Park Soo J, Ellison David M, Weight Ryan, Homsi Jade, Rabinowits Guilherme, Ruiz Emily S, Strasswimmer John, Simmons Josh, Panella Timothy, Quek Ruben Gw, Pouliot Jean-Francois, Khushalani Nikhil I
Department of Medicine, Division of Hematology and Oncology, University of California San Diego, La Jolla, CA, USA.
Charleston Oncology, Charleston, SC, USA.
Future Oncol. 2025 Feb;21(4):431-436. doi: 10.1080/14796694.2024.2448416. Epub 2025 Jan 11.
Patients diagnosed with metastatic basal cell carcinoma (BCC) have a poor prognosis. The current standard of care for adults with locally advanced or metastatic BCC who are not candidates for surgery or radiation therapy is treatment with hedgehog pathway inhibitors (HHIs). For patients who progress while on this therapy, further treatment options are limited. There is also a need for real-world clinical practice data on the clinical characteristics, management, disease progression, and survivorship of these patients. The ongoing CemiplimAb-rwlc Survivorship and Epidemiology (CASE) study is a phase IV, multicenter, prospective, noninterventional survivorship and epidemiology cohort study evaluating the effectiveness and safety of cemiplimab, a fully human immunoglobulin G4 monoclonal antibody that blocks the interaction between the programmed cell death-1 (PD-1) receptor and its ligands. This paper describes one cohort of the CASE study of patients with locally advanced or metastatic BCC who have failed or are intolerant of HHIs or for whom HHI therapy is not appropriate. Outcome measures of the study include response to treatment, quality of life, safety, treatment patterns, patient experience, and survival. This study could provide a more complete characterization of this patient population and fill knowledge gaps related to real-world treatment utilization and patient outcomes.Clinical Trial registration: NCT03836105.
被诊断为转移性基底细胞癌(BCC)的患者预后较差。对于不适合手术或放疗的局部晚期或转移性BCC成年患者,目前的标准治疗方法是使用刺猬通路抑制剂(HHIs)进行治疗。对于在这种治疗过程中病情进展的患者,进一步的治疗选择有限。此外,还需要关于这些患者的临床特征、管理、疾病进展和生存情况的真实世界临床实践数据。正在进行的西米普利单抗-rwlc生存与流行病学(CASE)研究是一项IV期、多中心、前瞻性、非干预性生存与流行病学队列研究,旨在评估西米普利单抗的有效性和安全性。西米普利单抗是一种完全人源化的免疫球蛋白G4单克隆抗体,可阻断程序性细胞死亡蛋白1(PD-1)受体与其配体之间的相互作用。本文描述了CASE研究中的一组局部晚期或转移性BCC患者,这些患者对HHIs治疗无效或不耐受,或HHIs治疗不适用。该研究的结果指标包括治疗反应、生活质量、安全性、治疗模式、患者体验和生存率。这项研究可以更全面地描述这一患者群体,并填补与真实世界治疗利用和患者结局相关的知识空白。临床试验注册号:NCT03836105。