The Prognostic Role of [18F]FDG PET/CT in Patients with Advanced Cutaneous Squamous Cell Carcinoma Submitted to Cemiplimab Immunotherapy: A Single-Center Retrospective Study

被引:0
|
作者
Filippi, Luca [1 ]
Proietti, Ilaria [2 ]
Petrozza, Vincenzo [3 ]
Potenza, Concetta [2 ]
Bagni, Oreste [4 ]
Schillaci, Orazio [5 ]
机构
[1] Fdn PTV Policlin Tor Vergata Univ Hosp, Dept Oncohaematol, Nucl Med Unit, Viale Oxford 81, I-00133 Rome, Italy
[2] A Fiorini Hosp, Dermatol Unit Daniele Innocenzi, Terracina, Italy
[3] Univ Roma La Sapienza, ICOT Hosp, Dept Med Surg Sci & Biotechnol, Pathol Unit, Rome, Italy
[4] Santa Maria Goretti Hosp, Nucl Med Unit, Latina, Italy
[5] Univ Tor Vergata, Dept Biomed & Prevent, Rome, Italy
关键词
PET/CT; nuclear medicine; squamous cutaneous carcinoma; precision medicine; oncology; F-18]FDG; immunotherapy; F-18-FDG PET/CT;
D O I
10.1089/cbr.2023.0110
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Baseline 2-deoxy-2[F-18]fluoro-d-glucose ([F-18]FDG) positron emission tomography (PET)-derived parameters and 12-week metabolic response were investigated as prognostic factors in advanced cutaneous squamous cell carcinoma (cSCC) submitted to cemiplimab immunotherapy.Materials and Methods: Clinical records of 25 cSCC patients receiving cemiplimab, submitted to [F-18]FDG positron emission tomography/computed tomography (PET/CT) at baseline and after similar to 12 weeks, were retrospectively reviewed. The Kaplan-Meier (KM) method was applied to analyze differences in event-free survival (EFS), and Cox regression analysis was employed to identify the prognostic factors.Results: At the 12-week PET/CT evaluation, 16 patients (64%) were classified as responders (complete or partial response) and 9 (36%) as nonresponders ("unconfirmed progressive metabolic disease") according to immune PET Response Criteria in Solid Tumors (iPERCIST). By KM analysis, baseline metabolic tumor volume (MTV) and total lesion glycolysis (TLG) significantly correlated with the EFS (p < 0.05). Furthermore, the KM analysis showed that the lack of metabolic response at 12 weeks was associated with meaningfully shorter EFS (7.2 +/- 1 months in nonresponders vs. 20.3 +/- 2.3 months in responders). In Cox multivariate analysis, metabolic response at 12 weeks remained the only predictor of the EFS (p < 0.05).Conclusions: Baseline tumor load (i.e., MTV and TLG) and metabolic response at 12 weeks may have a prognostic impact in cSCC patients treated with cemiplimab.
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页码:46 / 54
页数:9
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