Efficacy of Cemiplimab as Adjuvant or Neoadjuvant Therapy in the Treatment of Cutaneous Squamous Cell Carcinoma

被引:0
作者
Hiller, Andrea [1 ]
Oxford, Madison [2 ]
Kulkarni, Pallavi [2 ]
Fornadley, Jeffrey [3 ]
Lo, Alexis [1 ]
Sivik, Jeffrey [4 ]
Drabick, Joseph [5 ]
Vakharia, Kavita [1 ]
机构
[1] Penn State Hlth Milton S Hershey, Dept Surg, Div Plast Surg, 500 Univ Dr,MC H071, Hershey, PA 17033 USA
[2] Penn State Coll Med, Hershey, PA USA
[3] Penn State Hlth Med Grp Riverfront Plast Surg, Harrisburg, PA USA
[4] Penn State Hershey Med Ctr, Dept Pharm, Hershey, PA USA
[5] Penn State Hershey Med Ctr, Dept Med, Div Hematol Oncol, Hershey, PA USA
关键词
cutaneous squamous cell carcinoma; immunotherapy; neoadjuvant therapy; adjuvant therapy; REAL-WORLD DATA; DEATH;
D O I
10.1097/SAP.0000000000003847
中图分类号
R61 [外科手术学];
学科分类号
摘要
IntroductionCutaneous squamous cell carcinoma (cSCC) is the second most common skin cancer in the White population. Unfortunately, the prognosis of advanced cSCC is poor, and management can be challenging. Until recently, the choice of systemic medications was limited, and those that were available had modest efficacy. Cemiplimab is an anti-programmed cell-death protein 1 inhibitor and the first immunotherapeutic agent approved for the treatment of metastatic or locally advanced cSCC. The purpose of this study was to evaluate the efficacy of cemiplimab when used as adjuvant or neoadjuvant therapy in patients treated at our institution.MethodsA retrospective review of patients with locally advanced or metastatic cSCC who were treated with cemiplimab as adjuvant or neoadjuvant therapy at a single institution between February 2019 and November 2022 was performed. Response to treatment was objectively assessed based on Response Evaluation Criteria in Solid Tumors, version 1.1, criteria. The primary end point was objective response rate. Secondary endpoints included time to observed response, disease-control rate, progression-free survival, overall survival, and adverse effects of therapy.ResultsA total of 6 patients were identified with a median age of 79 years (range, 51-90 years). Four patients had locally advanced cSCC, and 2 had distant metastasis. Cemiplimab was used as adjuvant therapy in 3 patients and neoadjuvant therapy in 2 patients. There was 1 patient in which it was used for limb salvage, who would have otherwise required an amputation. Objective response rate, complete response, and partial response were 66% (4 of 6), 33% (2 of 6), and 33% (2 pf 6), respectively. Average time to observed response was 2.9 months. Disease-control rate was 83% (5 of 6), and average progression-free survival was 10 months. Toxicity was reported in 2 patients, both of which were grade 1 severity.ConclusionsCemiplimab has established its utility in the treatment of advanced cSCC, demonstrating clinical efficacy while generally having a tolerable adverse effect profile. Our preliminary results suggest that cemiplimab has potential as an adjuvant or neoadjuvant therapy in combination with surgery for treatment of cSCC.
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页码:S129 / S131
页数:3
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