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头颈部癌患者在放疗期间联合使用西妥昔单抗时严重放射性皮炎的高发生率:欧洲癌症研究与治疗组织(EORTC)各机构的一项调查结果

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

作者信息

Giro Christian, Berger Bernhard, Bölke Edwin, Ciernik I Frank, Duprez Frederic, Locati Laura, Maillard Sophie, Ozsahin Mahmut, Pfeffer Raphael, Robertson A Gerry, Langendijk Johannes A, Budach Wilfried

机构信息

Department of Radiation Oncology, University Hospital Düsseldorf, Germany.

出版信息

Radiother Oncol. 2009 Feb;90(2):166-71. doi: 10.1016/j.radonc.2008.09.007. Epub 2008 Oct 30.

DOI:10.1016/j.radonc.2008.09.007
PMID:18977050
Abstract

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.

摘要

目的

在欧洲癌症研究与治疗组织(EORTC)的各中心,对采用放疗(RT)联合西妥昔单抗治疗头颈癌(HNC)期间III级或IV级放射性皮炎的发生率进行研究。

材料与方法

向EORTC放射肿瘤学组和头颈组的所有成员(111个机构)发送了一份调查问卷,以评估西妥昔单抗和放疗在HNC治疗中的广泛应用情况,并估计与该方案相关的放射野中III级和IV级皮肤反应的发生频率。还记录了合并症、放疗方案和联合用药情况。

结果

我们收到了来自11个国家28个机构的回复。共有来自15个机构的125例HNC患者接受了西妥昔单抗联合RT治疗。71例患者有关于皮肤反应的信息。其中36例在放疗野中无III/IV级不良反应,15例为III级,20例为IV级放射性皮炎。未发现III级和IV级放射性皮炎与肝功能不全或肾功能不全等合并症之间存在可检测到的关联。

结论

根据调查问卷结果,在接受西妥昔单抗联合RT治疗的HNC患者中,49%观察到III/IV级放射性皮炎。建议在RT加西妥昔单抗治疗期间对皮肤副作用进行系统的临床监测,以确保该方案的安全性。

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