[18F]FDG PET/CT对接受西咪咪单抗免疫治疗的晚期皮肤鳞状细胞癌患者的预后作用:一项单中心回顾性研究。

IF 2.4 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Cancer Biotherapy and Radiopharmaceuticals Pub Date : 2024-02-01 Epub Date: 2023-10-26 DOI:10.1089/cbr.2023.0110
Luca Filippi, Ilaria Proietti, Vincenzo Petrozza, Concetta Potenza, Oreste Bagni, Orazio Schillaci
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引用次数: 0

摘要

背景:研究了基线2-脱氧-2[18F]氟代葡萄糖([18F]FDG)正电子发射断层扫描(PET)衍生的参数和12周的代谢反应,作为晚期皮肤鳞状细胞癌(cSCC)接受头孢单抗免疫治疗的预后因素。材料和方法:回顾性回顾25例接受西米普利单抗治疗的cSCC患者在基线和~12周后接受[18F]FDG正电子发射断层扫描/计算机断层扫描(PET/CT)的临床记录。Kaplan-Meier(KM)方法用于分析无事件生存率(EFS)的差异,Cox回归分析用于确定预后因素。结果:在12周的PET/CT评估中,根据实体瘤免疫PET反应标准(iPERCIST),16名患者(64%)被归类为有反应者(完全或部分有反应),9名患者(36%)为无反应者(“未经证实的进行性代谢疾病”)。通过KM分析,基线代谢肿瘤体积(MTV)和总损伤糖酵解(TLG)与EFS显著相关(p p 结论:基线肿瘤负荷(即MTV和TLG)和12周时的代谢反应可能对接受西米普利单抗治疗的cSCC患者的预后产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

Background: Baseline 2-deoxy-2[18F]fluoro-d-glucose ([18F]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 [18F]FDG positron emission tomography/computed tomography (PET/CT) at baseline and after ∼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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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
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