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A Real-time Potency Assay for Chimeric Antigen Receptor T Cells Targeting Solid and Hematological Cancer Cells
Published on: November 12, 2019
Chimeric Antigen Receptor T-Cell Therapy in Metastatic Castrate-Resistant Prostate Cancer
Mahasha P J Perera1,2,3,4, Patrick B Thomas1,2,4, Gail P Risbridger5
1School of Biomedical Sciences at Translational Research Institute (TRI), Queensland University of Technology (QUT), Brisbane, QLD 4102, Australia.
Abstract:
Prostate cancer is the most commonly diagnosed solid-organ cancer amongst males worldwide. Metastatic castrate-resistant prostate cancer (mCRPC) is a rapidly fatal end-sequelae of prostate cancer. Therapeutic options for men with mCRPC are limited and are not curative in nature. The recent development of chimeric antigen receptor T-cell (CAR-T) therapy has revolutionised the treatment of treatment-resistant haematological malignancies, and several studies are underway investigating the utility of this technology in the treatment of solid tumours. In this review, we evaluate the current treatment options for men with mCRPC as well as the current landscape of preclinical and clinical trials of CAR-T cell therapy against prostate cancer. We also appraise the various prostate cancer-specific tumour-associated antigens that may be targeted by CAR-T cell technology. Finally, we examine the potential translational barriers of CAR-T cell therapy in solid tumours. Despite preclinical success, preliminary clinical trials in men with prostate cancer have had limited efficacy. Therefore, further clinically translatable preclinical models are required to enhance the understanding of the role of this investigational therapeutic in men with mCRPC. In the era of precision medicine, tailored immunotherapy administered to men in a tumour-agnostic approach provides hope to a group of men who otherwise have few treatment options available.
Insights
Chimeric antigen receptor T-cell (CAR-T) therapy shows promise for metastatic castrate-resistant prostate cancer (mCRPC). Further research is needed to overcome limited efficacy in clinical trials for this difficult-to-treat cancer.
Area of Science:
- Oncology
- Immunotherapy
- Cancer Research
Background:
- Prostate cancer is a leading cause of cancer death in men globally.
- Metastatic castrate-resistant prostate cancer (mCRPC) has limited therapeutic options.
- Chimeric antigen receptor T-cell (CAR-T) therapy has transformed hematological cancer treatment.
Purpose of the Study:
- To review current mCRPC treatments.
- To evaluate CAR-T cell therapy in prostate cancer preclinical and clinical trials.
- To identify prostate cancer antigens for CAR-T targeting and assess translational barriers.
Main Methods:
- Literature review of mCRPC treatments.
- Analysis of preclinical and clinical CAR-T therapy studies for prostate cancer.
- Appraisal of prostate cancer-specific antigens and CAR-T translational challenges.
Main Results:
- CAR-T therapy has shown preclinical success in prostate cancer models.
- Early clinical trials of CAR-T for prostate cancer have demonstrated limited efficacy.
- Identifying suitable tumor-associated antigens and overcoming solid tumor barriers are key.
Conclusions:
- CAR-T therapy holds potential for mCRPC treatment, offering hope in precision medicine.
- Enhanced preclinical models are crucial for improving CAR-T efficacy in solid tumors.
- Targeted immunotherapy represents a promising avenue for patients with limited options.
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