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Updated: Jul 30, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Management of Advanced Prostate Cancer in the Precision Oncology Era
Claire M Gillette1, Gabriel A Yette1, Scott D Cramer1
1Department of Pharmacology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Abstract:
Prostate cancer (PC) is the second leading cause of cancer death in men in the United States. While diversified and improved treatment options for aggressive PC have improved patient outcomes, metastatic castration-resistant prostate cancer (mCRPC) remains incurable and an area of investigative therapeutic interest. This review will cover the seminal clinical data supporting the indication of new precision oncology-based therapeutics and explore their limitations, present utility, and potential in the treatment of PC. Systemic therapies for high-risk and advanced PC have experienced significant development over the past ten years. Biomarker-driven therapies have brought the field closer to the goal of being able to implement precision oncology therapy for every patient. The tumor agnostic approval of pembrolizumab (a PD-1 inhibitor) marked an important advancement in this direction. There are also several PARP inhibitors indicated for patients with DNA damage repair deficiencies. Additionally, theranostic agents for both imaging and treatment have further revolutionized the treatment landscape for PC and represent another advancement in precision medicine. Radiolabeled prostate-specific membrane antigen (PSMA) PET/CT is rapidly becoming a standard of care for diagnosis, and PSMA-targeted radioligand therapies have gained recent FDA approval for metastatic prostate cancer. These advances in precision-based oncology are detailed in this review.
Insights
Precision oncology advances, including biomarker-driven therapies like PD-1 inhibitors and PARP inhibitors, are revolutionizing prostate cancer (PC) treatment. PSMA-targeted theranostics offer new hope for metastatic castration-resistant prostate cancer (mCRPC).
Area of Science:
- Oncology
- Precision Medicine
- Radiopharmaceutical Therapy
Background:
- Prostate cancer (PC) is a leading cause of cancer death in men.
- Metastatic castration-resistant prostate cancer (mCRPC) remains incurable, necessitating novel therapeutic strategies.
- Recent advancements in systemic therapies and precision oncology offer new hope for patients with advanced PC.
Purpose of the Study:
- To review seminal clinical data supporting new precision oncology therapeutics for PC.
- To explore the limitations, utility, and potential of these novel treatments.
- To detail recent advances in biomarker-driven therapies and theranostics for PC.
Main Methods:
- Review of clinical data for precision oncology therapeutics in prostate cancer.
- Analysis of biomarker-driven therapies, including PD-1 inhibitors and PARP inhibitors.
- Evaluation of theranostic agents, such as PSMA-targeted radioligand therapies.
Main Results:
- Biomarker-driven therapies are bringing precision oncology closer to reality for all PC patients.
- Tumor-agnostic approval of pembrolizumab (PD-1 inhibitor) signifies a major step forward.
- PSMA-targeted theranostics are transforming PC diagnosis and treatment, with recent FDA approvals for mCRPC.
Conclusions:
- Precision-based oncology has significantly advanced the treatment landscape for prostate cancer.
- Theranostic agents and biomarker-driven therapies represent key innovations in managing advanced and metastatic PC.
- Continued research and application of these precision approaches hold promise for improving outcomes in PC.
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