Pancreatic ductal adenocarcinoma (PDAC) presents challenges in oncology due to limited therapeutic progress despite advancements in surgery, chemotherapy, and supportive care, leading to poor survival rates.
The dominant mutation in PDAC, KRAS oncogene, historically considered 'undruggable,' has hampered targeted therapy development; however, recent advancements like G12C inhibitors offer hope for precision treatments.
PDAC's immunosuppressive tumor microenvironment poses a significant hurdle to effective treatment, incentivizing approaches to reprogram the stroma and boost anti-tumor immune responses.
Research is exploring innovative immunotherapies, combination treatments, and immune modulation to enhance PDAC response, given the limitations of immune checkpoint inhibitors.
Early detection methods, including biomarkers, liquid biopsies, and advanced imaging, are crucial to improving PDAC outcomes by facilitating timely interventions and curative surgeries.
Adaptive trial structures and biomarker-driven enrollment criteria are being adopted to enhance the efficacy of clinical trials for PDAC treatment, addressing the disease's complexity and patient variability.
Barriers in PDAC care, such as limited awareness, healthcare disparities, and disease heterogeneity, underscore the need for comprehensive education, policy reforms, and multidisciplinary care teams.
Integrating supportive and palliative care early is vital due to the rapid clinical progression of PDAC, emphasizing personalized treatment approaches based on newly identified genetic subtypes.
Targeting metabolic pathways of PDAC cells and considering combination therapies to disrupt the tumor microenvironment and enhance treatment efficacy are emerging strategies in PDAC management.
Innovations in drug delivery technologies, including nanoparticle formulations and localized release systems, aim to overcome stromal barriers and improve drug concentrations within tumors, potentially enhancing patient outcomes.