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Role of vaccine therapy for renal cell carcinoma in the era of targeted therapy

Journal

INTERNATIONAL JOURNAL OF UROLOGY
Volume 20, Issue 8, Pages 744-755

Publisher

WILEY
DOI: 10.1111/iju.12147

Keywords

autologous tumor cell vaccine; dendritic cell vaccine; genetically modified vaccine; peptide vaccine; renal cell carcinoma

Funding

  1. Grants-in-Aid for Scientific Research [25293336] Funding Source: KAKEN

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Renal cell carcinoma is the most common malignant tumor originating from the kidney. Compared with other solid tumors, it does not respond to traditional management modalities, such as chemotherapy and radiotherapy. However, it is well known that renal cell carcinoma represents one of the most immune-responsive cancers and several immunotherapeutic strategies have been investigated in the management of renal cell carcinoma with variable degrees of success. The development of immunotherapy with a-interferon or high-dose interleukin-2 is the best established treatment, and is associated with durable disease control. Although the lack of defined antigens in renal cell carcinoma has hindered more specific vaccine development, research regarding vaccination therapy has been of special interest for the treatment of renal cell carcinoma for more than 30 years. At present, there are three types of cell-based vaccines in renal cell carcinoma treatment: autologous tumor-cell vaccines, genetically modified tumor vaccines and dendritic cell-based vaccines. A further type is peptide-based vaccination with tumor-associated antigens as possible targets, such as carbonic anhydrase IX, survivin and telomerase that are overexpressed in renal cell carcinoma. In the present article, we review data from completed clinical trials of vaccine therapy, and discuss future trials to assess the current knowledge and future role of vaccine therapy for renal cell carcinoma in the era of recently developed targeted therapy.

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