Commentary|Videos|October 28, 2025

Adjuvant Cemiplimab for High-Risk CSCC: Risk Stratification in Practice

Fact checked by: Andrea Eleazar, MHS

Dr Vishal A. Patel explores critical scenarios for using cemiplimab in treating high-risk cutaneous squamous cell carcinoma, enhancing patient outcomes through tailored strategies.

In an interview with Targeted Oncology, Vishal A. Patel, MD, FAAD, FACMS, associate professor of Dermatology and of Medicine (Hematology/Oncology) at George Washington (GW) University School of Medicine and Health Sciences and director, Cutaneous Oncology Program at GW Cancer Center, details 2 scenarios where oncologists should consider the use of cemiplimab, now FDA-approved, in adjuvant treatment of cutaneous squamous cell carcinoma (CSCC).

Watch part 1, part 2, part 3, and part 4 of Dr Patel’s interview.

Case 1 describes a patient with a large primary lesion and suspected lymph node involvement that worsens upon detailed pathology. Initial imaging may suggest only one or two nodes, but final dissection reveals 3 positive lymph nodes, including a node measuring 2 cm, along with facial nerve involvement. Meeting multiple C-POST trial (NCT03969004) criteria, this patient would be recommended for postoperative radiation therapy, with adjuvant cemiplimab strongly advised.

Case 2 highlights the importance of full histologic evaluation, presenting a case where a tumor resection reveals bone invasion or presence of in-transit metastases, constituting high-risk features that put the patient at substantial risk for recurrence.

In part 1 of the interview, Dr Patel emphasized the significance of the intentional selection of inclusion criteria utilized within the C-POST trial, as these may help guide the decision-making process in determining which patients are at high risk for recurrence. In part 2, he also underscored the importance of approaching the treatment decision with a nuanced lens, factoring in patients’ individual circumstances to maximize the benefits of treatment with this agent.

“It is important for the oncologist to consider those nuances, [which] can help improve the outcomes of those patients that may fall through the cracks and have not received off-label neoadjuvant therapy, or those patients that we worry may have a harder time receiving salvage systemic therapy later,” said Dr Patel in the interview.

These cases illustrate scenarios where final pathology often reveals a higher risk of recurrence than anticipated, requiring oncologists to appropriately risk-stratify and apply the C-POST inclusion criteria to determine if patients will benefit from adjuvant cemiplimab.

Read the full interview here.


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