Clinical outcomes following PD-1 inhibitor elective discontinuation in cutaneous squamous cell carcinoma: exploring treatment de-escalation.

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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Concepts Keywords
9months Adult
Carcinoma Aged
Free Aged, 80 and over
Therapy Anti-PD-1 therapy discontinuation
University Antibodies, Monoclonal, Humanized
Antibodies, Monoclonal, Humanized
Carcinoma, Squamous Cell
cemiplimab
Female
Humans
Immune Checkpoint Inhibitors
Immune Checkpoint Inhibitors
Male
Middle Aged
PD-1 inhibitors
PDCD1 protein, human
pembrolizumab
Retrospective Studies
Skin Neoplasms
Treatment Outcome
Withholding Treatment

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

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