Therefore, the principal aim of this study was to determine the utility of sIgG4 in distinguishing IAC from CCA. The following questions were addressed: (1) Is the sIgG4 level discriminatory

between IAC and CCA? (2) At what sIgG4 value can IAC be reliably distinguished from CCA (without the benefit or harm of an invasive histologic diagnosis)? (3) Is the ability of the sIgG4 to distinguish IAC from CCA affected by the concomitant existence of PSC? To answer these questions, we (1) compared sIgG4 levels in a test cohort of 126 patients with CCA BIBW2992 in vitro and 50 patients with IAC as well as in a validation cohort of 161 patients with CCA and 47 patients with IAC; (2) compared the demographic and serologic characteristics of patients with CCA without PSC (CCA-PSC), CCA with concomitant PSC (CCA+PSC), and IAC; and (3) examined whether there is an sIgG4 threshold at which CCA (with or without PSC) could be distinguished Neratinib from IAC with relatively high specificity and sensitivity. The secondary aim of this study was to determine the clinical significance of sIgG4 in CCA. The relationship between sIgG4 and CA19-9 levels and the association of sIgG4 with survival of CCA patients were investigated in both cohorts. AIP, autoimmune

pancreatitis; CCA, cholangiocarcinoma; CCA+PSC, CCA with concomitant PSC; CCA-PSC, CCA without PSC; HCC, hepatocellular carcinoma; IAC, IgG4-associated cholangitis; ISD, IgG4-related systemic disease; PSC, primary sclerosing cholangitis. The protocol for this study MCE公司 was approved by the Mayo Clinic Institutional Review Board. Patients referred to the Mayo Clinic Hepatobiliary Neoplasia Clinic between March 2003 and February 2011 and subsequently diagnosed with CCA were included (Fig. 1). A total of 287 CCA patients were divided into two separate cohorts. The test cohort included 126 CCA patients enrolled between March 2003 and June 2006. An additional 161 CCA patients enrolled between July 2006 and February 2011 served as a validation cohort.

The diagnosis of CCA was determined by histology, standard imaging criteria, or clinical course. The final diagnosis, age, gender, and clinical presentation, diagnosis and last follow-up dates, status at the last follow-up visit, serum IgG4 and CA 19-9 levels were abstracted from the clinical record. A total of 97 patients with AIC, as determined by the HISORt criteria, came from a prospective database of ISD cases maintained at Mayo Clinic, Rochester.12 Of these, 50 patients who were seen at the Mayo Clinic between January 1989 and October 2006 were included in the test cohort. At the time of last follow-up in March 2011, the 50 IAC patients in the test cohort had been followed-up for a median duration of 53.6 months (range, 11.5-265.9 months) after initial presentation and a median duration of 47.5 months (range, 1.5-84.9 months) after initiation of treatment. None of the IAC patients in the test cohort developed clinical evidence of CCA during follow-up.