Life-threatening complications associated with the tyrosine kinase inhibitor sunitinib malate

Urol Int. 2010;85(4):475-8. doi: 10.1159/000321175. Epub 2010 Oct 26.

Abstract

Adverse events associated with sunitinib, such as cardiac toxicities, renal damage, and hemostatic complications, are well known. The authors report 3 cases in which patients experienced severe life-threatening complications after commencing sunitinib treatment. One patient developed heart failure with dilation of the left ventricle and decrease in the ejection fraction after one cycle of sunitinib and required treatment with an angiotensin-converting enzyme inhibitor, loop diuretics, and dobutamine. Another patient developed coronary artery stenosis after one cycle of sunitinib and was managed through percutaneous coronary intervention. Although follow-on coronary angiography revealed normal findings after 6 further cycles of sunitinib, this patient eventually expired due to multi-organ failure. The third patient had chronic renal failure before sunitinib treatment and required hemodialysis due to acute-on-chronic renal failure after commencing sunitinib treatment.

Publication types

  • Case Reports

MeSH terms

  • Acute Kidney Injury / chemically induced*
  • Acute Kidney Injury / diagnosis
  • Acute Kidney Injury / therapy
  • Angioplasty, Balloon, Coronary
  • Antineoplastic Agents / adverse effects*
  • Carcinoma, Renal Cell / drug therapy*
  • Cardiovascular Agents / therapeutic use
  • Coronary Stenosis / chemically induced*
  • Coronary Stenosis / diagnosis
  • Coronary Stenosis / therapy
  • Fatal Outcome
  • Female
  • Heart Failure / chemically induced*
  • Heart Failure / diagnosis
  • Heart Failure / drug therapy
  • Humans
  • Indoles / adverse effects*
  • Kidney Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Multiple Organ Failure / chemically induced
  • Protein Kinase Inhibitors / adverse effects*
  • Pyrroles / adverse effects*
  • Renal Dialysis
  • Sunitinib
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Cardiovascular Agents
  • Indoles
  • Protein Kinase Inhibitors
  • Pyrroles
  • Sunitinib