A study by Karolinska Institutet and Queen Mary University of London, published in PLOS Medicine, has introduced a method to classify HPV-positive women into risk groups, improving cervical cancer screening. Key findings and details include:
Study Overview
- The study involved 855 HPV-positive women in England who participated in a self-testing trial due to overdue cervical screenings.
- Among them, 71 women (8.3%) were diagnosed with severe cervical precancer or cancer.
Risk Stratification
The new method categorized women into high, medium, and low-risk groups using – HPV variant type and Viral load (cycle threshold, Ct value).
High-risk group:
- Women with HPV type 16 and Ct values <30.
- 40% had severe precancer or cancer, requiring immediate colposcopy.
Low-risk group:
- Over 50% of HPV-positive women.
- Only 4% risk of severe disease within 12 months.
- Suggested follow-up: annual retesting.
Medium-risk group:
- Recommended clinical testing.
Advantages of the Method
Risk assessment can be performed immediately after HPV self-testing, eliminating the need for further lab analyses. This can be particularly beneficial for low-and middle-income countries with limited resources.
Importance for India
- India accounts for nearly one-fifth of the global cervical cancer burden, with over 1,20,000 cases annually.
- HPV self-testing is a cost-effective, scalable solution, especially in rural areas where access to routine screenings is limited.
- This method can bridge gaps in healthcare by identifying high-risk women early and reducing the workload on overburdened healthcare systems.
- The ability to conduct risk assessment immediately after self-testing makes it ideal for mass implementation in India’s resource-constrained settings.
Conclusion
Self-testing for HPV is a powerful tool that ensures broader participation in cervical cancer screening, especially among women who might otherwise miss routine tests. By enabling targeted interventions for high-risk cases, this approach not only improves early detection but also enhances the overall efficiency of cervical cancer screening programs, ultimately saving lives.
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