18F-FDG PET在早期转移性睾丸精原细胞瘤中的准确性:来自SEMS试验的分析。

Brian Hu,Muhannad Alsyouf,Ala'a Farkouh,Clint Cary,Timothy Masterson,Lawrence Einhorn,Nabil Adra,Stephen A Boorjian,Christian Kollmannsberger,Anne Schuckman,Alan So,Peter C Black,Aditya Bagrodia,Eila Skinner,Mehrdad Alemozaffar,Timothy Brand,Scott Eggener,Phillip Pierorazio,Kelly Stratton,Lucia Nappi,Craig Nichols,Siamak Daneshmand
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引用次数: 0

摘要

目的最近对睾丸精原细胞瘤进行的原发性淋巴结清扫术(RPLND)临床试验凸显了传统影像学在淋巴结分期方面的不准确性。有关化疗无效睾丸精原细胞瘤患者正电子发射断层扫描(PET)准确性的数据有限。我们在 SEMS 试验(早期转移性精原细胞瘤手术)中评估了 18F-FDG PET 检测转移性疾病的准确性。方法SEMS 试验是一项 II 期前瞻性研究,评估了伴有局限性腹膜后淋巴结病变的睾丸精原细胞瘤患者初次 RPLND 的疗效。手术前,除标准轴向成像外,还进行了 18F-FDG PET 扫描作为放射学相关检查。结果 在 55 例参加试验的患者中,26 例(47%)接受了 PET 扫描。20例(77%)扫描结果显示腹膜后、骨盆或腹股沟区淋巴结阳性。在 PET 扫描呈阳性的患者中,18 人在进行 RPLND 时淋巴结呈病理阳性(PPV 90%)。6 例 PET 扫描结果为阴性,其中 5 例经手术确诊为 pN0 病变(NPV 83%)。PET 检测淋巴结转移性精索瘤的敏感性为 95%,特异性为 71%。PET 阳性淋巴结和病理阳性淋巴结的平均 SUV 分别为 7.0(范围 2.6-18.8)和 6.8(范围 1.53-18.8)。结论 在大多数睾丸精原细胞瘤患者中,18F-FDG PET 发现与病理阳性和阴性腹膜后淋巴结相关。还需要进一步研究,以确定 PET 是否能提高传统成像和临床专业知识的良好预测性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Accuracy of 18F-FDG PET in Early Metastatic Testicular Seminoma: Analysis from the SEMS Trial.
PURPOSE Recent clinical trials on primary RPLND for testicular seminoma highlight inaccuracies in conventional imaging for lymph node staging. Limited data exist on the accuracy of positron emission tomography (PET) in patients with chemotherapy-naïve testicular seminoma. We evaluated the accuracy of 18F-FDG PET for detection of metastatic disease within the SEMS trial (Surgery in Early Metastatic Seminoma). METHODS The SEMS trial is a phase II prospective study evaluating efficacy of primary RPLND in patients with testicular seminoma with limited retroperitoneal lymphadenopathy. 18F-FDG PET scanning was performed as a radiographic correlate in addition to standard axial imaging prior to surgery. PET findings were based upon local interpretation and results were compared to surgical pathology. RESULTS Of the 55 patients enrolled in the trial, 26 (47%) underwent PET. Twenty (77%) scans were reported as positive with lymph nodes in the retroperitoneum, pelvis, or inguinal region. Of the positive PET scans, eighteen had pathologically positive lymph nodes (PPV 90%) at time of RPLND. Six PET scans were negative with five of these patients having surgically confirmed pN0 disease (NPV 83%). Sensitivity of PET for detecting lymph node metastatic seminoma was 95% and specificity was 71%. The average SUV of the PET positive lymph nodes and pathologically positive lymph node were 7.0 (range 2.6-18.8) and 6.8 (range 1.53-18.8), respectively. No PET positive lesions outside of the retroperitoneum or pelvis were found to represent metastatic seminoma on clinical follow-up. CONCLUSION In patients with testicular seminoma, 18F-FDG PET findings correlated with both pathologically positive and negative retroperitoneal lymph nodes in the majority of cases. Further research is needed to determine if PET can improve upon the already good predictive performance of conventional imaging and clinical expertise.
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