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Updated: Oct 2, 2025

Flow Cytometry-Based Isolation and Therapeutic Evaluation of Tumor-Infiltrating Lymphocytes in a Mouse Model of Pancreatic Cancer
Published on: January 17, 2025
The next wave of cellular immunotherapies in pancreatic cancer
Dannel Yeo1,2,3, Caroline Giardina2,4, Payal Saxena2,5
1Li Ka Shing Cell & Gene Therapy Program, The University of Sydney, Camperdown, NSW 2050, Australia.
Abstract:
Pancreatic cancer is an aggressive disease that is predicted to become the second leading cause of cancer-related death worldwide by 2030. The overall 5-year survival rate is around 10%. Pancreatic cancer typically presents late with locally advanced or metastatic disease, and there are limited effective treatments available. Cellular immunotherapy, such as chimeric antigen receptor (CAR) T cell therapy, has had significant success in treating hematological malignancies. However, CAR T cell therapy efficacy in pancreatic cancer has been limited. This review provides an overview of current and ongoing CAR T cell clinical studies of pancreatic cancer and the major challenges and strategies to improve CAR T cell efficacy. These strategies include arming CAR T cells; developing off-the-shelf allogeneic CAR T cells; using other immune CAR cells, like natural killer cells and tumor-infiltrating lymphocytes; and combination therapy. Careful incorporation of preclinical models will enhance management of affected individuals, assisting incorporation of cellular immunotherapies. A multifaceted, personalized approach involving cellular immunotherapy treatment is required to improve pancreatic cancer outcomes.
Insights
Chimeric antigen receptor (CAR) T-cell therapy shows promise for pancreatic cancer, but efficacy is limited. Strategies like arming CAR T-cells and combination therapies are being explored to improve outcomes for this aggressive disease.
Area of Science:
- Oncology
- Immunotherapy
- Cancer Research
Background:
- Pancreatic cancer is a highly aggressive malignancy with a poor prognosis and limited treatment options.
- Current 5-year survival rates for pancreatic cancer are approximately 10%, often due to late-stage diagnosis.
- Cellular immunotherapies, like CAR T-cell therapy, have shown success in other cancers but face challenges in pancreatic cancer.
Purpose of the Study:
- To review current and ongoing clinical studies of CAR T-cell therapy for pancreatic cancer.
- To identify major challenges hindering CAR T-cell efficacy in pancreatic cancer.
- To explore strategies aimed at improving CAR T-cell treatment outcomes for pancreatic cancer patients.
Main Methods:
- Review of existing literature on CAR T-cell therapy in pancreatic cancer.
- Analysis of ongoing clinical trials and their methodologies.
- Identification and categorization of proposed strategies to enhance CAR T-cell function.
Main Results:
- CAR T-cell therapy efficacy in pancreatic cancer remains limited compared to hematological malignancies.
- Several strategies are under investigation to overcome these limitations.
- Preclinical models are crucial for advancing cellular immunotherapy in pancreatic cancer.
Conclusions:
- Improving pancreatic cancer outcomes requires a multifaceted and personalized approach incorporating cellular immunotherapy.
- Strategies such as enhancing CAR T-cells, utilizing allogeneic CAR T-cells, exploring alternative immune cells (NK, TILs), and combination therapies are key.
- Further research and careful integration of preclinical findings are essential for successful clinical application.
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