We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




Cervical Cancer Screening Could Become Less Frequent

By LabMedica International staff writers
Posted on 04 Nov 2016
Less-intensive screening is needed among women who have been vaccinated against human papillomavirus (HPV), which causes almost all cases of cervical cancer, because the risk of these women developing cervical cancer is quite low.

Since 2012, major guideline-making organizations have recommended that all women in the USA be screened for cervical cancer every three years beginning at age 21 with a Papanicolaou test (Pap test), which checks for abnormal cells in the cervix, with the option of switching to a combination of Pap test and HPV testing (known as "co-testing") every five years beginning at age 30.

Scientists at the Harvard T.H. More...
Chan School of Public Health (Boston, MA, USA) developed a disease simulation model to estimate the risks and benefits of various screening protocols. Their model projected the health and economic effects of three different types of HPV vaccines that are currently approved for use, two of which have been available since 2006. The goal was to pinpoint screening strategies that would provide the biggest health benefit in the most cost-effective way. Cost-effectiveness analysis was conducted from the societal perspective to identify screening strategies that would be considered good value for money according to thresholds of USD 50,000 to USD 200,000 per quality-adjusted life-year (QALY) gained.

The team found that among women fully vaccinated with the bivalent or quadrivalent vaccine, optimal screening strategies involved either cytology or HPV testing alone every five years starting at age 25 or 30 years, with cost-effectiveness ratios ranging from USD 34,680 to USD 138,560 per QALY gained. Screening earlier or more frequently was either not cost-effective or associated with exceedingly high cost-effectiveness ratios. In women vaccinated with the nonavalent vaccine, only primary HPV testing was efficient, involving decreased frequency (i.e., every 10 years) starting at either age 35; with lower nonavalent vaccine efficacy, 10-year HPV testing starting at earlier ages of 25 or 30 years was optimal. Importantly, current USA guidelines for screening were inefficient in HPV-vaccinated women.

Jane J. Kim, PhD, a professor and lead author of the study, said, “This analysis enabled us to examine what would happen if we shifted from the current way we screen for cervical cancer - essentially, recommending the same type of screening for all women - to screening that takes into account whether women have been vaccinated against HPV and therefore face a substantially lower risk of cervical cancer. We found that continuing intensive screening among HPV-vaccinated women yields excessive costs and harms with little to no health benefit. ” The study was published on October 17, 2016, in the Journal of the National Cancer Institute.

Related Links:
Harvard T.H. Chan School of Public Health


New
Gold Member
Clinical Chemistry Assay
Sorbitol Dehydrogenase (SDH)
POC Helicobacter Pylori Test Kit
Hepy Urease Test
New
Urine Analyzer
respons® UDS100
New
Creatinine/eGFR Meter
StatSensor® Creatinine/eGFR Meter
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Molecular Diagnostics

view channel
Image: The assay serves as an adjunctive tool in evaluating patients suspected of B-cell lymphoproliferative disorders (photo courtesy of Shutterstock)

First IVDR‑Certified IGH Clonality Assay Supports Diagnosis of B-Cell Malignancies

Accurate identification of clonal immunoglobulin heavy chain (IGH) gene rearrangements is central to evaluating suspected B-cell lymphoproliferative disorders, where a single B-cell clone yields a defining... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.