Harders Stefan Walbom, Madsen Hans Henrik, Hjorthaug Karin, Arveschoug Anne Kirstine, Rasmussen Torben Riis, Meldgaard Peter, Hoejbjerg Johanne Andersen, Pilegaard Hans Kristian, Hager Henrik, Rehling Michael, Rasmussen Finn
Cancer Imaging. 2014 Jun 3;14(1):23. doi: 10.1186/1470-7330-14-23.
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.
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.
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.
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.
在确诊为非小细胞肺癌(NSCLC)后,必须考虑疾病的分期,因为这将直接影响治疗和预后。分期用于预测生存率,并指导患者选择最合适的治疗方案或临床试验。区分纵隔淋巴结(N2或N3)与肺门淋巴结或无淋巴结转移(N0或N1)的恶性受累情况至关重要,因为N2或N3淋巴结的恶性受累通常表明疾病无法手术切除。本研究的目的是检查和比较CT与F18-FDG PET/低剂量CT(FDG PET/CT)在NSCLC纵隔分期中的应用,希望在无需侵入性操作的情况下安全地区分恶性和良性病变。所有结果均进行了可重复性控制。
114例NSCLC患者纳入前瞻性队列研究。对CT和FDG PET/CT图像进行盲法评估。根据淋巴结大小(CT)或FDG摄取情况(FDG PET/CT)对患者的纵隔进行分期。参考标准为组织取样。
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;总体而言,研究中三分之二的患者分期正确,近三分之一的患者分期错误。
对于NSCLC患者,CT和FDG PET/CT均不能避免在开胸手术前进行进一步侵入性分期的需要;为此,两种检查方法的结果都不太理想。因此,这些患者仍依赖侵入性分期方法。在我们的研究中,侵入性分期通过纵隔镜检查完成。然而,如今这一方法越来越多地被超声支气管镜(EBUS)或超声内镜(EUS)所取代。