Impact and management of skin toxicity associated with anti-epidermal growth factor receptor therapy: Survey results

被引:143
作者
Boone, Susan L. [1 ]
Rademaker, Alfred [2 ,3 ]
Liu, Dachao [2 ]
Pfeiffer, Carmen [4 ]
Mauro, David J. [4 ]
Lacouture, Mario E. [1 ,3 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Dermatol, SERIES Clin, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL 60611 USA
[3] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[4] Bristol Myers Squibb Co, Plainsboro, NJ USA
关键词
epidermal growth factor receptor inhibitors; cetuximab; skin toxicity; papulopustular rash; cutaneous side effects;
D O I
10.1159/000112795
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biologic agents targeting the epidermal growth factor receptor (EGFR) have emerged as a robust treatment option for various solid tumors. Despite lower systemic side effects than conventional chemotherapy, the majority of patients treated with these agents experience cutaneous toxicities, including papulopustular rashes, hair and nail changes, xerosis and pruritus, which have a significant impact on health and quality of life. Currently no consensus or management guidelines exist for these untoward events. Therefore, a retrospective survey was carried out across 110 oncology practioners in the US that were administering EGFR inhibitors. Providers were queried on the impact and management of these untoward events in their practices. Responses suggest that combination therapies (topical and oral) were more effective than either therapy alone, and also lead to a more rapid resolution of the papulopustular rash. Providers also reported that patients frequently complained of physical symptoms associated with the rash (itching and pain), and that they had a positive perception when being treated for their cutaneous side effects. The survey results support that attentive cutaneous care is important in patients treated with EGFR inhibitors, and that proactive/combined interventions may enhance quality of life and optimize consistent drug administration. Copyright (C) 2007 S. Karger AG, Basel.
引用
收藏
页码:152 / 159
页数:8
相关论文
共 33 条
[1]   Dermatologic side effects associated with the epidermal growth factor receptor inhibitors [J].
Agero, Anna Liza C. ;
Dusza, Stephen W. ;
Benvenuto-Andrade, Cristiane ;
Busam, Klaus J. ;
Myskowski, Patricia ;
Halpern, Allan C. .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2006, 55 (04) :657-670
[2]  
[Anonymous], 2003, P AM SOC CLIN ONCOL
[3]  
Barankin B, 2002, CAN FAM PHYSICIAN, V48, P712
[4]   Phase I safety, pharmacokinetic, and pharmacodynamic trial of ZD1839, a selective oral epidermal growth factor receptor tyrosine kinase inhibitor, in patients with five selected solid tumor types [J].
Baselga, J ;
Rischin, D ;
Ranson, M ;
Calvert, H ;
Raymond, E ;
Kieback, DG ;
Kaye, SB ;
Gianni, L ;
Harris, A ;
Bjork, T ;
Averbuch, SD ;
Feyereislova, A ;
Swaisland, H ;
Rojo, F ;
Albanell, J .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (21) :4292-4302
[5]  
BREWER CJ, 2005, J CLIN ONCOL S, V23
[6]   Cutaneous side-effects in cancer patients treated with the antiepidermal growth factor receptor antibody C225 [J].
Busam, KJ ;
Capodieci, P ;
Motzer, R ;
Kiehn, T ;
Phelan, D ;
Halpern, AC .
BRITISH JOURNAL OF DERMATOLOGY, 2001, 144 (06) :1169-1176
[7]   Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer [J].
Cunningham, D ;
Humblet, Y ;
Siena, S ;
Khayat, D ;
Bleiberg, H ;
Santoro, A ;
Bets, D ;
Mueser, M ;
Harstrick, A ;
Verslype, C ;
Chau, I ;
Van Cutsem, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) :337-345
[8]   Epidermal growth factor receptor inhibition induces trichomegaly [J].
Dueland, S ;
Sauer, T ;
Lund-Johansen, F ;
Ostenstad, B ;
Tveit, KM .
ACTA ONCOLOGICA, 2003, 42 (04) :345-346
[9]  
*GEN INC, 2007, TARC ERL TABL PACK I
[10]  
*GEN INC, 2007, TARC ERL TABL