多分期研究可能不会改变高级别发育不良或早期食管腺癌患者的治疗方法。

A Reyhani, E Gimson, C Baker, M Kelly, N Maisey, J Meenan, M Subesinghe, M Hill, J Lagergren, J Gossage, S Zeki, J Dunn, A Davies
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引用次数: 0

摘要

对食管高度发育不良或早期腺癌进行多分期研究的临床价值尚不清楚。分析了2000年至2019年间接受早期食管癌症治疗的单中心前瞻性队列患者。这与食管切除术向内镜黏膜切除术(EMR)的过渡期相吻合。采用计算机断层扫描(CT)、内镜超声(EUS)和2-脱氧-2-[18F]氟代葡萄糖(FDG)正电子发射断层扫描(PET)/CT对患者进行分期。本研究的目的是评估其准确性和对临床管理的影响。297名患有高度发育不良或早期腺癌的患者被纳入研究(内镜治疗/EMR n=184;食管切除术n=113[其中“联合”组在内镜治疗之前进行了手术n=23])。分期准确率低(准确分期EMR:CT 40.1%,EUS 29.6%,FDG-PET/CT 11.0%;食管切除术:CT 43.3%,EUS 59.7%,FDG-PET/CT 29.6%;合并:CT 28.6%,EUS46.2%,FDG-PET/CT 30.0%)。所有可能因T2疾病缺失而改变管理的组的分期不准确率为CT 12%,EUS为12%,FDG-PET/CT为1.6%。所有检测淋巴结疾病的技术的敏感性均较低(CT为12.5%,EUS为12.5%,FDG-PET/CT0.0%)。总体而言,仅3.2%的早期癌症患者在CT和低风险组织学上改变了FDG-PET/CT和EUS的决策。EUS、CT和FDG-PET/CT在食管高度发育不良或早期腺癌患者中的分期准确性较低。在极少数情况下,EUS和FDG-PET/CT比标准CT增加了相关的分期信息,因此,这些研究应选择性使用。预测需要食管切除术的因素主要来自EMR组织学,而不是分期研究。
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Multiple staging investigations may not change management in patients with high-grade dysplasia or early esophageal adenocarcinoma.

The clinical value of multiple staging investigations for high-grade dysplasia or early adenocarcinoma of the esophagus is unclear. A single-center prospective cohort of patients treated for early esophageal cancer between 2000 and 2019 was analyzed. This coincided with a transition period from esophagectomy to endoscopic mucosal resection (EMR) as the treatment of choice. Patients were staged with computed tomography (CT), endoscopic ultrasound (EUS) and 2-deoxy-2-[18F]fluoro-d-glucose (FDG) positron emission tomography(PET)/CT. The aim of this study was to assess their accuracy and impact on clinical management. 297 patients with high-grade dysplasia or early adenocarcinoma were included (endoscopic therapy/EMR n = 184; esophagectomy n = 113 [of which a 'combined' group had surgery preceded by endoscopic therapy n = 23]). Staging accuracy was low (accurate staging EMR: CT 40.1%, EUS 29.6%, FDG-PET/CT 11.0%; Esophagectomy: CT 43.3%, EUS 59.7%, FDG-PET/CT 29.6%; Combined: CT 28.6%, EUS46.2%, FDG-PET/CT 30.0%). Staging inaccuracies across all groups that could have changed management by missing T2 disease were CT 12%, EUS 12% and FDG-PET/CT 1.6%. The sensitivity of all techniques for detecting nodal disease was low (CT 12.5%, EUS 12.5%, FDG-PET/CT0.0%). Overall, FDG-PET/CT and EUS changed decision-making in only 3.2% of patients with an early cancer on CT and low-risk histology. The accuracy of staging with EUS, CT and FDG-PET/CT in patients with high-grade dysplasia or early adenocarcinoma of the esophagus is low. EUS and FDG-PET/CT added relevant staging information over standard CT in very few cases, and therefore, these investigations should be used selectively. Factors predicting the need for esophagectomy are predominantly obtained from EMR histology rather than staging investigations.

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