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Management of dermatologic toxicities related to epidermal growth factor receptor inhibitor therapy across Europe: can we get a consensus?

机译:在欧洲管理与表皮生长因子受体抑制剂治疗有关的皮肤毒性:我们能否达成共识?

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摘要

To date, there are no phase III trial data that can guide healthcare professionals in managing toxicities of epidermal growth factor receptor inhibitors (EGFRIs). This exploratory survey assessed the similarities and differences in nursing management of EGFRI-related toxicities across 10 European countries. A questionnaire that was sent to ten nurses who specialize in the treatment of patients with EGFRI asked about the prevention and treatment of acneiform rash, dry skin/eczema, fissures, paronychia, and pyogenic granuloma. Responses from seven nurses showed that overall (with the exception of rash), treatment differed markedly between countries in the management of dermatologic toxicities. These substantial differences across the European hospitals surveyed suggest that it might be worthwhile to develop treatment algorithms by conducting a consensus conference or a follow-up survey with several assessments and a larger sample.
机译:迄今为止,尚无可指导医疗保健专业人员管理表皮生长因子受体抑制剂(EGFRI)毒性的III期试验数据。这项探索性调查评估了欧洲10个国家在EGFRI相关毒性的护理管理方面的异同。向十位专门治疗EGFRI患者的护士发送了一份调查问卷,询问预防和治疗痤疮样皮疹,皮肤干燥/湿疹,裂痕,甲沟炎和化脓性肉芽肿。七名护士的回应表明,总体上(皮疹除外),各国之间在皮肤毒性的管理上存在显着差异。在接受调查的欧洲各医院中,这些实质性差异表明,可能有必要通过召开共识会议或后续调查(包括多个评估和更大样本)来开发治疗算法。

著录项

  • 期刊名称 ecancermedicalscience
  • 作者

    L Lemmens;

  • 作者单位
  • 年(卷),期 2011(5),-1
  • 年度 2011
  • 页码 220
  • 总页数 10
  • 原文格式 PDF
  • 正文语种
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