在非小细胞肺癌患者中,与纳武单抗诱导的持续疾病反应相关的异常皮肤毒性

G. Galli, C. Proto, M. Cossa, B. Valeri, S. Sdao, D. Signorelli, M. Imbimbo, F. de Braud, M. Garassino, G. Lo Russo
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引用次数: 6

摘要

免疫疗法在治疗各种恶性肿瘤中已显示出疗效。Nivolumab是一种针对程序性死亡-1的免疫检查点抑制剂,已被批准用于非小细胞肺癌(NSCLC)的预处理患者。尽管免疫治疗通常耐受性良好,但免疫治疗可能会因各种免疫介导的不良事件而复杂化。我们描述了一个罕见的皮肤毒性引起的脱发由纳武单抗诱导的非小细胞肺癌患者。病例描述:一名58岁的男性在进展到3线化疗后接受了转移性NSCLC的纳武单抗治疗。该疗法于2016年6月开处方,并引起了快速而显著的疾病反应。在2017年5月出现头发和睫毛部分脱发之前,尼武单抗的耐受性良好。在接下来的几个月里,脱发变得完全并扩展到整个体表。皮肤病学图片与斑秃相符。尝试了局部类固醇治疗,但没有效果。患者拒绝接受全身治疗,目前仍在接受纳武单抗治疗,无新的毒性,且疾病反应持续。结论:本病例提示斑秃可能是免疫检查点药物罕见的免疫相关不良事件。在我们的患者中,它的晚发是罕见的和意想不到的,强调了尼伏单抗引起的毒性的风险并不局限于治疗的开始。尽管斑秃很罕见,但从长期来看,它仍应被认为是免疫检查点抑制剂可能引起的不良事件之一。非小细胞肺癌免疫治疗的毒性和疗效之间的潜在关联值得进一步研究。
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Unusual skin toxicity associated with sustained disease response induced by nivolumab in a patient with non-small cell lung cancer
Introduction: Immunotherapy has shown efficacy in the treatment of different malignancies. Nivolumab, an immune checkpoint inhibitor directed against programmed death-1, has been approved for non-small cell lung cancer (NSCLC) in pretreated patients. Although it is generally well-tolerated, immunotherapy may be complicated by a wide range of immune-mediated adverse events. We describe the case of an uncommon skin toxicity arising as alopecia universalis induced by nivolumab in a patient with NSCLC. Case description: A 58-year-old man received nivolumab for metastatic NSCLC after progression to 3 lines of chemotherapy. The treatment was prescribed in June 2016, and induced a rapid and significant disease response. Nivolumab was well-tolerated until May 2017, when partial alopecia at hair and eyelashes appeared. In the next months, alopecia became complete and extended to the whole body surface. The dermatologic picture was compatible with alopecia areata. A topical steroid therapy was attempted, without benefit. The patient refused systemic treatments and is still undergoing nivolumab without new toxicities and with persistent disease response. Conclusions: This case suggests that alopecia areata may be a rare immune-related adverse event of immune checkpoint agents. Its late onset in our patient is uncommon and unexpected, underlining that the risk of nivolumab-induced toxicity is not limited to the beginning of treatment. Despite its rarity, alopecia areata should be considered in the range of adverse events potentially induced by immune checkpoint inhibitors even in the long term. Potential association between toxicity and efficacy of immunotherapy in NSCLC warrants further investigation.
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