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经抗 PD-1 免疫治疗的皮肤鳞状细胞癌:通过 F-FDG 连续 PET/CT 扫描监测反应。

Cutaneous Squamous Cell Carcinoma Subjected to Anti PD-1 Immunotherapy: Monitoring Response Through Serial PET/CT Scans with F-FDG.

机构信息

Department of Nuclear Medicine, Santa Maria Goretti Hospital, Latina, Italy.

Dermatology Unit "Daniele Innocenzi," "A. Fiorini" Hospital, Terracina, Italy.

出版信息

Cancer Biother Radiopharm. 2022 Apr;37(3):226-232. doi: 10.1089/cbr.2021.0368. Epub 2022 Feb 4.

DOI:10.1089/cbr.2021.0368
PMID:35128935
Abstract

The effectiveness of F-fluorodeoxyglucose (F-FDG) positron emission computed tomography (PET/CT) for monitoring response to immunotherapy (IT) with cemiplimab in patients affected by cutaneous squamocellular carcinoma (cSCC) was investigated. Thirteen cSCC patients performed PET/CT at baseline (PET-1) and 3 months after IT (PET-2). According to immune PET Response Criteria in Solid Tumors (iPERCIST), patients showing progressive disease at PET-2 were classified as having "unconfirmed progressive metabolic disease" (uPMD) and were scheduled to perform a further PET/CT (PET-3) after 4 weeks. PET/CT's results were correlated with best clinical response (BCR) categorized, within 6 months from the start of IT, as clinical benefit (CB) or no clinical benefit (NCB) according to clinical follow-up. At PET-2, 9 subjects (69.2%) showed metabolic response, whereas four (30.8%) were classified as uPMD. After 4 weeks, three uPMD patients were subjected to PET-3, which confirmed progressive disease in all cases, whereas 1 patient with uPMD did not undergo PET-3 due to clinical deterioration. All subjects with metabolic response at PET-2 were classified as having CB and continued IT in 8 out of 9 cases, whereas all patients with uPMD were categorized as NCB and discontinued IT. PET/CT, performed in cSCC patients after 3 months of cemiplimab, resulted capable to identify responders from nonresponders.

摘要

研究了 F-氟代脱氧葡萄糖(F-FDG)正电子发射计算机断层扫描(PET/CT)在监测接受西米普利单抗免疫治疗(IT)的皮肤鳞状细胞癌(cSCC)患者反应中的有效性。13 例 cSCC 患者在基线(PET-1)和 IT 后 3 个月(PET-2)进行了 PET/CT 检查。根据实体瘤免疫 PET 反应标准(iPERCIST),PET-2 显示疾病进展的患者被归类为“未确认的进行性代谢疾病”(uPMD),并计划在 4 周后进行进一步的 PET/CT(PET-3)。将 PET/CT 的结果与最佳临床反应(BCR)相关联,在 IT 开始后 6 个月内,根据临床随访将其归类为临床获益(CB)或无临床获益(NCB)。在 PET-2 时,9 名受试者(69.2%)显示代谢反应,而 4 名受试者(30.8%)被归类为 uPMD。4 周后,3 名 uPMD 患者接受了 PET-3,所有病例均证实疾病进展,而 1 名 uPMD 患者因临床恶化未接受 PET-3。PET-2 时代谢反应的所有受试者均被归类为 CB,并在 8 例中的 9 例中继续接受 IT,而所有 uPMD 患者均被归类为 NCB 并停止接受 IT。在接受西米普利单抗治疗 3 个月后的 cSCC 患者中进行的 PET/CT 能够识别出应答者和无应答者。

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引用本文的文献

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Clin Cosmet Investig Dermatol. 2023 Aug 9;16:2135-2142. doi: 10.2147/CCID.S381471. eCollection 2023.
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The Role and Potential of F-FDG PET/CT in Malignant Melanoma: Prognostication, Monitoring Response to Targeted and Immunotherapy, and Radiomics.F-FDG PET/CT在恶性黑色素瘤中的作用及潜力:预后评估、监测靶向治疗和免疫治疗反应以及放射组学
Diagnostics (Basel). 2022 Apr 8;12(4):929. doi: 10.3390/diagnostics12040929.