Opinion - (2025) Volume 11, Issue 1
Received: 28-Jan-2025, Manuscript No. aso-25-165911;
Editor assigned: 30-Jan-2025, Pre QC No. P-165911;
Reviewed: 13-Feb-2025, QC No. Q-165911;
Revised: 20-Feb-2025, Manuscript No. R-165911;
Published:
27-Feb-2025
, DOI: 10.37421/2471-2671.2025.11.151
Citation: Fastro, Amir. “Immunotherapy for Prostate Cancer: Current Status and Future Perspectives.” Arch Surg Oncol 11 (2025): 151.
Copyright: © 2025 Fastro A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
The concept of immunotherapy in cancer treatment dates back several decades, but it has only recently gained significant attention due to the success of immune checkpoint inhibitors and other immunotherapeutic strategies in cancers like melanoma and non-small cell lung cancer. Immunotherapy works by enhancing the immune system's ability to recognize and attack cancer cells. One of the most well-known mechanisms in immunotherapy involves the inhibition of immune checkpoints, such as the programmed cell death protein 1 (PD-1) and its ligand (PD-L1), which cancer cells often exploit to evade immune surveillance. These immune checkpoints act as brakes on the immune system, preventing T cells from attacking cancer cells. By blocking these checkpoints, immunotherapies can restore T cell function and allow the immune system to mount a stronger response against tumors [2].
In prostate cancer, the potential for immunotherapy has generated considerable interest, especially given the disease's tendency to relapse after initial treatments and the limited long-term efficacy of existing therapies [3]. The most widely studied immunotherapy approach for prostate cancer is the use of immune checkpoint inhibitors. Despite the success of these inhibitors in other cancers, their effectiveness in prostate cancer has been modest. This is largely due to the relatively low mutational burden of prostate cancer compared to other malignancies, which means that prostate cancer cells may not produce as many neoantigens for the immune system to target. Additionally, prostate cancer cells have various mechanisms of immune evasion, such as low levels of antigen presentation and an immunosuppressive tumor microenvironment, which complicate the success of immunotherapy [4]. One of the immunotherapeutic agents that has been explored in prostate cancer is the immune checkpoint inhibitor pembrolizumab, an anti-PD-1 antibody. Clinical trials have shown that while pembrolizumab can be effective in a subset of prostate cancer patients, its overall response rate has been relatively low. In particular, patients with microsatellite instability or mismatch repair deficiency, which are rare in prostate cancer but associated with a higher mutational burden, tend to respond better to checkpoint inhibitors. These findings have led to the exploration of biomarkers that can predict which patients are more likely to benefit from immunotherapy, helping to identify those who may derive the most benefit from these treatments [5].
Google Scholar Cross Ref Indexed at
Google Scholar Cross Ref Indexed at
Google Scholar Cross Ref Indexed at
Google Scholar Cross Ref Indexed at
Google Scholar Cross Ref Indexed at
Archives of Surgical Oncology received 37 citations as per Google Scholar report