Impaired coronary flow reserve in metastatic cancer patients treated with sunitinib

F Sen1, I Yildiz, M Basaran

  • 1Department of Medical Oncology, Institute of Oncology, Istanbul University, Istanbul, Turkey.

Abstract

Insights

Sunitinib treatment for metastatic cancers impairs coronary flow reserve (CFR), a marker of endothelial function. Impaired CFR correlates with treatment duration and inflammation, suggesting a link to sunitinib-induced hypertension.

Area of Science:

  • Cardiovascular Medicine
  • Oncology
  • Pharmacology

Background:

  • Hypertension is a significant side effect of sunitinib, an angiogenesis inhibitor used for metastatic renal cell carcinoma (mRCC) and gastrointestinal stromal tumors (GIST).
  • Endothelial dysfunction is implicated in sunitinib-induced hypertension.
  • Coronary flow reserve (CFR) assessed by trans-thoracic Doppler echocardiography (TTDE) reflects coronary microvascular and endothelial function.

Purpose of the Study:

  • To evaluate endothelial and coronary microvascular function in mRCC and GIST patients undergoing sunitinib treatment using TTDE.
  • To investigate the relationship between sunitinib treatment and CFR.

Main Methods:

  • A cross-sectional study involving 18 cancer patients on sunitinib and 27 healthy controls.
  • Collected patient data included TSH, lipid profile, creatinine, hemoglobin, glucose, CRP, ESR, and anthropometric parameters.
  • CFR was measured using Vivid 7 echocardiography.

Main Results:

  • CFR was significantly lower in sunitinib-treated patients compared to controls (1.82±0.4 vs 2.71±0.8, p < 0.001).
  • Impaired CFR was observed in 72% of patients.
  • CFR showed an inverse correlation with sunitinib treatment duration (r=-0.36, p=0.01), hs-CRP (r=-0.574, p=0.01), and ESR (r=-0.5, p=0.02).

Conclusions:

  • Sunitinib treatment significantly impairs CFR in cancer patients.
  • Impaired CFR is linked to the duration of sunitinib therapy and elevated inflammation markers.
  • CFR may serve as a valuable indicator of endothelial dysfunction in patients receiving sunitinib.

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