Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Feb;32(1):31-8.
doi: 10.1007/s00345-013-1033-3. Epub 2013 Feb 12.

Targeted therapy in renal cell carcinoma: moving from molecular agents to specific immunotherapy

Affiliations
Review

Targeted therapy in renal cell carcinoma: moving from molecular agents to specific immunotherapy

Jens Bedke et al. World J Urol. 2014 Feb.

Abstract

Non-specific immunotherapy has been for a long time a standard treatment option for patients with metastatic renal cell carcinoma but was redeemed by specific targeted molecular therapies, namely the VEGF and mTOR inhibitors. After moving treatment for mRCC to specific molecular agents with a well-defined mode of action, immunotherapy still needs this further development to increase its accuracy. Nowadays, an evolution from a rather non-specific cytokine treatment to sophisticated targeted approaches in specific immunotherapy led to a re-launch of immunotherapy in clinical studies. Recent steps in the development of immunotherapy strategies are discussed in this review with a special focus on peptide vaccination which aims at a tumor targeting by specific T lymphocytes. In addition, different combinatory strategies with immunomodulating agents like cyclophosphamide or sunitinib are outlined, and the effects of immune checkpoint modulators as anti-CTLA-4 or PD-1 antibodies are discussed.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
a Presentation of tumor-associated antigens. b Specific T-cell activation. c Immune checkpoints in RCC

Similar articles

Cited by

  • Toxicity mechanism-based prodrugs: glutathione-dependent bioactivation as a strategy for anticancer prodrug design.
    Zhang XY, Elfarra AA. Zhang XY, et al. Expert Opin Drug Discov. 2018 Sep;13(9):815-824. doi: 10.1080/17460441.2018.1508207. Epub 2018 Aug 13. Expert Opin Drug Discov. 2018. PMID: 30101640 Free PMC article. Review.
  • Systemic therapy in metastatic renal cell carcinoma.
    Bedke J, Gauler T, Grünwald V, Hegele A, Herrmann E, Hinz S, Janssen J, Schmitz S, Schostak M, Tesch H, Zastrow S, Miller K. Bedke J, et al. World J Urol. 2017 Feb;35(2):179-188. doi: 10.1007/s00345-016-1868-5. Epub 2016 Jun 9. World J Urol. 2017. PMID: 27277600 Free PMC article. Review.
  • Specific immunotherapy in renal cancer: a systematic review.
    Hirbod-Mobarakeh A, Gordan HA, Zahiri Z, Mirshahvalad M, Hosseinverdi S, Rini BI, Rezaei N. Hirbod-Mobarakeh A, et al. Ther Adv Urol. 2017 Feb;9(2):45-58. doi: 10.1177/1756287216681246. Epub 2016 Dec 19. Ther Adv Urol. 2017. PMID: 28203287 Free PMC article. Review.
  • Tumour and patient factors in renal cell carcinoma-towards personalized therapy.
    Haddad AQ, Margulis V. Haddad AQ, et al. Nat Rev Urol. 2015 May;12(5):253-62. doi: 10.1038/nrurol.2015.71. Epub 2015 Apr 14. Nat Rev Urol. 2015. PMID: 25868564 Review.
  • A neoantigen vaccine generates antitumour immunity in renal cell carcinoma.
    Braun DA, Moranzoni G, Chea V, McGregor BA, Blass E, Tu CR, Vanasse AP, Forman C, Forman J, Afeyan AB, Schindler NR, Liu Y, Li S, Southard J, Chang SL, Hirsch MS, LeBoeuf NR, Olive O, Mehndiratta A, Greenslade H, Shetty K, Klaeger S, Sarkizova S, Pedersen CB, Mossanen M, Carulli I, Tarren A, Duke-Cohan J, Howard AA, Iorgulescu JB, Shim B, Simon JM, Signoretti S, Aster JC, Elagina L, Carr SA, Leshchiner I, Getz G, Gabriel S, Hacohen N, Olsen LR, Oliveira G, Neuberg DS, Livak KJ, Shukla SA, Fritsch EF, Wu CJ, Keskin DB, Ott PA, Choueiri TK. Braun DA, et al. Nature. 2025 Mar;639(8054):474-482. doi: 10.1038/s41586-024-08507-5. Epub 2025 Feb 5. Nature. 2025. PMID: 39910301 Free PMC article. Clinical Trial.

References

    1. Lokich J. Spontaneous regression of metastatic renal cancer. Case report and literature review. Am J Clin Oncol. 1997;20:416–418. doi: 10.1097/00000421-199708000-00020. - DOI - PubMed
    1. Dengjel J, et al. Unexpected abundance of HLA class II presented peptides in primary renal cell carcinomas. Clin Cancer Res. 2006;12:4163–4170. doi: 10.1158/1078-0432.CCR-05-2470. - DOI - PubMed
    1. Saenz-Lopez P, et al. Higher HLA class I expression in renal cell carcinoma than in autologous normal tissue. Tissue Antigens. 2010;75:110–118. doi: 10.1111/j.1399-0039.2009.01409.x. - DOI - PubMed
    1. Attig S, et al. Simultaneous infiltration of polyfunctional effector and suppressor T cells into renal cell carcinomas. Cancer Res. 2009;69:8412–8419. doi: 10.1158/0008-5472.CAN-09-0852. - DOI - PubMed
    1. Schendel DJ, et al. Tumor-specific lysis of human renal cell carcinomas by tumor-infiltrating lymphocytes. I. HLA-A2-restricted recognition of autologous and allogeneic tumor lines. J Immunol. 1993;151:4209–4220. - PubMed

Publication types

MeSH terms

Substances