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Checkpoint inhibitors in the treatment of urological malignancies
Lazar S Popovic1,2, Gorana Matovina-Brko1,2, Maja Popovic1,2
1Department of Medical Oncology, Oncology Institute of Vojvodina, Sremska Kamenica, Serbia.
Abstract:
Checkpoint inhibitors are monoclonal antibodies attach to several different receptors on T-cells or tumour cells expressing receptors for cytotoxic T-lymphocyte antigen 4 (CTLA-4), programmed death-1 (PD-1) and their ligand (PD-L1). Since 2010, numerous trials on different tumour types have been conducted, which was resulted in these drugs being approved for the treatment of melanoma, lung cancer, Hodgkin's lymphoma and head and neck cancers. Urological cancers, especially urothelial and renal-cell carcinomas, are immunogenic tumours. Since the late 70s, the bacillus Calmette-Gurin (BCG) vaccine has been used for intravesical instillation in non-muscle invasive bladder cancer from the mid-90s up until the discovery of tyrosine kinase inhibitors (TKIs) in 2007, interleukin-2 (IL-2) and interferon alpha (IFNα), which were the standard of care for metastatic renal-cell cancer. Two checkpoint inhibitors are already approved by the Food and Drug Administration: atezolizumab for metastatic urothelial cancer and nivolumab for metastatic renal-cell carcinoma. There are many drugs are in different phases of clinical development. Here we review the current status of checkpoint inhibitors in the treatment of urological tumours.
Insights
Checkpoint inhibitors, targeting CTLA-4, PD-1, and PD-L1, are revolutionizing cancer treatment. This review focuses on their current use and development for urological tumors like bladder and kidney cancers.
Area of Science:
- Immunology
- Oncology
- Pharmacology
Background:
- Checkpoint inhibitors are monoclonal antibodies targeting T-cell or tumor cell receptors like CTLA-4, PD-1, and PD-L1.
- Approved for melanoma, lung, and other cancers since 2010, they represent a significant advancement in cancer therapy.
- Urological cancers, including urothelial and renal-cell carcinomas, are immunogenic, suggesting potential efficacy for immunotherapy.
Purpose of the Study:
- To review the current status and clinical development of checkpoint inhibitors in treating urological tumors.
- To highlight the approved agents and ongoing research in this field.
Main Methods:
- Review of clinical trials and literature on checkpoint inhibitors in urological cancers.
- Analysis of approved drugs and drugs in clinical development phases.
Main Results:
- Two checkpoint inhibitors, atezolizumab and nivolumab, are FDA-approved for metastatic urothelial cancer and metastatic renal-cell carcinoma, respectively.
- Numerous other checkpoint inhibitors are in various stages of clinical development for urological malignancies.
Conclusions:
- Checkpoint inhibitors demonstrate significant promise and are increasingly utilized in the treatment of urological cancers.
- Ongoing research and development are expanding the therapeutic landscape for these immunogenic tumors.
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