TY - JOUR
T1 - Relapse, rebound, and psoriasis adverse events
T2 - An advisory group report
AU - Carey, Wayne
AU - Glazer, Scott
AU - Gottlieb, Alice B.
AU - Lebwohl, Mark
AU - Leonardi, Craig
AU - Menter, Alan
AU - Papp, Kim
AU - Rundle, Amy Chen
AU - Toth, Darryl
N1 - Funding Information:
Drs Carey and Glazer have no conflict of interest to disclose. Dr Gottlieb is an investigator and consultant for Genentech Inc. Dr Lebwohl or members of his faculty have been investigators for Abbott Laboratories, Amgen Inc, Biogen Idec, Centocor Inc, and Genentech Inc; Dr Lebwohl has also been a consultant or speaker for Allergan, Amgen Inc, Biogen Idec, and Genentech Inc. Dr Leonardi has received educational grant support from and has served on the speakers bureau and advisory board for Genentech Inc. Dr Menter has received research support and/or is a consultant and/or lecturer for Abbott Laboratories, Amgen Inc, Biogen Idec, Centocor Inc, Genentech Inc, Serono International SA, and Xoma, LLC. Dr Papp is a consultant, an investigator, and an advisory board member for Genentech Inc, Serono International SA, and Xoma, LLC; he is on the Serono International SA speakers bureau. Ms Rundle is an employee and a stock shareholder of Genentech Inc. Dr Toth is an investigator and member of the advisory board and speakers bureau for Genentech Inc.
PY - 2006/4
Y1 - 2006/4
N2 - Psoriasis is a chronic disease, the severity of which varies among patients and changes unpredictably over time in individual patients. Psoriasis can be exacerbated during treatment by infection, endocrine factors, hypocalcemia, medications, psychologic stress, skin trauma, or other factors. Patients who discontinue treatments may experience a return of disease - relapse - or worsening of disease - rebound. The National Psoriasis Foundation (NPF) proposed standardized definitions of relapse and rebound. Efalizumab, a recombinant humanized immunoglobulin G-1 monoclonal antibody, is approved for the management of psoriasis. During efalizumab clinical trials, a small percentage of patients experienced protocol-defined adverse events related to psoriasis. After publication of the NPF definition of rebound, post hoc exploratory analyses of the efalizumab clinical trial data were performed. The efalizumab clinical trial investigators discussed their observations, the analyses, and their individual approaches to the treatment of patients receiving or discontinuing efalizumab therapy, the conclusions of which are described herein.
AB - Psoriasis is a chronic disease, the severity of which varies among patients and changes unpredictably over time in individual patients. Psoriasis can be exacerbated during treatment by infection, endocrine factors, hypocalcemia, medications, psychologic stress, skin trauma, or other factors. Patients who discontinue treatments may experience a return of disease - relapse - or worsening of disease - rebound. The National Psoriasis Foundation (NPF) proposed standardized definitions of relapse and rebound. Efalizumab, a recombinant humanized immunoglobulin G-1 monoclonal antibody, is approved for the management of psoriasis. During efalizumab clinical trials, a small percentage of patients experienced protocol-defined adverse events related to psoriasis. After publication of the NPF definition of rebound, post hoc exploratory analyses of the efalizumab clinical trial data were performed. The efalizumab clinical trial investigators discussed their observations, the analyses, and their individual approaches to the treatment of patients receiving or discontinuing efalizumab therapy, the conclusions of which are described herein.
UR - https://www.scopus.com/pages/publications/32544441226
U2 - 10.1016/j.jaad.2005.10.029
DO - 10.1016/j.jaad.2005.10.029
M3 - Article
C2 - 16488339
AN - SCOPUS:32544441226
SN - 0190-9622
VL - 54
SP - S171-S181
JO - Journal of the American Academy of Dermatology
JF - Journal of the American Academy of Dermatology
IS - 4 SUPPL.
ER -