Published online Jul 15, 2024. doi: 10.4251/wjgo.v16.i7.2902
Revised: April 4, 2024
Accepted: May 21, 2024
Published online: July 15, 2024
Processing time: 176 Days and 6.6 Hours
Pancreatic ductal adenocarcinoma (PDAC) presents significant challenges in patient management due to a dismal prognosis, increasing incidence, and limited treatment options. In this regard, precision medicine, which personalizes treatments based on tumour molecular characteristics, has gained great interest. However, its widespread implementation is not fully endorsed in current recommendations. This review explores key molecular alterations in PDAC, while emphasizing differences between KRAS-mutated and KRAS-wild-type tumours. It assesses the practical application of precision medicine in clinical settings and outlines potential future directions with respect to PDAC. Actionable molecular targets are examined with the aim of enhancing our understanding of PDAC molecular biology. Insights from this analysis may contribute to a more refined and personalized approach to pancreatic cancer treatment, ultimately improving patient outcomes.
Core Tip: Management of patients with pancreatic cancer (PDAC) is a real challenge due to a poor prognosis, a rising incidence and few therapeutic options. Precision medicine is an approach that seeks to personalize treatments to the specific molecular characteristics of individual tumors. Despite a growing interest in applying molecular precision medicine for PDAC management, large scale precision medicine is not endorsed so far by the last recommendations. We review the main actionable molecular alterations found in PDAC, highlighting the differences between KRAS-mutated and KRAS-wild-type tumors, as well as precision medicine in clinical practice and future directions for precision medicine in PDAC.