Publication date: Jul 05, 2025
Non-melanoma skin cancers (NMSC) are the most common malignancies worldwide. While early-stage lesions can be definitively treated with local therapies, advanced stage cutaneous squamous cell carcinoma (cSCC) often requires systemic treatments such as PD-1 inhibitors. These treatments may be administered for prolonged durations; this practice may lead to an unnecessary physical and financial toxicity. The purpose of this study was to evaluate the patterns of disease progression after anti-PD-1 therapy discontinuation in this group of patients. This retrospective cohort study included patients diagnosed with advanced cSCC and treated with either cemiplimab or pembrolizumab from 2019 to 2024 at a single university-affiliated tertiary medical center. The cohort included 131 patients, with a 73% overall response rate. Among the 86 patients with either partial or complete response as the best response included in the final analysis, 40 (47%) patients had a treatment break for at least 3 months, and 46 (53%) continued without discontinuation to a maximal duration of 2 years. After a median follow-up of 29. 9 months, 24 (60%) patients in the break group remained progression-free, systemic treatment-free, and alive throughout the follow-up. Four patients (10%) experienced disease progression. Among these, the best overall response was PR in three patients and CR in one patient. Nine (22. 5%) patients died due to non-oncological reasons, two (5%) patients died from an unknown cause, and one (2. 5%) due to treatment toxicity. The percentage of patients achieving CR was statistically significantly higher in the break group compared to the no-break group. Our findings advocate for a more tailored approach to the duration of PD-1 inhibitor therapy in cSCC, potentially reducing burdens of overtreatment. Future studies regarding establishing robust predictors for safe treatment discontinuation are required to enhance decision-making in clinical practice.
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Semantics
| Type | Source | Name |
|---|---|---|
| disease | MESH | squamous cell carcinoma |
| disease | MESH | melanoma |
| pathway | KEGG | Melanoma |
| disease | MESH | skin cancers |
| disease | MESH | malignancies |
| disease | MESH | disease progression |
| drug | DRUGBANK | Cemiplimab |
| drug | DRUGBANK | Pembrolizumab |
| disease | MESH | overtreatment |
| disease | MESH | morbidity |
| disease | MESH | bleeding |
| disease | MESH | recurrent infection |
| drug | DRUGBANK | Coenzyme M |
| drug | DRUGBANK | Trestolone |
| disease | MESH | sequelae |
| disease | MESH | death |
| disease | MESH | tics |
| drug | DRUGBANK | Honey |
| disease | MESH | chronic renal failure |
| drug | DRUGBANK | Corticorelin |
| disease | MESH | COPD |