Real-World Treatment Patterns and Outcomes of Cemiplimab in Patients with Advanced Cutaneous Squamous Cell Carcinoma Treated in US Oncology Practices

被引:0
|
作者
Ge, Wenzhen [1 ]
Wu, Ning [1 ]
Chen, Chieh-, I [1 ]
Inocencio, Timothy J. [1 ]
Lafontaine, Patrick R. [2 ]
Seebach, Frank [3 ]
Fury, Matthew [4 ]
Harnett, James [1 ]
Ruiz, Emily S. [5 ]
机构
[1] Regeneron Pharmaceut Inc, Dept Hlth Econ & Outcomes Res, Tarrytown, NY USA
[2] Sanofi, Dept Global Hlth Econ & Outcomes Res, Cambridge, MA USA
[3] Regeneron Pharmaceut Inc, Dept Regulatory Affairs, Tarrytown, NY USA
[4] Regeneron Pharmaceut Inc, Dept Clin Sci, Oncol, Tarrytown, NY USA
[5] Dana Farber Canc Inst, Dept Dermatol, Boston, MA USA
来源
关键词
cutaneous squamous cell carcinoma; cemiplimab; immune checkpoint inhibitor; real -world study; skin cancer; PHASE-II; SKIN-CANCER;
D O I
10.2147/CMAR.S445910
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Prior to the Food and Drug Administration approval of cemiplimab in 2018, the median overall survival (OS) for adult patients with advanced CSCC receiving systemic therapy was approximately 8 to 15 months. Limited real-world data are available on cemiplimab for this indication in the US. Patients and Methods: This retrospective cohort study included US patients with advanced CSCC initiating cemiplimab monotherapy in a real-world database (2018-2021). A clinical trial-like sub-cohort was identified using select criteria. Time to treatment discontinuation (TTD), time to next treatment (TTNT), and OS were estimated using Kaplan-Meier methods. Cox proportional hazard models were used to examine prognostic factors associated with OS in the main cohort. Results: The main cohort included 622 patients (n = 240 in the trial-like cohort). In the main cohort, the median age was 78 years, 77.8% were male, 21.4% were immunocompromised/immunosuppressed, and 63.8% had metastatic CSCC. Median (95% CI) TTD and TTNT were 8.0 (6.6-9.0) months and 16.4 (13.3-21.0) months, respectively, in the main cohort. Median (95% CI) OS was 24.8 (21.8-29.1) months in the main cohort (not reached in the trial-like cohort). In multivariable analyses, age <60 years (hazard ratio & Oslash;], 0.37), Eastern Cooperative Oncology Group performance status <3-4 (HR range, 0.13-0.57), and primary CSCC location in the head and neck only versus extremities only (HR, 0.59) were associated with better OS. Similar OS was observed between patients who had immunosuppressing/immunocompromising conditions and those without. Conclusion: These findings confirm the effectiveness of cemiplimab among a heterogenous, real-world advanced CSCC patient population and substantiate the efficacy of cemiplimab observed in clinical trials.
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收藏
页码:841 / 854
页数:14
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