American Journal of Kidney Diseases
Volume 49, Issue 2 , Pages e23-e29, February 2007

Nephrotic Syndrome After Bevacizumab: Case Report and Literature Review

  • Betsy A. George, MD
  • ,
  • Xin J. Zhou, MD
  • ,
  • Robert Toto, MD

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Robert D. Toto, MD, Mary M. Conroy Professor of Kidney Disease, The University of Texas Southwestern Medical Center Dallas, 5323 Harry Hines Blvd, Dallas, TX 75390-8856.

The University of Texas Southwestern Medical Center Dallas, TX.

Received 5 July 2006; accepted 3 November 2006. published online 02 January 2007.

Bevacizumab, or avastin, is a monoclonal hybrid antibody that binds to and neutralizes vascular endothelial growth factor. It has shown promising efficacy in the adjunctive treatment of patients with several cancers. Recent reports indicated that bevacizumab therapy often was associated with the development of proteinuria, but rarely nephrotic syndrome. In this report, we describe a patient who developed new-onset hypertension and nephrotic syndrome in association with bevacizumab treatment for metastatic pancreatic cancer. Renal biopsy showed an immune-complex–mediated focal proliferative glomerulonephritis. Nephrotic syndrome and hypertension resolved after discontinuation of bevacizumab therapy. The mechanism of bevacizumab-induced glomerulonephritis and nephrotic syndrome is unknown and requires additional investigation. Clinicians should be aware of the potential reversible nephrotoxicity of bevacizumab and should monitor blood pressure and urine protein excretion closely during therapy with this agent.

Index words: Bevacizumab, avastin, nephrotic syndrome, proteinuria, vascular endothelial growth factor (VEGF)

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 Originally published online as doi:10.1053/j.ajkd.2006.11.024 on January 3, 2007.

 Support: This work was supported in part by NIH grant no. 2K24DK002818-06 from the National Institutes of Diabetes and Digestive and Kidney Diseases. Potential conflicts of interest: None.

PII: S0272-6386(06)01692-1

doi:10.1053/j.ajkd.2006.11.024

American Journal of Kidney Diseases
Volume 49, Issue 2 , Pages e23-e29, February 2007