Abstract
Pancreatic cancer (PC) is a highly lethal malignancy, and therapeutic advances over the last decade have translated into a survival benefit that can at best be characterized as modest. Approximately 53,670 people develop exocrine PC each year in the United States, and almost all are expected to die from the disease [1]. PC is expected to become the second leading cause of cancer-related mortality in the United States, second only to lung cancer in the next decade [1]. In the absence of validated predictive biomarkers to guide selection of therapy, clinical trial design in PC, over the last several decades, has defaulted to an “all-comers” approach. In clinical practice, it is well known that the inherent biology and response to treatment can be quite varied among patients with PC, arguing for their phenotypic/genotypic characterization, and biomarker-enriched treatment strategies.
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George, B. (2019). Molecular Profiling in Pancreatic Ductal Adenocarcinoma. In: Tsai, S., Ritch, P., Erickson, B., Evans, D. (eds) Management of Localized Pancreatic Cancer . Springer, Cham. https://doi.org/10.1007/978-3-319-98944-0_12
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DOI: https://doi.org/10.1007/978-3-319-98944-0_12
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