Department of Pulmonology, Isala Klinieken, Groot Wezenland 20, 8011 JW Zwolle, The Netherlands.
Lung Cancer. 2009 Nov;66(2):198-204. doi: 10.1016/j.lungcan.2009.01.013. Epub 2009 Feb 20.
After induction treatment restaging of mediastinal disease in patients with stage III non-small cell lung cancer (NSCLC) may lead to selection of candidates for further surgical treatment. Nodal down-staging is the best predictive characteristic for proceeding with surgery. We report our experience in restaging with endoscopic ultrasound-guided fine needle aspirations (EUS-FNA) and with repeated integrated positron emission tomography and computed tomography (PET-CT).
Twenty-eight patients with stage III NSCLC were staged with integrated PET-CT, cerebral magnetic resonance imaging (MRI) and pathologically proven nodal disease. Restaging was performed with PET-CT and EUS-FNA on the same nodes that showed initially metastatic disease provided these nodal sites determined the tumor stage. Cerebral MRI was not repeated. When restaging EUS-FNA revealed no malignant cells anymore, patients were operated. The postoperative pathologic results were compared with the preoperative restaging EUS-FNA results. Also, patterns of decreased fluoro-2-deoxyglucose (FDG) uptake were compared with the postoperative pathologic results.
Restaging EUS-FNA was well tolerated in all patients even in those with clinical signs of radiation esophagitis. Of the 28 patients 15 were down-staged based on cytologic findings with restaging EUS-FNA and in one patient the cytology was not conclusive. Of these 15 patients, down-staging was histologically confirmed after mediastinal exploration in 11 patients and 1 patient had persistent nodal disease at resection. In 3 patients no mediastinal tissue verification was performed. Two subjects were not fit for operation, and in the other patient intraoperative nodal staging was omitted. The negative predictive value for restaging EUS-FNA was 91.6%. The accuracy of EUS-FNA was 92.3%. Concordance between findings of restaging EUS-FNA and metabolic response of lymph node metastases occurred in 17 out of 27 patients.
Restaging with EUS-FNA after induction chemo(-radiotherapy) is well tolerated and predicts the absence of nodal metastasis reliably. Although changes in mediastinal FDG-PET uptake show a high concordance with EUS-FNA, pathological confirmation is still superior and therefore necessary. EUS-FNA is the procedure of first choice for mediastinal restaging.
诱导治疗后,III 期非小细胞肺癌(NSCLC)患者纵隔疾病的再分期可能会选择进一步手术治疗的候选者。淋巴结降级是进行手术的最佳预测特征。我们报告了内镜超声引导下细针抽吸术(EUS-FNA)和重复整合正电子发射断层扫描和计算机断层扫描(PET-CT)在再分期中的经验。
28 例 III 期 NSCLC 患者采用整合 PET-CT、脑磁共振成像(MRI)和经病理证实的淋巴结疾病进行分期。再分期采用 PET-CT 和 EUS-FNA 对最初显示转移疾病的相同淋巴结进行,如果这些淋巴结部位确定肿瘤分期,则进行再分期。未重复进行脑 MRI。当再分期 EUS-FNA 显示不再有恶性细胞时,患者接受手术。将术后病理结果与术前再分期 EUS-FNA 结果进行比较。此外,还比较了氟代 2-脱氧葡萄糖(FDG)摄取减少的模式与术后病理结果的关系。
所有患者均能耐受再分期 EUS-FNA,即使有放射性食管炎的临床征象。28 例患者中,15 例根据再分期 EUS-FNA 的细胞学结果降期,1 例细胞学结果不确定。在这 15 例患者中,11 例纵隔探查证实降期,1 例患者切除时仍有淋巴结疾病,3 例患者未进行纵隔组织验证。2 例患者不适合手术,另 1 例患者术中省略了淋巴结分期。再分期 EUS-FNA 的阴性预测值为 91.6%。EUS-FNA 的准确性为 92.3%。27 例患者中有 17 例再分期 EUS-FNA 与淋巴结转移代谢反应之间的结果一致。
诱导化疗(放化疗)后 EUS-FNA 再分期耐受性良好,可靠地预测淋巴结无转移。尽管纵隔 FDG-PET 摄取的变化与 EUS-FNA 具有高度一致性,但病理证实仍具有优势,因此是必要的。EUS-FNA 是纵隔再分期的首选方法。