Risk factors for and pre-medications to prevent cetuximab-induced infusion reactions in patients with squamous cell carcinoma of the head and neck

被引:18
作者
Touma, Waseem [1 ]
Koro, Sami S. [2 ]
Ley, Jessica [2 ]
Wildes, Tanya M. [2 ,3 ]
Michel, Loren [2 ,3 ]
Tao, Yu [4 ]
Adkins, Douglas [2 ,3 ]
机构
[1] Dept Internal Med, Div Hosp Med, St Louis, MO USA
[2] Dept Internal Med, Div Med Oncol, St Louis, MO USA
[3] Alvin J Siteman Canc Ctr, St Louis, MO USA
[4] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
关键词
Cetuximab; Infusion reaction; Risk factors; Pre-medication; METASTATIC COLORECTAL-CANCER; PLUS IRINOTECAN; NORTH-CAROLINA; PHASE-II;
D O I
10.1016/j.oraloncology.2014.06.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Cetuximab, a chimeric monoclonal antibody, is the only targeted therapy approved for squamous cell carcinoma of the head and neck (SCCHN). Infusion reactions (IRs) occur in 6-18% of patients pre-medicated with diphenhydramine. Evidence for clinical risk factors for IRs is limited and the benefit of additional pre-medication to prevent IRs is unclear. Materials and methods: A retrospective, single institution study of 243 SCCHN patients treated with cetuximab to evaluate potential risk factors for IRs and to assess the efficacy of additional pre-medications (nebulized albuterol and intravenous (IV) corticosteroids and/or H-2-blockers) to decrease the risk of IR. Results: IR (grades 1-4) and high grade (grades 3-4 only) IR occurred in 47 (19.3%) and 16 (6.6%) patients, respectively. Multivariate analysis identified Caucasian race (OR7.11, p = 0.003), medication allergy (OR3.74, p = 0.002), and blood eosinophils >3% (OR2.75, p = 0.01) independently increased the risk of IR; Caucasian race (OR5.57, p = 0.007) and medication allergy (OR4.10, p = 0.0007) increased the risk of high grade IR. IR (grades 1-4) and high grade IR occurred in 31.8% and 22.7% pre-medicated with diphenhydramine alone. Univariate analysis identified albuterol, famotidine, and corticosteroids decreased the risk of high grade IR. Furthermore, there was a significant difference between the possible combinations of the pre-medications and the risk of high grade IR by Fisher Exact test (p = 0.003) whereby the combination of albuterol, famotidine and corticosteroids was effective in preventing high grade IR. Thirty (64%) of the 47 patients who developed an IR were re-challenged and did not experience a recurrence of an IR. Conclusion: These data may be used to identify patients at higher risk for cetuximab-induced IR who may be advised to not receive cetuximab or who may benefit from additional pre-medications to decrease the risk of a high grade IR. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:895 / 900
页数:6
相关论文
共 24 条
[21]   Reduced Incidence of Infusion-Related Reactions in Metastatic Colorectal Cancer During Treatment With Cetuximab Plus Irinotecan With Combined Corticosteroid and Antihistamine Premedication [J].
Siena, Salvatore ;
Glynne-Jones, Robert ;
Adenis, Antoine ;
Thaler, Josef ;
Preusser, Peter ;
Aranda Aguilar, Enrique ;
Aapro, Matti S. ;
Loos, Anja H. ;
Esser, Regina ;
Wilke, Hansjochen .
CANCER, 2010, 116 (07) :1827-1837
[22]   Platinum-based chemotherapy plus cetuximab in head and neck cancer [J].
Vermorken, Jan B. ;
Mesia, Ricard ;
Rivera, Fernando ;
Remenar, Eva ;
Kawecki, Andrzej ;
Rottey, Sylvie ;
Erfan, Jozsef ;
Zabolotnyy, Dmytro ;
Kienzer, Heinz-Roland ;
Cupissol, Didier ;
Peyrade, Frederic ;
Benasso, Marco ;
Vynnychenko, Ihor ;
De Raucourt, Dominique ;
Bokemeyer, Carsten ;
Schueler, Armin ;
Amellal, Nadia ;
Hitt, Ricardo .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (11) :1116-1127
[23]  
Vermorken JB, 2007, J CLIN ONCOL, V25, P2171, DOI 10.1200/JCO.2006.06.7447
[24]   Cetuximab Plus Irinotecan in Heavily Pretreated Metastatic Colorectal Cancer Progressing on Irinotecan: MABEL Study [J].
Wilke, Hansjochen ;
Glynne-Jones, Robert ;
Thaler, Josef ;
Adenis, Antoine ;
Preusser, Peter ;
Aguilar, Enrique Aranda ;
Aapro, Matti S. ;
Esser, Regina ;
Loos, Anja H. ;
Siena, Salvatore .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (33) :5335-5343