Zamani-Siahkali Nazanin, Mirshahvalad Seyed Ali, Pirich Christian, Beheshti Mohsen
Division of Molecular Imaging and Theranostics, Department of Nuclear Medicine, University Hospital, Paracelsus Medical University, 5020 Salzburg, Austria.
Department of Nuclear Medicine, Shariati Hospital, Tehran University of Medical Sciences, Tehran 1461884513, Iran.
Cancers (Basel). 2024 Jan 2;16(1):215. doi: 10.3390/cancers16010215.
We described the diagnostic performance of [F]F-FDG-PET in malignant melanoma by conducting a comprehensive systematic review and meta-analysis of the existing literature. The study was designed following PRISMA-DTA. Original articles with adequate crude data for meta-analytic calculations that evaluated [F]F-FDG-PET and compared it with a valid reference standard were considered eligible. The pooled measurements were calculated based on the data level (patient/lesion-based). Regarding sub-groups, diagnostic performances were calculated for local, regional and distant involvement. The bivariate model was employed to calculate sensitivity and specificity. The initial search resulted in 6678 studies. Finally, 100 entered the meta-analysis, containing 82 patient-based (10,403 patients) and 32 lesion-based (6188 lesions) datasets. At patient level, overall, [F]F-FDG-PET had pooled sensitivity and specificity of 81% (95%CI: 73-87%) and 92% (95%CI: 90-94%), respectively. To detect regional lymph node metastasis, the pooled sensitivity and specificity were 56% (95%CI: 40-72%) and 97% (95%CI: 94-99%), respectively. To detect distant metastasis, they were 88% (95%CI: 81-93%) and 94% (95%CI: 91-96%), respectively. At lesion level, [F]F-FDG-PET had a pooled sensitivity and specificity of 70% (95%CI: 57-80%) and 94% (95%CI: 88-97%), respectively. Thus, [F]F-FDG-PET is a valuable diagnostic modality for melanoma assessment. It was accurate in various clinical scenarios. However, despite its high specificity, it showed low sensitivity in detecting regional lymph node metastasis and could not replace lymph node biopsy.
我们通过对现有文献进行全面的系统评价和荟萃分析,描述了[F]F-FDG-PET在恶性黑色素瘤中的诊断性能。该研究是按照PRISMA-DTA设计的。纳入标准为具有足够原始数据用于荟萃分析计算的原始文章,这些文章评估了[F]F-FDG-PET并将其与有效的参考标准进行了比较。汇总测量值是根据数据水平(基于患者/病灶)计算得出的。对于亚组,计算了局部、区域和远处受累的诊断性能。采用双变量模型计算敏感性和特异性。初步检索得到6678项研究。最终,100项研究纳入荟萃分析,其中包括82项基于患者的研究(10403例患者)和32项基于病灶的研究(6188个病灶)。在患者层面,总体而言,[F]F-FDG-PET的汇总敏感性和特异性分别为81%(95%CI:73-87%)和92%(95%CI:90-94%)。检测区域淋巴结转移时,汇总敏感性和特异性分别为56%(95%CI:40-72%)和97%(95%CI:94-99%)。检测远处转移时,分别为88%(95%CI:81-93%)和94%(95%CI:91-96%)。在病灶层面,[F]F-FDG-PET的汇总敏感性和特异性分别为70%(95%CI:57-80%)和94%(95%CI:88-97%)。因此,[F]F-FDG-PET是黑色素瘤评估的一种有价值的诊断方法。它在各种临床情况下都很准确。然而,尽管其特异性较高,但在检测区域淋巴结转移方面敏感性较低,不能替代淋巴结活检。