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Serum CA 19-9 Response to Neoadjuvant Therapy is Associated with Outcome in Pancreatic Adenocarcinoma

Background Baseline carbohydrate antigen 19-9 (CA 19-9) is a useful prognostic marker in pancreatic ductal adenocarcinoma (PDA); however, data on the significance of a change in CA 19-9 following neoadjuvant therapy are lacking. Methods All patients receiving neoadjuvant therapy for PDA from July 20...

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Bibliographic Details
Published in:Annals of surgical oncology 2014-12, Vol.21 (13), p.4351-4358
Main Authors: Boone, Brian A., Steve, Jennifer, Zenati, Mazen S., Hogg, Melissa E., Singhi, Aatur D., Bartlett, David L., Zureikat, Amer H., Bahary, Nathan, Zeh, Herbert J.
Format: Article
Language:English
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Summary:Background Baseline carbohydrate antigen 19-9 (CA 19-9) is a useful prognostic marker in pancreatic ductal adenocarcinoma (PDA); however, data on the significance of a change in CA 19-9 following neoadjuvant therapy are lacking. Methods All patients receiving neoadjuvant therapy for PDA from July 2010 to February 2013 were retrospectively reviewed. Resection rate, R0 resection rate, need for venous resection, and overall survival were correlated to CA 19-9 response. Fisher’s exact test, Kaplan–Meier survival analysis, and multivariate analysis using Cox regression were used. Results A total of 78 patients were studied (21 patients with resectable disease, 40 borderline resectable, and 17 with locally advanced disease). A variety of chemotherapies ± radiation were utilized during the study period. Overall, 56 patients (72 %) had a decrease in CA 19-9 of >50 % with neoadjuvant treatment. In borderline resectable patients, CA 19-9 response of >50 % predicted R0 resection (odds ratio 4.2; p  = 0.05). In borderline resectable patients who had an increase in CA 19-9, none of five (0 %) underwent R0 resection compared with 80 % of the remaining cohort ( p  = 0.001). The complete pathologic response rate was 29 % in patients who had a CA 19-9 response of >90 % versus 0 % in the remaining patients ( p  50 % resulted in improved overall survival (28.0 vs. 11.1 months; p  
ISSN:1068-9265
1534-4681
DOI:10.1245/s10434-014-3842-z