Koch Hein Erica C, Vilbert Maysa, Hirsch Ian, Fernando Ribeiro Mauricio, Muniz Thiago P, Fournier Cynthia, Abdulalem Khaled, Saldanha Erick F, Martinez Erika, Spreafico Anna, Hogg David H, Butler Marcus O, Saibil Samuel D
Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2M9, Canada.
Department of Medicine, Division of Medical Oncology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Cancers (Basel). 2023 Aug 29;15(17):4312. doi: 10.3390/cancers15174312.
Immune checkpoint inhibitors (ICI) cemiplimab and pembrolizumab have revolutionized the treatment of advanced cutaneous squamous cell carcinoma (cSCC). We aimed to evaluate the effectiveness and safety of ICI in a real-world cSCC population, including patients with conditions that would exclude clinical trial participation. In this single-center, retrospective cohort study, we included all non-trial patients with advanced cSCC treated with ICI between 2017 and 2022. We evaluated investigator-assessed best overall response (BOR) and immune-related adverse events (irAEs). We correlated survival outcomes with age, performance status, immune status and irAEs. Of the 36 patients identified, the best overall response (BOR) to ICI was a partial response (PR) in 41.7%, a complete response (CR) in 27.8%, and stable disease in (SD) 13.9%. The progression-free survival (PFS) rate for 1 year was 58.1%; the median PFS was 21.3 months (95% CI 6.4-NE). The 1-year overall survival (OS) was 76.7%, and the median OS was 38.6 months (95% CI 25.4-NE). Immune-compromised patients, ECOG performance 2-3, and age ≥ 75 years were not significantly associated with PFS or OS. IrAE grades 3-4 were seen in 13.9% of patients. In our Canadian experience with real-world patients, ICI was an effective and safe treatment for advanced cSCC patients. Patients achieved great benefits with ICI regardless of age, immune status or ECOG performance status. We acknowledge the small sample size and retrospective methodology as the main limitations of our study.
免疫检查点抑制剂(ICI)西米普利单抗和帕博利珠单抗彻底改变了晚期皮肤鳞状细胞癌(cSCC)的治疗方式。我们旨在评估ICI在真实世界cSCC患者群体中的有效性和安全性,包括那些因病情而被排除在临床试验之外的患者。在这项单中心回顾性队列研究中,我们纳入了2017年至2022年间所有接受ICI治疗的晚期cSCC非试验患者。我们评估了研究者评估的最佳总体缓解(BOR)和免疫相关不良事件(irAE)。我们将生存结果与年龄、体能状态、免疫状态和irAE进行了关联分析。在确定的36例患者中,ICI的最佳总体缓解(BOR)为部分缓解(PR)的占41.7%,完全缓解(CR)的占27.8%,疾病稳定(SD)的占13.9%。1年无进展生存期(PFS)率为58.1%;中位PFS为21.3个月(95%CI 6.4-未达到)。1年总生存期(OS)为76.7%,中位OS为38.6个月(95%CI 25.4-未达到)。免疫功能低下的患者、东部肿瘤协作组(ECOG)体能状态为2-3级以及年龄≥75岁的患者与PFS或OS无显著相关性。13.9%的患者出现了3-4级irAE。根据我们在加拿大对真实世界患者的经验,ICI对晚期cSCC患者是一种有效且安全的治疗方法。无论年龄、免疫状态或ECOG体能状态如何,患者使用ICI都获得了很大益处。我们承认样本量小和回顾性研究方法是我们研究的主要局限性。