Carbonic anhydrase IX and human papillomavirus as diagnostic biomarkers of cervical dysplasia/neoplasia in women with a cytologic diagnosis of atypical glandular cells: a Gynecologic Oncology Group study in United States.

TitleCarbonic anhydrase IX and human papillomavirus as diagnostic biomarkers of cervical dysplasia/neoplasia in women with a cytologic diagnosis of atypical glandular cells: a Gynecologic Oncology Group study in United States.
Publication TypeJournal Article
Year of Publication2009
AuthorsLiao S-Y, Rodgers WH, Kauderer J, Bonfiglio TA, Walker JL, Darcy KM, Carter R, Hatae M, Levine L, Spirtos NM, Stanbridge EJ
JournalInt J Cancer
Volume125
Issue10
Pagination2434-40
Date Published2009 Nov 15
ISSN1097-0215
KeywordsAdenocarcinoma, Adult, Aged, Aged, 80 and over, Antigens, Neoplasm, Biomarkers, Tumor, Carbonic Anhydrase IX, Carbonic Anhydrases, Carcinoma, Squamous Cell, Cervical Intraepithelial Neoplasia, Cytodiagnosis, DNA, Viral, Female, Genotype, Humans, Immunoenzyme Techniques, Middle Aged, Neoplasm Invasiveness, Neoplasm Staging, Neoplasms, Glandular and Epithelial, Papanicolaou Test, Papillomaviridae, Papillomavirus Infections, Polymerase Chain Reaction, Retrospective Studies, Risk Factors, Sensitivity and Specificity, Uterine Cervical Neoplasms, Vaginal Smears, Young Adult
Abstract

High-risk human papillomavirus (H-HPV) infection is strongly linked to cervical neoplasia, but its role in detecting glandular lesions (GLs) is unclear. In the cervix, carbonic anhydrase IX (CA-IX) is expressed in cervical neoplasia, but rarely in the benign cervix. The diagnostic utility of these biomarkers was evaluated in women with a cytologic diagnosis of atypical glandular cells (AGC). H-HPV was detected using hybrid capture 2 (HC2) in liquid-based cytology, and CA-IX immunoreactivity was studied on conventional Pap smears. Of 403 patients, 111 (28%) were positive for significant cervical lesions (SCLs) including CIN2, CIN3, adenocarcinoma in situ or invasive carcinoma. CA-IX testing alone (n = 403) had a sensitivity of 75, 95 or 65% for SCLs, significant GLs or squamous lesions (SLs), respectively, with a specificity of 88% and a false negative rate (FNR defined as 1 minus negative predictive value) of 10%. Testing for H-HPV (n = 122) had a sensitivity of 97, 100 or 96% for SCLs, GLs or SLs, respectively, with a specificity of 87% and a FNR of 1%. The combination of CA-IX and H-HPV testing (n = 122), collectively, had the same sensitivity, specificity and FNR for SCLs, GLs or SLs as H-HPV testing alone. The conclusions of our study are that both H-HPV and CA-IX testing are useful diagnostic markers for GLs. However, H-HPV testing is a better diagnostic marker for SLs. The combination of CA-IX with H-HPV testing does not improve the diagnostic accuracy for cervical neoplasia in women with AGC diagnosis over that of H-HPV testing alone.

DOI10.1002/ijc.24615
Alternate JournalInt J Cancer
PubMed ID19670419
PubMed Central IDPMC2779726
Grant ListU10 CA037517 / CA / NCI NIH HHS / United States
CA 37517 / CA / NCI NIH HHS / United States
CA 11479 / CA / NCI NIH HHS / United States
CA 27469 / CA / NCI NIH HHS / United States
U10 CA027469 / CA / NCI NIH HHS / United States
U10 CA037517-25 / CA / NCI NIH HHS / United States
U10 CA027469-29 / CA / NCI NIH HHS / United States
Related Faculty: 
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