Taylor Oliver, Boardman Glenn, Bentel Jacqueline, Laycock Andrew
PathWest Anatomical Pathology, Fiona Stanley Hospital, Perth, Western Australia, Australia.
School of Medicine, The University of Notre Dame, Fremantle, Western Australia, Australia.
Asia Pac J Clin Oncol. 2023 Dec;19(6):706-714. doi: 10.1111/ajco.13934. Epub 2023 Jan 27.
This study was performed to evaluate concordance between clinical and pathologic staging of non-small cell lung cancer (NSCLC) in our hospital network.
We retrospectively reviewed records of 417 patients with NSCLC who received curative surgery and whose pathology was evaluated in our hospital between 2016 and 2021. Cytology, tissue pathology, and associated clinical, surgical, and imaging information were retrieved from hospital digital records.
The cohort included 214 female and 203 male patients aged 20.6-85.8 years. Median times among staging computed tomography and surgery (105 days [interquartile range (IQR) 77.0-143.0]), positron emission tomography and surgery (78.5 days [IQR 56.0-109.0]), and endobronchial ultrasound-guided transbronchial needle aspiration and surgery (59 days [IQR 42-94]) indicated that Australian guidelines of <42 days between original referral and commencement of treatment were not being met in the majority of cases. Discordance between clinical TNM (cTNM) and pathologic TNM staging was 25.9%, including 18.4% cases that were clinically understaged and two patients with undetected stage IVA disease. cTNM understaging was significantly associated with time between the final staging investigation and surgery (p = .023), pleural (p < .05) and vessel (p < .05) invasion, and diagnosis of high-grade adenocarcinoma (p = .001).
Discordance between clinical and pathologic staging of NSCLC is associated with tumor histopathologic characteristics and treatment delays. Although tumor factors that lead to discordant staging cannot be controlled, reduced time to surgery may have resulted in better outcomes for some patients in this potentially curable lung cancer cohort.
本研究旨在评估我院网络中非小细胞肺癌(NSCLC)临床分期与病理分期之间的一致性。
我们回顾性分析了2016年至2021年间在我院接受根治性手术且病理得到评估的417例NSCLC患者的记录。从医院数字记录中检索细胞学、组织病理学以及相关的临床、手术和影像信息。
该队列包括214例女性和203例男性患者,年龄在20.6 - 85.8岁之间。分期计算机断层扫描与手术之间的中位时间(105天[四分位间距(IQR)77.0 - 143.0])、正电子发射断层扫描与手术之间的中位时间(78.5天[IQR 56.0 - 109.0])以及支气管内超声引导下经支气管针吸活检与手术之间的中位时间(59天[IQR 42 - 94])表明,在大多数病例中未达到澳大利亚指南中关于初次转诊至开始治疗间隔<42天的标准。临床TNM(cTNM)分期与病理TNM分期之间的不一致率为25.9%,其中18.4%的病例临床分期过低,且有2例患者未检测出IVA期疾病。cTNM分期过低与最终分期检查至手术的时间(p = 0.023)、胸膜(p < 0.05)和血管(p < 0.05)侵犯以及高级别腺癌的诊断(p = 0.001)显著相关。
NSCLC临床分期与病理分期之间的不一致与肿瘤组织病理学特征及治疗延迟有关。虽然导致分期不一致的肿瘤因素无法控制,但缩短手术时间可能使该潜在可治愈肺癌队列中的部分患者获得更好的结局。