TUCSON, Ariz., June 16, 2015 /PRNewswire/ -- Ventana
Medical Systems, Inc. (Ventana), a member of the Roche Group, today
announced the publication of further results from the Primary
ASC-US LSIL Marker Study (PALMS) in this month's issue of Cancer
Cytopathology1. The PALMS study, which enrolled more
than 27,000 women from five European countries, was designed to
evaluate the diagnostic performance of the CINtec® PLUS
Cytology2 test in detecting pre-cancerous cervical
disease compared to HPV testing and more traditional screening
methods like Pap cytology.
In this latest publication based on the PALMS study results, the
CINtec PLUS Cytology test was compared to pooled, high-risk
HPV DNA testing as a triage or follow-up screening method for
mildly abnormal Pap cytology results. The study confirmed that the
CINtec PLUS Cytology test had significantly higher
specificity and was more effective overall than the HC2 HPV test in
identifying women with precancerous lesions. These results suggest
that if implemented as a triage test in a cytology-based screening
program, the CINtec PLUS Cytology test may lead to a
reduction in the overtreatment of women screened for cervical
disease.
"These latest results of PALMS confirm data from previous
studies which have shown that incorporating the CINtec PLUS
Cytology test in cervical cancer screening programs can provide
real benefit to both clinicians and their patients," says Dr.
Christine Bergeron, Laboratoire
Cerba, Cergy Pontoise, France,
PALMS study investigator and publication author. "As a triage
test for abnormal cervical cancer screening results, the CINtec
PLUS Cytology test could be very useful to differentiate
women who will benefit most from immediate referral to colposcopy
and diagnostic follow-up, from those women who can be followed up
with less invasive methods."
More than 500,000 new cases of cervical cancer are diagnosed
each year worldwide3 and the average five-year survival
rate of patients is only around 50%.3 HPV infections are
common and cause virtually all cervical cancer3;
however, only those women with persistent HPV infections and who
have developed high-grade precancerous cervical disease should be
treated. The CINtec PLUS Cytology test was developed to help
identify the subgroup of women with underlying transforming HPV
infections that may lead to cancer and distinguish them from those
with mostly transient infections.
"The results observed in PALMS are consistent with those
demonstrated in many other published studies" said Tim Himes, Lifecycle Leader,
CINtec and HPV-mediated Disease. "As countries begin to
move towards primary screening with HPV, the need for an improved
triage test will increase dramatically. We are therefore
pleased to see that the CINtec PLUS Cytology test
consistently demonstrates strong performance when used in the
triage setting. By overcoming the known issues with Pap
cytology, the test is well positioned to provide immediate benefit
to women, doctors and screening programs globally."
1Bergeron, C., Ikenberg, H., Sideri, M., Denton, K.,
Bogers, J., Schmidt, D., Alameda,
F., Keller, T., Rehm, S., Ridder, R. and for the PALMS Study Group.
Prospective evaluation of p16/Ki-67 dual-stained cytology for
managing women with abnormal Papanicolaou cytology: PALMS study
results. Cancer Cytopathol. 2015; 123(6):373-381.
2The CINtec® PLUS Cytology test is not
available in all geographies.
3 World Health Organization Fact Sheet 380,
March 2015:
http://www.who.int/mediacentre/factsheets/fs380/en/
About Ventana Medical Systems, Inc.
Ventana Medical
Systems, Inc. ("VMSI"), a member of the Roche Group (SIX: RO, ROG;
OTCQX: RHHBY), innovates and manufactures instruments and reagents
that automate tissue processing and slide staining for cancer
diagnostics. VENTANA products are used in clinical histology and
drug development research laboratories worldwide. The company's
intuitive, integrated staining, workflow management platforms, and
digital pathology solutions optimize laboratory efficiencies to
help reduce errors, support diagnosis and enable informed treatment
decisions by anatomic pathology professionals. Together with Roche,
VMSI is driving Personalized Healthcare through accelerated drug
discovery and the development of companion diagnostics to identify
the patients most likely to respond favorably to specific
therapies.
Visit www.ventana.com to learn more.
About Roche
Headquartered in Basel, Switzerland, Roche is a leader in
research-focused healthcare with combined strengths in
pharmaceuticals and diagnostics. Roche is the world's largest
biotech company, with truly differentiated medicines in oncology,
immunology, infectious diseases, ophthalmology and neuroscience.
Roche is also the world leader in in vitro diagnostics and
tissue-based cancer diagnostics, and a frontrunner in diabetes
management. Roche's personalised healthcare strategy aims at
providing medicines and diagnostics that enable tangible
improvements in the health, quality of life and survival of
patients. Founded in 1896, Roche has been making important
contributions to global health for more than a century.
Twenty-eight medicines developed by Roche are included in the World
Health Organization Model Lists of Essential Medicines, among them
life-saving antibiotics, antimalarials and chemotherapy.
In 2014, the Roche Group employed 88,500 people worldwide,
invested 8.9 billion Swiss francs in
R&D and posted sales of 47.5 billion
Swiss francs. Genentech, in the
United States, is a wholly owned member of the Roche Group.
Roche is the majority shareholder in Chugai Pharmaceutical,
Japan. For more information,
please visit www.roche.com.
All trademarks used or mentioned in this release are protected
by law.
VMSI Media Relations
Jacquie Bucher
Vice President, Marketing and Corporate Communications
Ventana Medical Systems, Inc.
A Member of the Roche Group
Phone: 520-247-4085
e-mail: jacquie.bucher@ventana.roche.com
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SOURCE Ventana Medical Systems, Inc.