FC 17-11COMPARATIVE PERFORMANCE EVALUATION OF SCREENING TOOLS FOR POINT OF CARE CERVICAL CANCER SCREENING AND PRE CANCER TREATMENT AMONG WOMEN LIVING WITH HIV : CASE FOR INTEGRATING CERVICAL CANCER SCREENING WITH HIV TESTING AND COUNSELING CENTERS IN RESOURCE LIMITED SETTINGS .

13. Screening methods
S. Pimple 1, G. Mishra 1.
1Department of Preventive Oncology, Tata Memorial Centre (India)

Background / Objectives

Human Immunodeficiency Virus (HIV) related immunosuppression predisposes co-infection with Human Papillomavirus (HPV) and  increases  the risk of cervical intraepithelial neoplasia (CIN) and  cervical cancer. Centers for Disease Control (CDC) has included invasive cervical carcinoma among the AIDS-defining conditions. India shares 25% of global burden of cervical cancer  and  a third large burden of  HIV-infected women [1,2] who  currently continue to live longer due to improved access to antiretroviral therapy.  A cross-sectional study was performed to determine the prevalence of HPV infection, risk of cervical pre-cancer and  clinical performance  validation of Visual Inspection with Acetic Acid (VIA), Pap cytology and HPV tests   among women living with HIV/AIDS in Mumbai, India.


Methods

 309 HIV Positive women attending cervical cancer screening services in a tertiary care centre between 2009-12 were enrolled for cervical cancer screening  using Visual inspection with acetic acid (VIA), Pap cytology and HPV testing.  Total 291 HIV Positive women were included in the analysis. 18 were excluded from analysis for incomplete investigations. Screen positive women by either of the screening tests were subjected to  histopathology confirmation with colposcopy guided  cervical punch biopsy.


Results

Screen positivity rate for cervical cancer screening by VIA ,HPV DNA and Conventional Cytology  test was 36.1% (105) ,  32.3% (94) and 16.4% (48) respectively. Using a Histopathology CIN 2+ threshold, the sensitivity of VIA, HPV DNA and Conventional  cytology tests were  0.96 (95% CI: 0.78 - 1.00), 0.91 (95% CI: 0.71 - 0.99)  ,0.64 (95% CI: 0.41 - 0.83) and  specificities were   0.70 (95% CI: 0.64 - 0.76), 0.71 (95% CI: 0.65 - 0.76), 0.98 (95% CI: 0.95 - 0.99)  respectively. 


Conclusion

The prevalence of HPV infection and CIN are significantly higher in the HIV-positive women in India. VIA  performed equivalently to currently approved but  expensive HPV DNA tests and was highly  sensitive compared to conventional cytology. HPV DNA and cytology  are currently not feasible in low resource settings due to its logistics, financial and technical  requirements. It is feasible to integrate low cost VIA  as a point of care cervix cancer screening  modality that  facilitate  “See and Treat” approaches, which would improve compliance to pre cancer treatment  with the current HIV testing and counseling centers  in the country


References

 

1.Bruni L, Barrionuevo-Rosas L, Albero G, Aldea M, Serrano B, Valencia S, et al. ICO Information Centre on HPV and Cancer (HPV Information Centre). Human papillomavirus and related diseases in India. Summary report 2015-12-23. Available from: http://www.who.int/hpvcentre, accessed on January 21, 2016.

2. Annual Report 2013-14. New Delhi: Department of AIDS Control, National AIDS Control Organization, Ministry of Health and Family Welfare, Government of India; 2014.