High rate of severe radiation dermatitis during radiation therapy with concurrent cetuximab in head and neck cancer: Results of a survey in EORTC institutes

被引:129
作者
Giro, Christian [1 ]
Berger, Bernhard [2 ]
Boelke, Edwin [1 ]
Ciernik, I. Frank
Duprez, Frederic [3 ]
Locati, Laura [4 ]
Maillard, Sophie [5 ]
Ozsahin, Mahmut [6 ]
Pfeffer, Raphael
Robertson, A. Gerry [7 ]
Langendijk, Johannes A. [8 ]
Budach, Wilfried [1 ]
机构
[1] Univ Hosp Dusseldorf, Dept Radiat Oncol, D-40225 Dusseldorf, Germany
[2] Univ Tubingen Hosp, Dept Radiat Oncol, Tubingen, Germany
[3] Ghent Univ Hosp, Dept Radiat Oncol, Ghent, Belgium
[4] Fdn IRCCS, Ist Nazl Tumori, Dept Med Oncol, Head & Neck Unit, Milan, Italy
[5] Inst Jean Godinot Reims, Dept Radiat Oncol, Reims, France
[6] Univ Lausanne Hosp, Dept Radiat Oncol, Lausanne, Switzerland
[7] Univ Hosp N Glasgow, Dept Radiat Oncol, Glasgow, Lanark, Scotland
[8] Univ Groningen, Univ Med Ctr Groningen, Dept Radiat Oncol, Groningen, Netherlands
关键词
Cetuximab; Radiotherapy; Erythema; Sequelae; Skin reaction; EGFR inhibitors; Radiation dermatitis; Head and neck cancer; SQUAMOUS-CELL CARCINOMA; RADIOTHERAPY PLUS CETUXIMAB; SEVERE CUTANEOUS REACTION; EGFR INHIBITORS; TRIAL; RECEPTOR; ACTIVATION; CHART;
D O I
10.1016/j.radonc.2008.09.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Examination of the rate of grade III or grade IV radiation dermatitis during treatment of head and neck cancer (HNC) with radiotherapy (RT) and concurrent cetuximab in EORTC centres. Materials and method: A questionnaire was sent to all members of the EORTC Radiation Oncology Group and Head and Neck Group (111 institutions) to evaluate the widespread use of cetuximab and radiotherapy in HNC and to estimate the frequency of grades III and IV skin reactions in the radiation portals associated with this protocol. Co-morbidities, RT schedules and co-medications were also recorded. Results: We received responses from 28 institutions in 11 countries. A total of 125 HNC patients from 15 institutions were treated with cetuximab and concurrent RT. Information about the skin reactions was available from 71 patients. Of these 36 had no grade III/IV adverse effects in the RT field, 15 had a grade III and 20 had grade IV radiation dermatitis. No detectable relation of grades III and IV radiation dermatitis with co-morbidities Such as liver insufficiency or renal dysfunction was found. Conclusion: According to the results of the questionnaire, grade III/IV radiation dermatitis is observed in 49% of HNC patients treated with cetuximab and concurrent RT. A systematic clinical monitoring of cutaneous side effects during RT Plus cetuximab is advised to ensure the safety of this protocol. (C) 2008 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 90 (2009) 166-171
引用
收藏
页码:166 / 171
页数:6
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