Sunitinib in Metastatic Renal Cell Carcinoma: Recommendations for Management of Noncardiovascular Toxicities

  • Christian Kollmannsberger
    a British Columbia Cancer Agency Vancouver Cancer Centre, Vancouver, British Columbis, Canada;
  • Georg Bjarnason
    b Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada;
  • Patrick Burnett
    c Vanderbilt University Medical Center, Nashville, Tennessee, USA;
  • Patricia Creel
    d Duke University Medical Center, Durham, North Carolina, USA;
  • Mellar Davis
    e Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, USA;
  • Nancy Dawson
    f Lombardi Comprehensive Cancer Center, Georgetown University, Washington, D.C., USA;
  • Darren Feldman
    g Memorial Sloan-Kettering Cancer Center, New York, New York, USA;
  • Suzanne George
    h Dana Farber Cancer Institute, Boston, Massachusetts, USA;
  • Jerome Hershman
    i David Geffen School of Medicine, Los Angeles, California, USA;
  • Thomas Lechner
    j Pfizer Oncology, New York, New York, USA;
  • Amy Potter
    h Dana Farber Cancer Institute, Boston, Massachusetts, USA;
  • Eric Raymond
    k Service Inter-Hospitalier de Cancérologie Beaujon-Bichat, Clichy, France;
  • Nathaniel Treister
    l Brigham and Women's Hospital, Boston, Massachusetts, USA;
  • Laura Wood
    e Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, USA;
  • Shenhong Wu
    m Stony Brook University Medical Center, Stony Brook, New York, USA
  • Ronald Bukowski
    e Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, USA;

説明

<jats:title>Abstract</jats:title> <jats:p>The multitargeted tyrosine-kinase inhibitor sunitinib has emerged as one of the standards of care for good- and intermediate-risk metastatic renal cell carcinoma. Although generally associated with acceptable toxicity, sunitinib exhibits a novel and distinct toxicity profile that requires monitoring and management. Fatigue, diarrhea, anorexia, oral changes, hand-foot syndrome and other skin toxicity, thyroid dysfunction, myelotoxicity, and hypertension seem to be the most common and clinically relevant toxicities of sunitinib. Drug dosing and treatment duration are correlated with response to treatment and survival. Treatment recommendations for hypertension have been published but, currently, no standard guidelines exist for the management of noncardiovascular side effects. To discuss the optimal management of noncardiovascular side effects, an international, interdisciplinary panel of experts gathered in November 2009. Existing literature on incidence, severity, and underlying mechanisms of side effects as well as on potential treatment options were carefully reviewed and discussed. On the basis of these proceedings and the thorough review of the existing literature, recommendations were made for the monitoring, prevention, and treatment of the most common noncardiovascular side effects and are summarized in this review. The proactive assessment and consistent and timely management of sunitinib-related side effects are critical to ensure optimal treatment benefit by allowing appropriate drug dosing and prolonged treatment periods.</jats:p>

収録刊行物

  • The Oncologist

    The Oncologist 16 (5), 543-553, 2011-04-13

    Oxford University Press (OUP)

被引用文献 (2)*注記

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