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Comprehensive analysis of spread through air spaces in lung adenocarcinoma and squamous cell carcinoma using the 8th edition AJCC/UICC staging system

机译:第8版AJCC / UICC分期系统综合分析肺腺癌和鳞状细胞癌的蔓延

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摘要

Abstract Background This study aimed to comprehensively investigate the effect of spread through air spaces (STAS) on clinicopathologic features, molecular characteristics, immunohistochemical expression, and prognosis in lung adenocarcinomas (ADC) and squamous cell carcinomas (SQCC) based on the 8th edition AJCC/UICC staging system. Methods In total, 303 ADC and 121 SQCC cases were assessed retrospectively. Immunohistochemical staining was performed for E-cadherin, vimentin, Ki67, survivin, Bcl-2, and Bim. Correlations between STAS and other parameters were analyzed statistically. Results STAS was observed in 183 (60.4%) ADC and 39 (32.2%) SQCC cases. In ADC, the presence of STAS was associated with wild-type EGFR, ALK and ROS1 rearrangements, low E-cadherin expression, and high vimentin and Ki67 expression. In SQCC, STAS was associated with low E-cadherin expression and high vimentin and survivin expression. Based on univariate analysis, STAS was associated with significantly shorter disease-free survival (DFS) and overall survival (OS) in ADC. In SQCC, STAS tended to be associated with shorter OS. By multivariate analysis, STAS was an independent poor prognostic factor in ADC for DFS but not OS. Stratified analysis showed that STAS was correlated with shorter DFS for stage I, II, IA, IB, and IIA ADC based on univariate analysis and was an independent risk factor for DFS in stage I ADC cases based on multivariate analysis. Conclusions Our findings revealed that STAS is an independent negative prognostic factor for stage I ADC using the new 8th edition AJCC/UICC staging system. Stage I patients with STAS should be followed up more closely and might need different treatment strategies.
机译:摘要背景本研究旨在全面调查通过空气空间(STA)对肺腺癌(ADC)和鳞状细胞癌(SQCC)的临床病理特征,分子特征,免疫组织化学表达和预后的影响的影响。基于第8版AJCC / UICC分期系统。回顾性地评估总,303ADC和121 SQCC病例的方法。对E-Cadherin,Vimentin,Ki67,Survivin,Bcl-2和BIM进行免疫组织化学染色。统计上分析STA和其他参数之间的相关性。结果在183(60.4%)ADC和39(32.2%)SQCC案件中观察到STA。在ADC中,STA的存在与野生型EGFR,ALK和ROS1重排,低E-Cadherin表达和高Vimentin和Ki67表达相关。在SQCC中,STA与低E-Cadherin表达和高Vimentin和Survivin表达有关。基于单变量分析,STA与ADC中的无病生存期(DFS)和总存活(OS)显着较短。在SQCC中,STA往往与较短的操作系统相关联。通过多变量分析,STA是ADC的独立差的预后因子,用于DFS但不是OS。分层分析表明,基于单变量分析,STA与阶段I,II,IA,IB和IIA ADC的较短DFS相关,并且是基于多变量分析的ADC病例中DFS的独立危险因素。结论我们的调查结果显示,使用新的第8版AJCC / UICC分期系统,STA是I ADC的独立负预后因素。 I阶段,STA患者应更加紧密跟进,可能需要不同的治疗策略。

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