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1.
Dig Dis Sci ; 51(12): 2213-9, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17080251

ABSTRACT

Since significant neoplasia after initial colonoscopy is low, we conducted this pilot study to compare the predictive role for colorectal neoplasia recurrence of anti-DCC with that of Adnab-9 binding to colonic effluent of high-risk patients. DCC and Adnab-9 effluent ELISA were performed at baseline colonoscopies. The results of follow-up colonoscopies were reviewed. To ensure specificity, immunohistochemistry and Western blot was performed with anti-DCC and for Adnab-9 where optimal fixation times were also evaluated. Mean follow-up was 2.6 years. Of 21 patients, 6 of 10 who progressed to CRN and 2 of 11 who did not had a positive Adnab-9 ELISA result (P=0.08). Despite an initial good correlation with Adnab-9 ELISA results in a smaller dataset, we were unable to obtain consistent subsequent DCC immunohistochemistry or Western blot data using antibody from two different sources. However, the original dataset of Adnab-9 results was reproducible on repetition of the ELISA with a larger set of samples that included this initial dataset and optimal fixation time was 20 min. We conclude that Adnab-9 appears to be a promising prognostic marker for neoplasia in the high-risk population. Industry standards need to be developed for DCC monoclonal antibodies that may have similar utility.


Subject(s)
Adenoma/diagnosis , Adenoma/metabolism , Antigens, Tumor-Associated, Carbohydrate/metabolism , Colorectal Neoplasms/diagnosis , Colorectal Neoplasms/metabolism , Receptors, Cell Surface/metabolism , Tumor Suppressor Proteins/metabolism , Adenoma/genetics , Aged , Antibodies, Monoclonal/immunology , Antibodies, Monoclonal/metabolism , Antigens, Tumor-Associated, Carbohydrate/genetics , Antigens, Tumor-Associated, Carbohydrate/immunology , Biomarkers, Tumor/genetics , Biomarkers, Tumor/immunology , Biomarkers, Tumor/metabolism , Colonoscopy , Colorectal Neoplasms/genetics , DCC Receptor , Disease Progression , Enzyme-Linked Immunosorbent Assay , Humans , Male , Middle Aged , Neoplasm Recurrence, Local/diagnosis , Neoplasm Recurrence, Local/immunology , Neoplasm Recurrence, Local/metabolism , Pilot Projects , Predictive Value of Tests , Receptors, Cell Surface/genetics , Receptors, Cell Surface/immunology , Retrospective Studies , Sensitivity and Specificity , Tumor Suppressor Proteins/genetics , Tumor Suppressor Proteins/immunology
2.
Clin Gastroenterol Hepatol ; 2(3): 246-51, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15017609

ABSTRACT

BACKGROUND & AIMS: Distal colonic adenomas found on flexible sigmoidoscopy are associated with proximal neoplasias, thus requiring a complete colonoscopic examination, but data regarding the association of distal mixed polyps with proximal neoplasia are lacking. We conducted this study to elucidate the significance of distal mixed colonic polyps in predicting proximal neoplasia. METHODS: We retrospectively analyzed data from patients who underwent a flexible sigmoidoscopic examination for colorectal cancer screening and a follow-up colonoscopic examination because of distal colonic polyps. Distal index polyps were classified by a pathologist as early tubular adenoma (ETA), serrated, or true mixed categories. Index polyps also were immunostained with a monoclonal antibody, Adnab-9, a marker for the colorectal adenoma carcinoma sequence. RESULTS: In 636 patients with distal index polyps, 6% were malignant, 55% were adenomas, 13% were ETAs, 6% were serrated, 4% were true mixed, and 17% were hyperplastic. Compared with distal hyperplastic index polyps, distal malignant polyps (P = 0.0006) and adenomas (P = 0.001) were associated with a significantly increased number of synchronous proximal neoplasia, but the small distal mixed, serrated, or ETA did not predict the increased incidence of proximal neoplasia. Large distal polyps of each category were significantly associated with an increased number of synchronous proximal neoplasias. In support of these findings, immunostaining of distal polyps with Adnab-9 showed predictability for proximal neoplasia only in the adenoma category (P < 0.05). CONCLUSIONS: Small ETAs, serrated, or mixed polyps found on flexible sigmoidoscopic examination do not increase the probability of synchronous proximal neoplasia.


Subject(s)
Adenomatous Polyps/pathology , Colonic Neoplasms/pathology , Colonic Polyps/pathology , Precancerous Conditions/pathology , Adenomatous Polyps/epidemiology , Aged , Biopsy, Needle , Cohort Studies , Colonic Neoplasms/epidemiology , Colonic Polyps/epidemiology , Confidence Intervals , Female , Fiber Optic Technology , Humans , Immunohistochemistry , Male , Mass Screening , Middle Aged , Neoplasm Staging , Odds Ratio , Predictive Value of Tests , Probability , Risk Assessment , Sex Distribution , Sigmoidoscopes , Sigmoidoscopy/methods
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