The future of cellular therapy for the treatment of renal cell carcinoma

Expert Opin Biol Ther. 2024 Nov;24(11):1245-1259. doi: 10.1080/14712598.2024.2418321. Epub 2024 Nov 4.

Abstract

Introduction: Systemic treatment options for renal cell carcinoma (RCC) have expanded considerably in recent years, and both tyrosine kinase inhibitors and immune checkpoint inhibitors, alone or in combination, have entered the clinical arena. Adoptive cell immunotherapies have recently revolutionized the treatment of cancer and hold the promise to further advance the treatment of RCC.

Areas covered: In this review, we summarize the latest preclinical and clinical development in the field of adoptive cell immunotherapy for the treatment of RCC, focusing on lymphokine-activated killer (LAK) cells, cytokine-induced killer (CIK) cells, tumor-infiltrating T cells (TILs), TCR-engineered T cells, chimeric antigen receptor (CAR) T cells, and dendritic cell vaccination strategies. Perspectives on emerging cellular products including CAR NK cells, CAR macrophages, as well as γδ T cells are also included.

Expert opinion: So far, areas of greater therapeutic success of adoptive cell therapies include the adjuvant administration of CIK cells and the transfer of anti-CD70 CAR T cells in patients with metastatic RCC. Bench to bedside and back research will be needed to overcome current limitations of adoptive cell therapies in RCC, primarily aiming at improving the safety of immune cell products, optimizing their antitumor activity and generating off-the-shelf products ready for clinical use.

Keywords: Adoptive cell therapy; CAR NK cells; CAR T cells; CIK cells; LAK cells; TCR-engineered T cells; TILs; kidney cancer.

Publication types

  • Review

MeSH terms

  • Animals
  • Carcinoma, Renal Cell* / immunology
  • Carcinoma, Renal Cell* / therapy
  • Humans
  • Immunotherapy, Adoptive* / adverse effects
  • Immunotherapy, Adoptive* / trends
  • Kidney Neoplasms* / immunology
  • Kidney Neoplasms* / pathology
  • Kidney Neoplasms* / therapy
  • Receptors, Chimeric Antigen / immunology

Substances

  • Receptors, Chimeric Antigen