Deng Yueling, Zhang Xiao, Song Yangmeihui, Lan Xiaoli
Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hubei Key Laboratory of Molecular Imaging, Wuhan, China.
Eur Radiol. 2025 Jul 21. doi: 10.1007/s00330-025-11864-y.
This study aimed to systematically compare the efficacy of [F]FDG PET/CT and CT in evaluating the response to immunotherapy in patients with advanced melanoma.
A comprehensive literature search was conducted across PubMed, Embase, Cochrane Library, Web of Science, and ClinicalTrials.gov. The study focused on comparing time-to-event hazard ratios (HRs) between patients categorized as complete response (CR) and non-complete response (non-CR) based on the two imaging assessment modalities. Eligible studies were selected based on the availability of both survival data and appropriate imaging methods, with special attention to the use of CT as part of PET/CT protocols in some cases. Additionally, PET and CT assessments were paired for each individual to analyze the efficacy of these imaging methods in detecting CR, assess the mismatch rate, and identify its causes.
A review of 1445 candidate articles identified 15 eligible studies involving 952 patients. For CR and non-CR patients, the combined HR for PET was 4.10 (95% CI = 2.71-6.19), while for CT it was 1.25 (95% CI = 0.63-2.46). The high rate of PET-/CT+ discordance (48%, 95% CI: 42-53%) indicates that CT frequently misclassifies residual inflammation or fibrosis as active disease, whereas the absence of PET+/CT- cases (0%, 95% CI: 0-3%) highlights the high specificity of PET in detecting true residual tumors.
This evidence supports prioritizing [F]FDG PET/CT over CT for post-immunotherapy assessment of advanced melanoma. In direct comparison with CT, [F]FDG PET/CT demonstrated superior predictive capabilities for immunotherapy response and survival outcomes.
Question How do [F]-FDG PET/CT and CT compare for assessing immunotherapy response and survival prediction in patients with advanced melanoma. Findings Meta-analysis of 15 studies showed [F]-FDG PET/CT (HR = 4.10) had better predictive value than CT (HR = 1.25). Clinical relevance These findings support the prioritization of [F]-FDG PET/CT over CT for post-immunotherapy assessment in advanced melanoma, as it provides more reliable predictions of treatment response and survival outcomes, helping clinicians make more informed therapeutic decisions.
本研究旨在系统比较[F]FDG PET/CT与CT在评估晚期黑色素瘤患者免疫治疗反应方面的疗效。
在PubMed、Embase、Cochrane图书馆、Web of Science和ClinicalTrials.gov上进行了全面的文献检索。该研究重点比较了根据两种成像评估方式分为完全缓解(CR)和非完全缓解(非CR)的患者之间的事件发生时间风险比(HR)。根据生存数据和适当成像方法的可用性选择符合条件的研究,特别注意在某些情况下将CT用作PET/CT方案的一部分。此外,对每个个体的PET和CT评估进行配对,以分析这些成像方法在检测CR方面的疗效,评估不匹配率,并确定其原因。
对1445篇候选文章的回顾确定了15项符合条件的研究,涉及952名患者。对于CR和非CR患者,PET的合并HR为4.10(95%CI=2.71-6.19),而CT为1.25(95%CI=0.63-2.46)。PET-/CT+不一致率较高(48%,95%CI:42-53%),表明CT经常将残留炎症或纤维化误分类为活动性疾病,而PET+/CT-病例不存在(0%,95%CI:0-3%)突出了PET在检测真正残留肿瘤方面的高特异性。
这一证据支持在晚期黑色素瘤免疫治疗后评估中优先选择[F]FDG PET/CT而非CT。与CT直接比较,[F]FDG PET/CT在免疫治疗反应和生存结果的预测能力方面表现更优。
问题:[F]-FDG PET/CT与CT在评估晚期黑色素瘤患者免疫治疗反应和生存预测方面的比较如何。研究结果:对15项研究的荟萃分析表明,[F]-FDG PET/CT(HR=4.10)比CT(HR=1.25)具有更好的预测价值。临床意义:这些发现支持在晚期黑色素瘤免疫治疗后评估中优先选择[F]-FDG PET/CT而非CT,因为它能提供更可靠的治疗反应和生存结果预测,帮助临床医生做出更明智的治疗决策。