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First and Second-line Treatments in Metastatic Renal Cell Carcinoma.

Publication ,  Journal Article
Barragan-Carrillo, R; Saad, E; Saliby, R-M; Sun, M; Albiges, L; Bex, A; Heng, D; Mejean, A; Motzer, RJ; Plimack, ER; Powles, T; Rini, BI ...
Published in: Eur Urol
February 2025

BACKGROUND AND OBJECTIVE: The treatment landscape for metastatic renal cell carcinoma (mRCC) has evolved significantly in recent years, leading to improved outcomes. The aim of this review is to provide clinicians with a practical guide for selecting first- and second-line treatments on the basis of current evidence. METHODS: We critically evaluated systemic treatment strategies for mRCC. A comprehensive literature search was conducted in PubMed and Embase, alongside manual searches of guidelines and conference proceedings up to October 2024. A narrative review was performed to reach a consensus, with voting used to resolve differing opinions among authors. KEY FINDINGS AND LIMITATIONS: First-line treatment options include immune checkpoint inhibitor (ICI)-based combinations or tyrosine kinase inhibitors (TKIs). Four combination regimens have been approved internationally. Owing to the lack of head-to-head trials and standardized biomarkers, treatment decisions rely on factors such as International Metastatic RCC Database Consortium (IMDC) risk score, functional status, safety profiles, sarcomatoid features, use of immunosuppressive drugs, and need for immediate response. Despite advances, many patients will experience disease progression on ICI-based therapy, necessitating further treatment. The need for standardized second-line approaches remains unmet. TKIs, alone or with everolimus, show promising efficacy, while HIF2a inhibitors offer newer options with a favorable toxicity profile. Rechallenge with ICIs after early progression is not recommended. CONCLUSIONS AND CLINICAL IMPLICATIONS: For optimal mRCC treatment selection, clinicians must carefully balance efficacy, toxicity, and patient preferences, especially when transitioning between first- and second-line therapies, to provide individualized care.

Duke Scholars

Published In

Eur Urol

DOI

EISSN

1873-7560

Publication Date

February 2025

Volume

87

Issue

2

Start / End Page

143 / 154

Location

Switzerland

Related Subject Headings

  • Urology & Nephrology
  • Protein Kinase Inhibitors
  • Neoplasm Metastasis
  • Kidney Neoplasms
  • Immune Checkpoint Inhibitors
  • Humans
  • Carcinoma, Renal Cell
  • 3202 Clinical sciences
  • 1103 Clinical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Barragan-Carrillo, R., Saad, E., Saliby, R.-M., Sun, M., Albiges, L., Bex, A., … Choueiri, T. K. (2025). First and Second-line Treatments in Metastatic Renal Cell Carcinoma. Eur Urol, 87(2), 143–154. https://doi.org/10.1016/j.eururo.2024.10.019
Barragan-Carrillo, Regina, Eddy Saad, Renee-Maria Saliby, Maxine Sun, Laurence Albiges, Axel Bex, Daniel Heng, et al. “First and Second-line Treatments in Metastatic Renal Cell Carcinoma.Eur Urol 87, no. 2 (February 2025): 143–54. https://doi.org/10.1016/j.eururo.2024.10.019.
Barragan-Carrillo R, Saad E, Saliby R-M, Sun M, Albiges L, Bex A, et al. First and Second-line Treatments in Metastatic Renal Cell Carcinoma. Eur Urol. 2025 Feb;87(2):143–54.
Barragan-Carrillo, Regina, et al. “First and Second-line Treatments in Metastatic Renal Cell Carcinoma.Eur Urol, vol. 87, no. 2, Feb. 2025, pp. 143–54. Pubmed, doi:10.1016/j.eururo.2024.10.019.
Barragan-Carrillo R, Saad E, Saliby R-M, Sun M, Albiges L, Bex A, Heng D, Mejean A, Motzer RJ, Plimack ER, Powles T, Rini BI, Zhang T, Choueiri TK. First and Second-line Treatments in Metastatic Renal Cell Carcinoma. Eur Urol. 2025 Feb;87(2):143–154.
Journal cover image

Published In

Eur Urol

DOI

EISSN

1873-7560

Publication Date

February 2025

Volume

87

Issue

2

Start / End Page

143 / 154

Location

Switzerland

Related Subject Headings

  • Urology & Nephrology
  • Protein Kinase Inhibitors
  • Neoplasm Metastasis
  • Kidney Neoplasms
  • Immune Checkpoint Inhibitors
  • Humans
  • Carcinoma, Renal Cell
  • 3202 Clinical sciences
  • 1103 Clinical Sciences