Test CINtec Plus Cytology
CINtec Plus is a screening immunocytochemical test complementary to LBC liquid cytology and is used to detect cancerous lesions caused by highly oncogenic human papillomavirus in the early stages of cancer development.
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What is the CINtec® Plus test?
The test is used to detect cancerous lesions caused by the high-oncogenic human papillomavirus in the early stages of cancer development. As a result of human papilloma virus (HPV) infection, the cellric cycle is disrupted. The test is performed on a liquid cytological medium. In the laboratory, the smear slide is subjected to a special procedure, whichra consists in appropriate staining of the cellsrek. Thanks to this, two biomarkers, p16 and Ki-67, are detected, which makes it possible to locate cellsrs that do not divide in a normal mannerb.
Who should take the CINtec® PLUS test?
The CINtec® PLUS test is intended for patients whor who:
- gynecologic cytology showed ASCUS, LSIL lesions
- with a normal cytology result, a positive test result for HPV was obtained
- no definite diagnosis can be made by cytology
The test should be ordered for clinical indications based on a physician's referral. In order to maintain the fullest interpretation of the CINtec® PLUS result, a sequence of tests is recommended
Benefits of performing the CINtec® PLUS test
- enables evaluation of the cellsrek at a very early stage of cancerous lesions
- less invasive and painless examination
- increased diagnostic capabilities
- minimization of abnormal or undiagnostic results
- saving time and cost– no need to repeat cytology
- reducing the likelihood of needing a colposcopic examination
Interpretation oftest results should be conducted by the physician based on the patient's clinical condition, therapies used, and diagnostic test results.