Takamochi Kazuya, Yoshida Junji, Murakami Koji, Niho Seiji, Ishii Genichiro, Nishimura Mitsuyo, Nishiwaki Yutaka, Suzuki Kazuya, Nagai Kanji
Department of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Lung Cancer. 2005 Feb;47(2):235-42. doi: 10.1016/j.lungcan.2004.08.004.
The evidence of clinical value of positron emission tomography (PET) with fluorine-18 fluorodeoxyglucose (FDG) in lymph node (LN) staging in non-small cell lung cancer (NSCLC) has been shown in numerous papers. However, few studies have assessed its limitations. The aim of the present study is to clarify clinico-pathologic factors responsible for false PET results.
From July 2000 through December 2001, 71 NSCLC patients underwent both FDG PET and surgical intervention at the National Cancer Center Hospital East, Chiba. Clinical records, computed tomographic (CT) scan findings, PET findings, and histologic findings were retrospectively reviewed.
Sensitivity, specificity, accuracy in nodal staging for CT were 29, 83, and 65% and for PET were 39, 79, and 66%, respectively. There were 10 (14%) false-positive PET scans and 14 (20%) false-negative PET scans. The causative factors for false-positive PET scan were: (1) inflammatory conditions in seven patients; (2) PET mis-localization of an interlobar LN as a mediastinal LN in one patient; (3) inability to distinguish the endobronchial polypoid growth of a primary tumor from a lobar LN in one patient; (4) unknown in one patient. All false-positive LNs due to inflammatory conditions showed reactive lymphoid hyperplasia histologically. The causative factors for false-negative PET scan were: (1) limitation of spatial resolution of the PET scanner in 12 patients (maximum tumor focus dimensions in false-negative LNs ranging from 1 to 7.5 mm, with an average of 3.4 mm); (2) PET mis-localization of a mediastinal LN as a hilar LN in one patient; (3) weak FDG uptake by microscopic tumor foci due to necrosis with massive bleeding in a metastatic LN in one patient.
Inflammatory conditions were most responsible for false-positive PET scans, and spatial resolution limitation of FDG PET was the causative factor of false-negative PET scans. Recognizing these factors in advance would be clinically helpful in accurate nodal staging with FDG PET.
众多论文已表明,采用氟 - 18氟脱氧葡萄糖(FDG)的正电子发射断层扫描(PET)在非小细胞肺癌(NSCLC)淋巴结(LN)分期中的临床价值。然而,很少有研究评估其局限性。本研究的目的是阐明导致PET结果出现假阳性的临床病理因素。
2000年7月至2001年12月期间,71例NSCLC患者在千叶县国立癌症中心东医院接受了FDG PET检查和外科手术。对临床记录、计算机断层扫描(CT)结果、PET结果和组织学结果进行回顾性分析。
CT在淋巴结分期中的敏感性、特异性和准确性分别为29%、83%和65%,PET的分别为39%、79%和66%。PET扫描有10例(14%)假阳性和14例(20%)假阴性。PET扫描假阳性的原因有:(1)7例患者存在炎症;(2)1例患者PET将叶间淋巴结误定位为纵隔淋巴结;(3)1例患者无法区分原发性肿瘤的支气管内息肉样生长与叶淋巴结;(4)1例患者原因不明。所有因炎症导致的假阳性淋巴结在组织学上均显示反应性淋巴样增生。PET扫描假阴性的原因有:(1)12例患者PET扫描仪空间分辨率受限(假阴性淋巴结中最大肿瘤灶直径为1至7.5毫米,平均为3.4毫米);(2)1例患者PET将纵隔淋巴结误定位为肺门淋巴结;(3)1例患者转移淋巴结因坏死伴大量出血,微小肿瘤灶FDG摄取较弱。
炎症是PET扫描假阳性的主要原因,FDG PET的空间分辨率受限是PET扫描假阴性的原因。提前认识到这些因素在临床上有助于利用FDG PET进行准确的淋巴结分期。