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Reprogramming Pancreatic Ductal Adenocarcinoma to Pluripotency
Published on: February 2, 2024
Defining new paradigms for the treatment of pancreatic cancer
Khaldoun Almhanna1, Philip A Philip
1Department of Gastrointestinal Oncolgy, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Abstract:
Pancreatic cancer (PC) is the fourth leading cause of cancer death in the United States. Despite significant improvement in understanding disease biology, the 5-year survival rates remain less than 5%. Targeted agents failed to add any meaningful survival benefit in this patient population despite very promising pre-clinical data. The new paradigm for the treatment of PC must emphasize validation of targeted agents in the appropriate pre-clinical models, identification of predictive markers for disease response, and extending range of targets into cancer stem cells and tumor microenvironment. It is also necessary to perform studies that are designed to address the various stages of disease with respect to study endpoints and application of a multimodality approach in management. Phase III trials should only be considered when a strong efficacy signal is demonstrated in phase II studies that is based on a survival endpoint. This review will focus on the development of novel treatments in pancreas cancer and the proposed design of future clinical trials.
Insights
Pancreatic cancer treatment needs new strategies. Future research must validate targeted agents, identify biomarkers, and explore novel targets like cancer stem cells for better survival outcomes.
Area of Science:
- Oncology
- Cancer Research
- Translational Medicine
Background:
- Pancreatic cancer (PC) is a leading cause of cancer death in the US, with a 5-year survival rate below 5%.
- Current targeted therapies have not significantly improved survival despite promising preclinical data.
- A new treatment paradigm is urgently needed for pancreatic cancer.
Purpose of the Study:
- To review the development of novel treatments for pancreatic cancer.
- To propose designs for future clinical trials.
- To highlight the need for improved preclinical validation and identification of predictive markers.
Main Methods:
- Review of current literature on pancreatic cancer treatment.
- Analysis of challenges in targeted therapy development.
- Discussion of strategies for future clinical trial design.
Main Results:
- Targeted agents require rigorous validation in appropriate preclinical models.
- Identification of predictive markers is crucial for patient selection.
- Expanding therapeutic targets to include cancer stem cells and the tumor microenvironment is essential.
Conclusions:
- Future pancreatic cancer treatment strategies must incorporate validated targeted agents, predictive biomarkers, and novel targets.
- Clinical trial designs should address different disease stages and utilize multimodality approaches.
- Phase III trials should be initiated only after demonstrating strong efficacy signals in Phase II studies based on survival endpoints.
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