Metastatic sarcomatoid renal cell carcinoma treated with vascular endothelial growth factor-targeted therapy

Ali Reza Golshayan1, Saby George, Daniel Y Heng

  • 1Department of Solid Tumor Oncology, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH 44195, USA.

Abstract

Insights

Vascular endothelial growth factor (VEGF)-targeted therapy shows potential in metastatic renal cell carcinoma (mRCC) with sarcomatoid features. Patients with clear-cell histology and less than 20% sarcomatoid elements may experience better outcomes.

Area of Science:

  • Oncology
  • Medical research

Background:

  • Metastatic renal cell carcinoma (mRCC) with sarcomatoid differentiation is an aggressive subtype.
  • Standard chemotherapy and immunotherapy offer limited efficacy for this mRCC variant.
  • The effectiveness of vascular endothelial growth factor (VEGF)-targeted therapy in sarcomatoid mRCC is not well-established.

Purpose of the Study:

  • To evaluate the efficacy of VEGF-targeted therapy in patients with sarcomatoid mRCC.
  • To determine objective response rates, tumor shrinkage, progression-free survival (PFS), and overall survival (OS) in this patient cohort.

Main Methods:

  • Retrospective identification of patients with mRCC and sarcomatoid features treated with VEGF-targeted therapy.
  • Review of pathology slides to quantify the percentage of sarcomatoid differentiation.
  • Analysis of treatment response, including objective response rate, tumor burden shrinkage, PFS, and OS.

Main Results:

  • Forty-three patients with sarcomatoid mRCC were analyzed; median sarcomatoid features were 14%.
  • Partial responses were observed in 19% of patients, primarily those with clear-cell histology and <20% sarcomatoid components.
  • Median PFS was 5.3 months and median OS was 11.8 months, with 53% achieving some tumor shrinkage.

Conclusions:

  • VEGF-targeted therapy can induce objective responses and tumor shrinkage in sarcomatoid mRCC.
  • Clear-cell histology and a lower percentage of sarcomatoid differentiation may predict a better response to VEGF-targeted therapy.

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