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达可替尼诱导的甲沟炎与一名非小细胞肺癌患者的PRIDE综合征相关。

Dacomitinib-Induced Paronychia Associated With PRIDE Syndrome in a Patient With Non-Small Cell Lung Cancer.

作者信息

Sahadevan Geethanjali, Cm Divyashanthi, Sivamani Kalaimani

机构信息

Dermatology, Jawaharlal Institute of Postgraduate Medical Education & Research, Karaikal, IND.

Pharmacology, Jawaharlal Institute of Postgraduate Medical Education & Research, Puducherry, IND.

出版信息

Cureus. 2025 Jun 11;17(6):e85774. doi: 10.7759/cureus.85774. eCollection 2025 Jun.

Abstract

Epidermal growth factor receptor (EGFR) inhibitors are essential for treating non-small cell lung cancer (NSCLC) with EGFR mutations, but they frequently cause cutaneous toxicities collectively referred to as papulopustules and/or paronychia, regulatory abnormalities of hair growth, itching, and dryness due to epidermal growth factor receptor inhibitors (PRIDE) syndrome. This case describes a 55-year-old male with advanced NSCLC who developed toe-predominant paronychia, a papulopustular rash localized to the trunk and limbs, and diarrhea four to eight weeks after initiating first-line therapy with dacomitinib. Notably, causality was evaluated using multiple validated tools - Naranjo, WHO-UMC, and Liverpool Causality Assessment Tool - all of which indicated a "probable" relationship. Importantly, these adverse effects were managed symptomatically without the need for discontinuation or dose reduction of dacomitinib. This case contributes to the literature by documenting an atypical anatomical distribution (toe-predominant), early onset, and successful continuation of therapy, highlighting the importance of early recognition, pharmacologic assessment, and adverse event reporting to optimize the safety of EGFR inhibitors in clinical practice.

摘要

表皮生长因子受体(EGFR)抑制剂对于治疗具有EGFR突变的非小细胞肺癌(NSCLC)至关重要,但它们经常引起统称为丘疹脓疱和/或甲沟炎、由于表皮生长因子受体抑制剂导致的毛发增长调节异常、瘙痒和干燥的皮肤毒性(PRIDE综合征)。本病例描述了一名55岁的晚期NSCLC男性患者,在开始使用达可替尼进行一线治疗后的4至8周出现了以脚趾为主的甲沟炎、局限于躯干和四肢的丘疹脓疱性皮疹以及腹泻。值得注意的是,使用多种经过验证的工具——纳伦霍、世界卫生组织药物不良反应协作中心(WHO-UMC)和利物浦因果关系评估工具——对因果关系进行了评估,所有这些工具均表明存在“可能”的关系。重要的是,这些不良反应通过对症处理得到了控制,无需停用或减少达可替尼的剂量。本病例通过记录非典型的解剖分布(以脚趾为主)、早期发病以及治疗的成功持续,为文献做出了贡献,强调了早期识别、药物评估和不良事件报告对于优化临床实践中EGFR抑制剂安全性的重要性。

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