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Updated: Feb 13, 2026

An Orthotopic Murine Model of Human Prostate Cancer Metastasis
Published on: September 18, 2013
Combining immune check-point blockade and cryoablation in an immunocompetent hormone sensitive murine model of
Benjamin Benzon1, Stephanie A Glavaris2, Brian W Simons2
1Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA. benzon.benjamin@gmail.com.
Background:
Prostate cancer remains the second leading cause of cancer related death in men. Immune check point blocking antibodies have revolutionized treatment of multiple solid tumors, but results in prostate cancer remain marginal. Previous reports have suggested that local therapies, in particular cryoablation might increase tumor immunogenicity. In this work, we examine potential synergism between tumor cryoabalation and check point blocking antibodies.
Methods:
FVB/NJ mice were injected subcutaneously into each flank with either 1 × 106 or 0.2 × 106 isogenic hormone sensitive Myc-Cap cells to establish synchronous grafts. Mice were treated with four intraperitoneal injections of anti-PD-1 (10 mg/kg), anti-CTLA-4 (1 mg/kg), or isotype control antibody with or without adjuvant cryoablation of the larger tumor graft and with or without neo-adjuvant androgen deprivation with degarelix (ADT). Mouse survival and growth rates of tumor grafts were measured. The immune dependency of observed oncological effects was evaluated by T cell depletion experiments.
Results:
Treatment with anti-CTLA-4 antibody and cryoablation delayed the growth of the distant tumor by 14.8 days (p = 0.0006) and decreased the mortality rate by factor of 4 (p = 0.0003) when compared to cryoablation alone. This synergy was found to be dependent on CD3+ and CD8+ cells. Combining PD-1 blockade with cryoablation did not show a benefit over use of either treatment alone. Addition of ADT to anti-PD1 therapy and cryoablation doubled the time to accelerated growth in the untreated tumors (p = 0.0021) and extended survival when compared to cryoablation combined with ADT in 25% of the mice. Effects of combining anti-PD1 with ADT and cryoablation on mouse survival were obviated by T cell depletion.
Conclusion:
Trimodal therapy consisting of androgen deprivation, cryoablation and PD-1 blockade, as well as the combination of cryoablation and low dose anti-CTLA-4 blockade showed that local therapies with cryoablation could be considered to augment the effects of checkpoint blockade in prostate cancer.
Insights
Combining cryoablation with anti-CTLA-4 antibody therapy shows promise for treating prostate cancer by delaying tumor growth and reducing mortality. This synergy is T cell-dependent, suggesting a role for immunotherapy in conjunction with local treatments.
Area of Science:
- Oncology
- Immunotherapy
- Surgical Oncology
Background:
- Prostate cancer is a leading cause of cancer death in men.
- Immune checkpoint inhibitors have limited efficacy in prostate cancer.
- Local therapies like cryoablation may enhance anti-tumor immunity.
Purpose of the Study:
- To investigate the synergistic effects of cryoablation and immune checkpoint blockade in prostate cancer.
- To evaluate the combination of cryoablation with anti-PD-1 and anti-CTLA-4 antibodies.
- To assess the impact of androgen deprivation therapy (ADT) in combination with cryoablation and checkpoint inhibitors.
Main Methods:
- Murine prostate cancer model (Myc-Cap cells) in FVB/NJ mice.
- Treatment with anti-PD-1, anti-CTLA-4 antibodies, cryoablation, and ADT (degarelix).
- Evaluation of tumor growth, survival rates, and immune dependency via T cell depletion.
Main Results:
- Anti-CTLA-4 antibody plus cryoablation significantly delayed distant tumor growth and reduced mortality compared to cryoablation alone (p<0.001).
- This combination's efficacy was dependent on CD3+ and CD8+ T cells.
- Adding ADT to anti-PD-1 and cryoablation improved tumor growth delay and survival, but effects were abrogated by T cell depletion.
Conclusions:
- Cryoablation can augment checkpoint blockade efficacy in prostate cancer.
- Combination of cryoablation with low-dose anti-CTLA-4 antibody shows significant therapeutic potential.
- Trimodal therapy (ADT, cryoablation, anti-PD-1) warrants further investigation for prostate cancer treatment.
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