Biscontini Giuseppina, Romagnolo Cinzia, Cottignoli Chiara, Palucci Andrea, Fringuelli Fabio Massimo, Caldarella Carmelo, Ceci Francesco, Burroni Luca
Department of Nuclear Medicine, "Ospedali Riuniti" Hospital, 60126 Ancona, Italy.
Department of Nuclear Medicine, Fondazione Policlinico "A.Gemelli" IRCCS, 00168 Rome, Italy.
Diagnostics (Basel). 2021 Feb 13;11(2):304. doi: 10.3390/diagnostics11020304.
to explore the diagnostic accuracy of 18F-Fluciclovine positron-emission tomography (PET) in prostate cancer (PCa), considering both primary staging prior to radical therapy, biochemical recurrence, and advanced setting.
A systematic web search through Embase and Medline was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. Studies performed from 2011 to 2020 were evaluated. The terms used were "PET" or "positron emission tomography" or "positron emission tomography/computed tomography" or "PET/CT" or "positron emission tomography-computed tomography" or "PET-CT" and "Fluciclovine" or "FACBC" and "prostatic neoplasms" or "prostate cancer" or "prostate carcinoma". Only studies reporting about true positive (TP), true negative (TN), false positive (FP) and false negative (FN) findings of 18F-fluciclovine PET were considered eligible.
Fifteen out of 283 studies, and 697 patients, were included in the final analysis. The pooled sensitivity for 18F-Fluciclovine PET/CT for diagnosis of primary PCa was 0.83 (95% CI: 0.80-0.86), the specificity of 0.77 (95% CI: 0.74-0.80). The pooled sensitivity for preoperative LN staging was 0.57 (95% CI: 0.39-0.73) and specificity of 0.99 (95% CI: 0.94-1.00). The pooled sensitivity for the overall detection of recurrence in relapsed patients was 0.68 (95% CI: 0.63-0.73), and specificity of 0.68 (95% CI: 0.60-0.75).
This meta-analysis showed promising results in term of sensitivity and specificity for 18F-Fluciclovine PET/CT to stage the primary lesion and in the assessment of nodal metastases, and for the detection of PCa locations in the recurrent setting. However, the limited number of studies and the broad heterogeneity in the selected cohorts and in different investigation protocols are limitation affecting the strength of these results.
探讨18F-氟代脱氧胸苷正电子发射断层扫描(PET)在前列腺癌(PCa)中的诊断准确性,涵盖根治性治疗前的初始分期、生化复发及晚期情况。
根据系统评价和Meta分析的首选报告项目(PRISMA)指南,通过Embase和Medline进行系统的网络检索。对2011年至2020年开展的研究进行评估。使用的检索词为“PET”或“正电子发射断层扫描”或“正电子发射断层扫描/计算机断层扫描”或“PET/CT”或“正电子发射断层扫描-计算机断层扫描”或“PET-CT”以及“氟代脱氧胸苷”或“FACBC”和“前列腺肿瘤”或“前列腺癌”或“前列腺癌”。仅纳入报告18F-氟代脱氧胸苷PET真阳性(TP)、真阴性(TN)、假阳性(FP)和假阴性(FN)结果的研究。
283项研究中的15项及697例患者纳入最终分析。18F-氟代脱氧胸苷PET/CT诊断原发性PCa的合并敏感性为0.83(95%CI:0.80 - 0.86),特异性为0.77(95%CI:0.74 - 0.80)。术前淋巴结分期的合并敏感性为0.57(95%CI:0.39 - 0.73),特异性为0.99(95%CI:0.94 - 1.00)。复发患者总体复发检测的合并敏感性为0.68(95%CI:0.63 - 0.73),特异性为0.68(95%CI:0.60 - 0.75)。
该Meta分析显示,18F-氟代脱氧胸苷PET/CT在对原发性病变进行分期、评估淋巴结转移以及检测复发情况下PCa位置方面,在敏感性和特异性方面取得了有前景的结果。然而,研究数量有限以及所选队列和不同研究方案中存在广泛的异质性是影响这些结果强度的局限性因素。