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A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Novel immunotherapy in metastatic renal cell carcinoma
Yang Hyun Cho1, Myung Soo Kim1, Ho Seok Chung1
1Department of Urology, Chonnam National University Medical School, Gwangju, Korea.
Abstract:
Despite the rapid development of therapeutic modalities for metastatic renal cell carcinoma (mRCC) over the past decade to include a number of targeted antiangiogenic therapies and traditional immunotherapy, such as high-dose interleukin-2 and interferon-α, mRCC continues to be associated with poor prognosis. Currently, several novel immunotherapy agents, such as cancer vaccines, adoptive cell therapy, and checkpoint inhibitors, such as programmed cell death-1 (PD-1 present on T cells), one of its ligands (PD-L1 present on antigen-presenting cells and tumor cells), and cytotoxic T-lymphocyte-associated protein-4 pathways, are being studied in mRCC and are showing promise as important steps in the management of this disease. This review summarizes the current landscape of standard and emerging immune therapeutics and other modalities for mRCC.
Insights
Metastatic renal cell carcinoma (mRCC) has a poor prognosis despite current therapies. Emerging immunotherapies, including checkpoint inhibitors, show promise for improving mRCC treatment outcomes.
Area of Science:
- Oncology
- Immunology
- Nephrology
Background:
- Metastatic renal cell carcinoma (mRCC) remains a challenging cancer with a poor prognosis.
- Standard treatments include targeted antiangiogenic therapies and traditional immunotherapies like interleukin-2 and interferon-α.
Purpose of the Study:
- To review the current landscape of standard and emerging immune therapeutics for mRCC.
- To highlight promising novel immunotherapy agents and other modalities in development.
Main Methods:
- Literature review of standard and emerging treatments for mRCC.
- Summary of current research on novel immunotherapies such as cancer vaccines, adoptive cell therapy, and checkpoint inhibitors.
Main Results:
- Despite advances, mRCC prognosis remains poor.
- Novel immunotherapies, including programmed cell death-1 (PD-1) and cytotoxic T-lymphocyte-associated protein-4 (CTLA-4) pathway inhibitors, are showing promise.
- Emerging agents represent important steps in managing mRCC.
Conclusions:
- Current standard therapies for mRCC have limitations in improving patient outcomes.
- Novel immunotherapies offer significant potential for advancing mRCC treatment.
- Further research into immune-based strategies is crucial for improving mRCC management.
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