The benefits of CCRT shown here should be validated in a randomized clinical trial. Conclusions In conclusion, our retrospective results strongly suggest that, until a randomized controlled clinical trial is reported, patients who have been treated with chemotherapy alone with no progression may benefit from the addition of chemoradiation therapy if they can tolerate it. Providers should plan

to add chemoradiation therapy after a trial period of chemotherapy alone for any patient who doesn’t progress and can tolerate combined therapy. Treatment with CCRT is associated Inhibitors,research,lifescience,medical with improved median OS and MFS compared to chemotherapy alone. This is a strategy that selects for patients who are less likely to develop early metastases and therefore have a better prognosis. A prospective randomized study is needed to confirm these findings. Our analysis suggests that other factors that portend improved survival include younger age, borderline resectable disease, Inhibitors,research,lifescience,medical and margin-negative resection. Acknowledgements This data was presented as an oral presentation at the American Society for Radiation Oncology Annual Meeting, Oct 30, 2012. Disclosure: The authors declare no conflict of interest.
In this issue of the Journal of Gastrointestinal

Oncology De Angelis et al. provide a comprehensive review of the role of endoscopic ultrasound (EUS) in the Inhibitors,research,lifescience,medical management of selleck kinase inhibitor pancreatic cancer. At present the two main established roles of EUS are imaging and tissue acquisition. In addition some EUS-guided therapieshave gained limited but expanding role in pancreatic Inhibitors,research,lifescience,medical cancer patients. As correctly pointed by the authors, the role of standard EUS imaging for diagnosis and staging has decreased with the advent of dynamic contrast enhanced multi-detector row computed tomography (MDCT). Nevertheless, Inhibitors,research,lifescience,medical contrary to the prevailing perceptions both EUS and MDCT are operator dependent and significant variability of image quality and interpretations

exist with MDCT. Furthermore, EUS remains superior imaging (-)-p-Bromotetramisole Oxalate modality to detect small pancreatic lesions, mural nodules within a cyst, small lymph nodes and coexisting biliary pathology. We concur with the authors that inmost patients EUS and MDCT should be considered complimentary rather than competing imaging modalities for the evaluation of patients with suspected pancreatic lesions with MDCT been the initial test in most patients. Anotable exception is the screening of populations at high risk for pancreatic cancer where the recent International Cancer of the Pancreas Screening (CAPS) Consortium summit endorsed EUS as the initial test of choice (1,2). EUS is also preferably used for serial surveillance of premalignant pancreatic lesions [e.g., Intraductal papillary mucinous neoplasm (IPMN)] without the radiation exposure associated with MDCT (3).