Main Article Content
Abstract
Pancreatic cancer stands as one of the most daunting challenges in oncology, characterized by high mortality rates and limited progress in treatment outcomes over decades. A critical barrier to improving survival lies in the difficulty of early detection and prevention: symptoms often do not manifest until the disease has reached an advanced stage and reliable screening methods are lacking. This delayed diagnosis contributes significantly to the poor prognosis associated with pancreatic cancer. Genetically, pancreatic tumors exhibit a limited repertoire of frequently mutated genes, including KRAS, CDKN2A (p16), TP53, and SMAD4. Neoadjuvant therapies are being explored to downstage tumors and increase the likelihood of successful surgery. Despite advancements in treatment strategies, including novel drug combinations and multimodal approaches, disease recurrence following surgery remains common, highlighting the urgent need for innovative therapeutic approaches. We summarize the existing knowledge on the critical pathophysiological, molecular, translational, and clinical aspects of pancreatic cancer. Additionally, we outline potential future directions for research and patient management in this challenging disease.
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References
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