Exchange Commission filings. For
other factors, reference is made to the discussion in the company's
annual and quarterly reports filed with the Securities and Exchange
Commission. DATASOURCE: Digene Corporation CONTACT: Albert Fleury,
Investor Relations, +1-301-944-7000; Media - Pam Rasmussen,
+1-301-944-7196, both of Digene Corporation Web site:
http://www.digene.com/ http://www.thehpvtest.com/
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