Document Type : Research Articles
Consultant Pathologist and Research Scholar, Cancer Cell Biology Division, Department of Biotechnology, Manipur University, India.
District AIDS Control Officer, Tamenglong, India.
OB/GYN, JNIMS Jawaharlal Nehru Institute of Medical Sciences. India.
Background: Liquid based cytology with dual biomarkers has improved sensitivity and specificity in detecting
high grade cervical intraepithelial neoplasia (CIN). In low resource settings, especially in organized camps, LBC is
costly and immunohistochemistry on conventional pap smears is difficult to standardize with consumption of lots of
reagents. In present study, to improve the accuracy of conventional pap smears and reduce the cost of biomarker
testing, we evaluated conventional cell blocks (CCBs) preparations with biomarkers to detect high-grade CIN in
resource-poor organized screening programs. We also studied feasibility of using CCB as primary screening test.
Material and Methods: A total of 350 participants were included in the cross-sectional evaluation of the screening
tests. A conventional Papanicolaou (Pap) smear was obtained, and another sample was then collected and placed in
10% neutral buffered formalin for CB preparation. All abnormal Pap tests and CBs were stained for the biomarkers
p16INK4a and Ki67. Histopathology with p16INK4a expression was considered the gold standard. Diagnostic tests
were compared using MacNemar’s test and receiver operating curves were plotted. Results: The sensitivity, specificity,
and diagnostic accuracy of CCB cytology, CB + p16 cytology and CB + p16Ki67 cytology for detecting CIN2+ lesions
were 85.71%, 100%, 97.44%; 100%, 93.75%, 94.87%; and 85.71%, 100%, 97.44%, respectively. The Ki67 index
could further categorize low grade lesions into lesions with low proliferative index and with high proliferative index
(Pearson chi-square p value <0.001). Conclusion: If CB preparation is standardized, CCB cytology with biomarkers
can have better diagnostic accuracy than conventional cytology, can classify low grade lesions likely to progress and
can be used in field settings as primary screening test.