To view associated reagents, ancillaries and bulks, please visit the Roche Tissue Diagnostics reagent catalog.
Be certain – Triage with CINtec® PLUS Cytology
Unique dual-biomarker technology makes you certain about the presence of transforming HPV infection.
CINtec® PLUS Cytology is the only test that uses dual-biomarker technology to simultaneously detect p16 and Ki-67 to provide a strong indicator of the presence of transforming HPV infections.
Co-expression of p16 and Ki-67 in the same cell is strongly associated with established high-grade disease.
T.C. Wright Jr. et al., Triaging HPV-Positive Women with p16/Ki-67 Dual-stained Cytology: Results from a Sub-study Nested into the ATHENA Trial. Gynecologic Oncology 144 (2017) 51–56.
A retrospective study comparing the results of CINtec® PLUS Cytology vs. Pap cytology triage of HPV (+) test results from a subset of samples collected in the ATHENA Trial. Results are correlated to histology follow-up reported in the ATHENA data.
Ikenberg, H. et al., Screening for Cervical Cancer Precursors With p16/Ki-67 Dual-Stained Cytology: Results of the PALMS Study. J Natl Cancer Inst. 2013 Oct 16; 105(20): 1550–1557.
The PALMS study (Primary ASC-US and LSIL Marker Study) validated the CINtec® PLUS Cytology test in 27,349 women from five European countries enrolled in the prospective study to show performance of Pap cytology, p16/Ki-67 immunostaining and HPV testing. Presence of ≥CIN2 disease on adjudicated histology was used as the reference standard.
2. An objective biomarker test to help triage Pap negative/HPV (+) co-testing results
Improve management of women with Pap cytology negative/HPV (+) results: In co-testing, CINtec® PLUS Cytology provides immediate and actionable results to help reduce the number of women lost to follow-up testing.
3. CINtec® PLUS Cytology outperforms Pap cytology as the triage test for HPV (+) screening results
Improved cervical cancer screening strategy: Primary screening by the cobas® HPV DNA test with triage using the CINtec® PLUS Cytology test demonstrates high sensitivity and specificity to detect transforming HPV infections and helps avoid unnecessary colposcopy for women who do not need it.
The following publications provide further evidence of the clinical utility of p16/Ki-67 dual staining in cervical cancer screening:
*CINtec® PLUS Cytology is a CE/IVD product, approved for clinical use. CINtec® PLUS Cytology is not available for this use in the United States. Check with your local Roche representative for the availability of products in your region and the applicable intended use