A significant benefit was demonstrated with the addition of chemotherapy to RT, but no benefit was seen with RT dose escalation. The median OS for patients in the moderate high dose chemo-RT arms were both approximately ten months (5). Profound technical advances in RT delivery have inspired an array of modern RT dose escalation series in unresectable Inhibitors,research,lifescience,medical PAC

using a variety of RT delivery methods (6,8,10-12,14). In some series median OS has remained comparable to that demonstrated by the GITSG trial nearly 25 years prior (8,14). The heterogeneous results from these trials have resulted in conflicting conclusions regarding the benefit of protocol radiosurgical dose escalation, with some series concluding that radiosurgical boost has no role in dose escalation for unresectable PAC (14). Still, more recent series have concluded that this technology is promising and warrants further

investigation (6,8,9). The question remains, Inhibitors,research,lifescience,medical despite the improvements in local control seen with dose escalation, what additional factors associated with these dose escalation trials could be contributing to only a minimal change in OS numbers? The most likely explanation is that patients treated with dose escalation have increased toxicity detrimental to OS or that poorly selected patients succumb to subsequent distant metastatic disease. There is room for tremendous speculation as to why RT dose escalation Inhibitors,research,lifescience,medical has failed thus far in unresectable PAC. As with any aggressive local therapy, patient selection remains selleck kinase inhibitor absolutely critical. The ability Inhibitors,research,lifescience,medical to select those patients that will not fail distantly after completing a course of aggressive local therapy is essential to translating local control improvements into meaningful OS improvements. Recently, great advancements in patient selection through both neoadjuvant chemotherapy and genetic

analysis have provided hope in this arena (3,4,16). Additionally, an often overlooked and understudied area of RT delivery in unresectable PAC is the modality of GTV delineation. Recently, retrospective data have Inhibitors,research,lifescience,medical emerged and called into question the volumes delineated on abdominal CT and MRI (17,18). When local tumors are treated alone with increasingly small margins, the process of a pancreatic tumor GTV delineation must be carefully studied before a minimal margin is used expanding GTV-PTV. The GTV delineation in this disease may have important implications for normal tissue toxicity Entinostat and local control, particularly in the setting of dose escalation. Despite the conflicting trials, hope remains for improved outcomes with RT dose escalation in unresectable PAC. In a series by Ben-Josef et al., high quality intensity modulated radiation therapy (IMRT) with strict dose constraints was delivered in a Time-to-Event Continual Reassessment (TITE-CRM) trial that accrued a total of 50 patients (19). The recommended dose was determined to be 55 Gy over 25 fractions, and 2-year OS was an encouraging 14.8 months (11).