| Literature DB >> 26798437 |
Mariacristina Di Marco1, Elisa Grassi1, Sandra Durante1, Silvia Vecchiarelli1, Andrea Palloni1, Marina Macchini1, Riccardo Casadei1, Claudio Ricci1, Riccardo Panzacchi1, Donatella Santini1, Guido Biasco1.
Abstract
Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies with a five-year survival rate of approximately 5%. Several target agents have been tested in PDAC, but almost all have failed to demonstrate efficacy in late phase clinical trials, despite the better understanding of PDAC molecular biology generated by large cancer sequencing initiatives in the past decade. Eroltinib (a small-molecule tyrosine-kinase inhibitor of epidermal growth factor receptor) plus gemcitabine is the only schedule with a biological agent approved for advanced pancreatic cancer, but it has resulted in a very modest survival benefit in unselected patients. In our work, we report a summary of the main clinical trials (closed and ongoing) that refer to biological therapy evaluation in pancreatic cancer treatment.Entities:
Keywords: Antiangiogenic therapies; Embryonic pathway inhibitors; Epidermal growth factor receptor inhibitors; Molecular characterization; Pancreatic cancer; Targeted therapy
Year: 2016 PMID: 26798437 PMCID: PMC4714146 DOI: 10.4251/wjgo.v8.i1.55
Source DB: PubMed Journal: World J Gastrointest Oncol