Mager Layna, Gardeen Samantha, Carr David R, Shahwan Kathryn T
College of Medicine, The Ohio State University, Columbus, OH, USA.
Division of Dermatology, HealthPartners, Minneapolis, MN, USA.
Clin Cosmet Investig Dermatol. 2023 Aug 9;16:2135-2142. doi: 10.2147/CCID.S381471. eCollection 2023.
Five percent of patients with cutaneous squamous cell carcinoma develop locally advanced or metastatic disease that is not amenable to definitive surgical or radiation therapy. Cemiplimab, an antibody against programmed death receptor-1, was approved in the United States for the treatment of locally advanced and metastatic cutaneous squamous cell carcinoma in 2018. We performed a literature review on the use of cemiplimab in cutaneous squamous cell carcinoma, with an emphasis on efficacy, safety and tolerability, patient selection, and future directions. Embase and PubMed were searched for relevant terms, and 23 peer-reviewed journal articles presenting primary data on cemiplimab treatment in 5 or more subjects with cutaneous squamous cell carcinoma were included and summarized. Objective response rates in locally advanced and metastatic disease ranged from 42.9% to 50.8% in Phase I/II clinical trials and 32-77% (median 58%) in post-approval observational studies. Phase II trials looking at neoadjuvant use also had favorable response rates. Real-world studies demonstrated cemiplimab efficacy in periorbital tumors, tumors with large caliber perineural invasion, and tumors in solid organ transplant recipients. Cemiplimab was safe and well-tolerated in most patients. While side effects such as fatigue, diarrhea, pruritus, and rash were fairly common, only 9.8% of adverse events required cessation of therapy in phase II trials. Severe adverse events were primarily immune-mediated, including pneumonitis, myocarditis, myositis, and autoimmune hepatitis; the risk of treatment-related death was 3% in clinical trials. Further research on cemiplimab therapy in cutaneous squamous cell carcinoma is needed, and trials are now underway to obtain Phase IV long-term real-world data, further data on adjuvant and neoadjuvant use, and additional data in special populations such as stem cell and solid organ transplant recipients.
5%的皮肤鳞状细胞癌患者会发展为局部晚期或转移性疾病,无法接受确定性手术或放射治疗。西米普利单抗是一种抗程序性死亡受体-1抗体,于2018年在美国被批准用于治疗局部晚期和转移性皮肤鳞状细胞癌。我们对西米普利单抗在皮肤鳞状细胞癌中的应用进行了文献综述,重点关注疗效、安全性和耐受性、患者选择及未来方向。在Embase和PubMed中搜索相关术语,纳入并总结了23篇经同行评审的期刊文章,这些文章呈现了西米普利单抗治疗5名或更多皮肤鳞状细胞癌患者的原始数据。在I/II期临床试验中,局部晚期和转移性疾病的客观缓解率为42.9%至50.8%,在批准后观察性研究中为32%-77%(中位值58%)。研究新辅助使用的II期试验也有良好的缓解率。真实世界研究表明西米普利单抗在眶周肿瘤、伴有大口径神经周围浸润的肿瘤以及实体器官移植受者的肿瘤中有效。西米普利单抗在大多数患者中安全且耐受性良好。虽然疲劳、腹泻、瘙痒和皮疹等副作用相当常见,但在II期试验中只有9.8%的不良事件需要停止治疗。严重不良事件主要是免疫介导的,包括肺炎、心肌炎、肌炎和自身免疫性肝炎;临床试验中与治疗相关的死亡风险为3%。需要对西米普利单抗治疗皮肤鳞状细胞癌进行进一步研究,目前正在进行试验以获取IV期长期真实世界数据、辅助和新辅助使用的更多数据以及干细胞和实体器官移植受者等特殊人群的更多数据。