Khaddour Karam, Gorell Emily S, Dehdashti Farrokh, Tang Jean Y, Ansstas George
Washington University in Saint Louis, Division of Medical Oncology, Saint Louis, Missouri, USA.
Stanford University School of Medicine, Department of Dermatology, Stanford, California, USA.
Case Rep Oncol. 2020 Jul 30;13(2):911-915. doi: 10.1159/000508933. eCollection 2020 May-Aug.
Recessive dystrophic epidermolysis bullosa (RDEB) is a genodermatosis that leads to skin fragility and chronic wound formation. Patients with RDEB are at risk for cutaneous squamous cell carcinoma (SCC) which is a major cause of morbidity and mortality in these patients. No standard of care exists for the treatment of SCC in this patient population and therapy is based on anecdotal reports and expert opinion. We report a 32-year-old man with RDEB with previously localized SCC who later developed metastatic SCC. He was started on cemiplimab (an immune checkpoint inhibitor) 350 mg IV every 3 weeks. An objective radiological response was noted within 3 cycles. On 14 months follow-up, there was a durable response to treatment clinically and on imaging, without immune-related adverse events. To our knowledge, this is the first case report describing safe administration of immune checkpoint inhibitors in a patient with RDEB with objective and durable response of metastatic SCC. Larger case series and controlled clinical trials are needed to further investigate these medications in the RDEB population, given their high burden of aggressive and often lethal SCC.
隐性营养不良型大疱性表皮松解症(RDEB)是一种遗传性皮肤病,可导致皮肤脆弱和慢性伤口形成。RDEB患者有患皮肤鳞状细胞癌(SCC)的风险,这是这些患者发病和死亡的主要原因。对于该患者群体中SCC的治疗,目前尚无标准治疗方案,治疗基于轶事报道和专家意见。我们报告了一名32岁的RDEB男性患者,其之前患有局限性SCC,后来发展为转移性SCC。他开始接受西米普利单抗(一种免疫检查点抑制剂)治疗,静脉注射350mg,每3周一次。在3个周期内观察到客观的放射学反应。在14个月的随访中,临床和影像学检查均显示对治疗有持久反应,且无免疫相关不良事件。据我们所知,这是第一例描述在患有转移性SCC的RDEB患者中安全使用免疫检查点抑制剂并获得客观持久反应的病例报告。鉴于侵袭性且往往致命的SCC给RDEB人群带来的沉重负担,需要更大规模的病例系列研究和对照临床试验来进一步研究这些药物在RDEB人群中的应用。