Activity of Systemic Treatments After Cabozantinib Failure in Advanced Metastatic Renal Cell Carcinoma

Clin Genitourin Cancer. 2022 Feb;20(1):80-87. doi: 10.1016/j.clgc.2021.09.001. Epub 2021 Sep 24.

Abstract

Background: Cabozantinib, a potent multityrosine kinases inhibitor (TKI), has demonstrated overall survival (OS) benefit over everolimus in patients previously treated with VEGFR TKI for metastatic Renal Cell Carcinoma (mRCC). The efficacy of systemic treatments after cabozantinib failure has not been investigated.

Materials and methods: We conducted a retrospective study on patients receiving systemic treatment after cabozantinib failure in heavily pretreated patient with mRCC. We assessed Time to Treatment Failure (TTF), OS and objective response rate (ORR).

Results: Among 150 patients treated with cabozantinib in our institution, 56 (37.3%) received subsequent systemic therapy and were eligible for the analysis. IMDC prognostic group was good, intermediate and poor in 11 (19.6%), 24 (42.9%) and 11 (19.6%) patients, respectively. Cabozantinib was administered mainly as a second (41.1%), or third (33.9%) line treatment. axitinib or immune-checkpoint inhibitors were the subsequent treatment in 18 (34.8%) patients for each everolimus (n:16, 28.6%), other angiogenesis inhibitors (n:4, 7.1%) TTF and OS from subsequent systemic therapy after cabozantinib failure were 2.8 months (95%CI 1.9-3.7) and 7.7 months (95%CI 4.4-10.8), respectively. ORR was 8.7% and 2 patients with axitinib and 2 patients treated with Immune checkpoint inhibitors achieved a partial response.

Conclusion: Overall, activity of systemic therapies after cabozantinib was limited.

Keywords: Axitinib; Cabozantinib; Everolimus; Immune-checkpoint inhibitors; Metastatic renal cell carcinoma.

MeSH terms

  • Anilides
  • Antineoplastic Agents*
  • Axitinib / therapeutic use
  • Carcinoma, Renal Cell* / pathology
  • Everolimus / therapeutic use
  • Female
  • Humans
  • Immune Checkpoint Inhibitors
  • Kidney Neoplasms* / pathology
  • Male
  • Protein Kinase Inhibitors
  • Pyridines
  • Retrospective Studies

Substances

  • Anilides
  • Antineoplastic Agents
  • Immune Checkpoint Inhibitors
  • Protein Kinase Inhibitors
  • Pyridines
  • cabozantinib
  • Everolimus
  • Axitinib