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Mediastinal staging in non-small-cell lung carcinoma: computed tomography versus F-18-fluorodeoxyglucose positron-emission tomography and computed tomography

机译:非小细胞肺癌的纵隔分期:计算机断层扫描与F-18-氟脱氧葡萄糖正电子发射断层扫描和计算机断层扫描

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Background After the diagnosis Non-Small-Cell Lung Carcinoma ( NSCLC ) has been established, consideration must turn toward the stage of disease, because this will impact directly on management and prognosis. Staging is used to predict survival and to guide the patient toward the most appropriate treatment regimen or clinical trial. Distinguishing malignant involvement of the mediastinal lymph nodes (N2 or N3) from the hilar lymph nodes, or no lymph nodes (N0 or N1) is critical, because malignant involvement of N2 or N3 lymph nodes usually indicates non – surgically resectable disease. The purpose of this study was to examine and compare CT versus integrated F18-FDG PET/low dose CT ( FDG PET / CT ) for mediastinal staging in NSCLC, and the desire was to safely distinguish between malignant and benign lesions without the need for invasive procedures. All results were controlled for reproducibility. Methods 114 participants with NSCLC were included in a prospective cohort study. Blinded CT and FDG PET/CT images were reviewed. The participants’ mediastinums were staged based on lymph node sizes (CT), or on FDG uptake (FDG PET/CT). Reference standard was tissue sampling. Results We found that there was no measureable difference between CT and FDG PET/CT mediastinal staging results; overall two-thirds of the participants in the study were correctly staged, and almost one-third of the participants were falsely staged. Conclusion Neither CT nor FDG PET/CT could obviate the need for further invasive staging prior to thoracotomy in patients with NSCLC; for that purpose, the results of both modalities were too meagre. Therefore, these patients still depend on invasive staging methods. In our study, invasive staging was accomplished by mediastinoscopy. However, today this is increasingly replaced by EBUS or EUS.
机译:背景诊断非小细胞肺癌(NSCLC)确立后,必须考虑疾病的发展阶段,因为这将直接影响治疗和预后。分期用于预测生存率并指导患者进行最合适的治疗方案或临床试验。区分纵隔淋巴结(N2或N3)与肺门淋巴结是否恶变或无淋巴结(N0或N1)是至关重要的,因为N2或N3淋巴结的恶性累及通常表示不可手术切除的疾病。这项研究的目的是检查和比较CT与F18-FDG PET /低剂量CT(FDG PET / CT)在非小细胞肺癌纵隔分期中的应用,并且希望能够安全地区分恶性和良性病变而无需侵入性程序。控制所有结果的可重复性。方法将114例NSCLC参与者纳入一项前瞻性队列研究。审查了盲CT和FDG PET / CT图像。根据淋巴结大小(CT)或FDG摄取量(FDG PET / CT)对参与者的纵隔进行分期。参考标准是组织采样。结果我们发现CT和FDG PET / CT纵隔分期结果之间没有可测量的差异。整个研究中有三分之二的参与者正确上演,几乎三分之一的参与者被错误地上演。结论CT和FDG PET / CT均不能避免NSCLC患者在开胸手术前进行进一步的侵入性分期。为此,两种方法的结果都太微不足道了。因此,这些患者仍然依赖于侵入性分期方法。在我们的研究中,侵入性分期是通过纵隔镜完成的。但是,如今,这已越来越被EBUS或EUS取代。

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