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Strategies for optimizing treatment with efalizumab in moderate to severe psoriasis
Authors:Kim A. Papp  Vincent Ho  Richard Langley  Charles Lynde  Yves Poulin  Neil Shear  John Toole  Catherine Zip
Affiliation:1.Probity Medical Research,Waterloo;2.University of British Columbia,Vancouver;3.Dalhousie University Queen Elizabeth II Health Science Centre,Halifax;4.University of Toronto, University Health Network, and Lynde Centre for Dermatology,Markham;5.Laval University and Centre Dermatologique,Sainte Foy;6.Sunnybrook & Women’s College, University of Toronto Medical School and Ventana Clinical Research Corp.,Toronto;7.University of Manitoba, Dermadvances Research Winnipeg,Winnipeg;8.University of Calgary and The Dermatology Centre,Calgary
Abstract:With the advent of biological therapies for the treatment of plaque psoriasis, guidance on the usage of these new agents has become necessary. One such agent, efalizumab, a humanized recombinant monoclonal IgG1 antibody developed to target T-cell-mediated inflammation, provides rapid and sustained efficacy for many psoriasis patients. This article explores the pretreatment, initiation, and treatment phases with efalizumab therapy. In the pretreatment phase, physicians need to assess patients’ disease state and educate them about the course of efalizumab treatment. Prior to initiation, physicians need to establish stable disease, ensure an adequate transition or washout of any prior psoriasis therapeutics, and obtain baseline platelet counts. After initiating treatment, both physician and patient must participate in disease monitoring. Patients responding favourably may receive continuous treatment. Those who do not respond to the drug or who experience adverse events should be managed appropriately in order to continue therapy or be transitioned onto another agent. A growing body of clinical evidence, as well as experience from clinical investigators, has provided much insight into the management strategies for patients undergoing treatment with efalizumab.
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