Pub Date : 2025-12-31Epub Date: 2025-12-29DOI: 10.21037/jtd-2025-1538
Xi Lin, Jian-Xun Wen, Yan Niu, Hong-Zhe Zhu, Cheng Yan, Su-Na Cha, Wen-Qi Zheng, Zhi-De Hu, Li Yan, Jin-Hong Huang, Hong Chen, Qianghua Zhou, Ting-Wang Jiang, Man Zhang
Background: Neuron-specific enolase (NSE) in pleural fluid has been proposed as a promising diagnostic biomarker. However, existing studies on the diagnostic accuracy of NSE have reported inconsistent results. This study aimed to assess the accuracy of NSE in differentiating malignant pleural effusion (MPE) from benign pleural effusion (BPE) and investigate potential sources of heterogeneity in the diagnostic performance of NSE reported in previous studies.
Methods: We prospectively enrolled patients with undiagnosed pleural effusion from two centers in China (Hohhot and Changshu) and blindly measured their pleural fluid NSE level using an electrochemiluminescence assay. The diagnostic accuracy of NSE was assessed using a receiver operating characteristic (ROC) curve and decision curve analysis (DCA). We used the published studies to analyze the association between the prevalence of heart failure (HF) in the studied cohort and the diagnostic accuracy of NSE.
Results: The Hohhot center enrolled 153 patients (66 MPEs, 87 BPEs), and the Changshu center enrolled 58 patients (26 MPEs, 32 BPEs). MPE patients exhibited significantly higher levels of NSE compared to BPE patients in the Hohhot cohort. The areas under the curve (AUCs) for NSE were 0.68 [95% confidence interval (CI): 0.59-0.77] for the Hohhot cohort and 0.65 (95% CI: 0.51-0.79) for the Changshu cohort. The sensitivity and specificity of NSE in the Hohhot cohort were 0.50 (95% CI: 0.38-0.62) and 0.79 (95% CI: 0.70-0.86), respectively, at the 13.92 ng/mL threshold. In the Changshu cohort, the sensitivity and specificity of NSE were 0.42 (95% CI: 0.26-0.61) and 0.84 (95% CI: 0.68-0.93), respectively, at the 62.50 ng/mL threshold. The DCA of NSE was near the reference lines in both cohorts. HF prevalence was positively correlated with AUC in published studies.
Conclusions: The current evidence does not support that NSE serves as a useful diagnostic marker for MPE. The prevalence of HF patients in the studied cohort affects the diagnostic accuracy of NSE.
{"title":"Diagnostic value of pleural fluid neuron-specific enolase for malignant pleural effusion.","authors":"Xi Lin, Jian-Xun Wen, Yan Niu, Hong-Zhe Zhu, Cheng Yan, Su-Na Cha, Wen-Qi Zheng, Zhi-De Hu, Li Yan, Jin-Hong Huang, Hong Chen, Qianghua Zhou, Ting-Wang Jiang, Man Zhang","doi":"10.21037/jtd-2025-1538","DOIUrl":"10.21037/jtd-2025-1538","url":null,"abstract":"<p><strong>Background: </strong>Neuron-specific enolase (NSE) in pleural fluid has been proposed as a promising diagnostic biomarker. However, existing studies on the diagnostic accuracy of NSE have reported inconsistent results. This study aimed to assess the accuracy of NSE in differentiating malignant pleural effusion (MPE) from benign pleural effusion (BPE) and investigate potential sources of heterogeneity in the diagnostic performance of NSE reported in previous studies.</p><p><strong>Methods: </strong>We prospectively enrolled patients with undiagnosed pleural effusion from two centers in China (Hohhot and Changshu) and blindly measured their pleural fluid NSE level using an electrochemiluminescence assay. The diagnostic accuracy of NSE was assessed using a receiver operating characteristic (ROC) curve and decision curve analysis (DCA). We used the published studies to analyze the association between the prevalence of heart failure (HF) in the studied cohort and the diagnostic accuracy of NSE.</p><p><strong>Results: </strong>The Hohhot center enrolled 153 patients (66 MPEs, 87 BPEs), and the Changshu center enrolled 58 patients (26 MPEs, 32 BPEs). MPE patients exhibited significantly higher levels of NSE compared to BPE patients in the Hohhot cohort. The areas under the curve (AUCs) for NSE were 0.68 [95% confidence interval (CI): 0.59-0.77] for the Hohhot cohort and 0.65 (95% CI: 0.51-0.79) for the Changshu cohort. The sensitivity and specificity of NSE in the Hohhot cohort were 0.50 (95% CI: 0.38-0.62) and 0.79 (95% CI: 0.70-0.86), respectively, at the 13.92 ng/mL threshold. In the Changshu cohort, the sensitivity and specificity of NSE were 0.42 (95% CI: 0.26-0.61) and 0.84 (95% CI: 0.68-0.93), respectively, at the 62.50 ng/mL threshold. The DCA of NSE was near the reference lines in both cohorts. HF prevalence was positively correlated with AUC in published studies.</p><p><strong>Conclusions: </strong>The current evidence does not support that NSE serves as a useful diagnostic marker for MPE. The prevalence of HF patients in the studied cohort affects the diagnostic accuracy of NSE.</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"10969-10978"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780435/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31Epub Date: 2025-12-29DOI: 10.21037/jtd-2025-1330
Jinxiu He, De Jiang, Yifei Chen, Baotuan Wang, Yafeng Liu, Junjie Jia, Yiming Wang
Background: Airway epithelial cells (AECs) are crucial in respiratory tract. They are not only physical protective barriers, but also sensors of pathogens that release inflammatory mediators and chemokines that modulate the immune response. This study aims to explore global research trends on AECs-immune interactions via bibliometric analysis and provide immunology data to enhance understanding of AECs' role in respiratory disease immunity.
Methods: This study employed the Web of Science Core Collection (WOSCC) database to scan published data on AECs and immune responses from 2003 to 2023. The results were analyzed using bibliometric methods. Furthermore, statistical analysis was performed to assess the number of articles, publication years, distribution of author countries, and thematic areas.
Results: A total of 1,146 relevant articles were acquired. It was revealed that over the past two decades, there was a significant increase in studies focused on the relationship between AECs and immune responses. Moreover, most research topics comprised immune regulation of AECs, pathophysiology, and respiratory infections. Furthermore, most studies were from the United States, China, and European countries with universities and medical research centers being the most active research institutions.
Conclusions: Research on the association between AECs and immune responses is rapidly increasing globally and further investigation will increase the understanding of airway immune system regulation and the pathogenesis of respiratory diseases, thereby providing theoretical support for the development of novel therapeutic approaches and drug design.
背景:气道上皮细胞(AECs)在呼吸道中起着至关重要的作用。它们不仅是物理保护屏障,也是病原体的传感器,释放炎症介质和调节免疫反应的趋化因子。本研究旨在通过文献计量学分析,探索aec -免疫相互作用的全球研究趋势,并提供免疫学数据,以提高对aec在呼吸系统疾病免疫中的作用的认识。方法:本研究采用Web of Science Core Collection (WOSCC)数据库扫描2003 - 2023年已发表的AECs和免疫应答数据。采用文献计量学方法对结果进行分析。此外,还进行了统计分析,以评估文章数量、出版年份、作者国家分布和专题领域。结果:共获得相关文献1146篇。据透露,在过去二十年中,关注aec与免疫反应之间关系的研究显著增加。此外,大多数研究课题包括AECs的免疫调节、病理生理学和呼吸道感染。此外,大多数研究来自美国、中国和欧洲国家,其中大学和医学研究中心是最活跃的研究机构。结论:在全球范围内,对AECs与免疫应答之间关系的研究正在迅速增加,进一步的研究将增加对气道免疫系统调节和呼吸系统疾病发病机制的认识,从而为开发新的治疗方法和药物设计提供理论支持。
{"title":"Global research trends in airway epithelial cell immune responses: a bibliometric study.","authors":"Jinxiu He, De Jiang, Yifei Chen, Baotuan Wang, Yafeng Liu, Junjie Jia, Yiming Wang","doi":"10.21037/jtd-2025-1330","DOIUrl":"10.21037/jtd-2025-1330","url":null,"abstract":"<p><strong>Background: </strong>Airway epithelial cells (AECs) are crucial in respiratory tract. They are not only physical protective barriers, but also sensors of pathogens that release inflammatory mediators and chemokines that modulate the immune response. This study aims to explore global research trends on AECs-immune interactions via bibliometric analysis and provide immunology data to enhance understanding of AECs' role in respiratory disease immunity.</p><p><strong>Methods: </strong>This study employed the Web of Science Core Collection (WOSCC) database to scan published data on AECs and immune responses from 2003 to 2023. The results were analyzed using bibliometric methods. Furthermore, statistical analysis was performed to assess the number of articles, publication years, distribution of author countries, and thematic areas.</p><p><strong>Results: </strong>A total of 1,146 relevant articles were acquired. It was revealed that over the past two decades, there was a significant increase in studies focused on the relationship between AECs and immune responses. Moreover, most research topics comprised immune regulation of AECs, pathophysiology, and respiratory infections. Furthermore, most studies were from the United States, China, and European countries with universities and medical research centers being the most active research institutions.</p><p><strong>Conclusions: </strong>Research on the association between AECs and immune responses is rapidly increasing globally and further investigation will increase the understanding of airway immune system regulation and the pathogenesis of respiratory diseases, thereby providing theoretical support for the development of novel therapeutic approaches and drug design.</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"10758-10770"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780432/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This article provides a systematic analysis and commentary on the North American Expert Consensus regarding the clinical role of ex vivo lung perfusion (EVLP) using acellular perfusate. The consensus outlines key recommendations, including general statements on EVLP, criteria for donor lung selection, critical assessment parameters during perfusion, and a decision-making framework for transplantation. It emphasizes that current clinical practice relies heavily on small-scale, non-randomized, single-center studies, which often require substantial reliance on clinical judgment and institutional experience. As a result, the consensus calls for further, more rigorous research to establish evidence-based guidelines for EVLP-related decisions. By integrating the consensus recommendations with recent advancements in both basic and clinical EVLP research, this article examines the clinical relevance of various decision-making criteria and evaluation frameworks. It also explores EVLP management strategies within specific clinical contexts identified in the consensus. Additionally, the article discusses the inherent logistical and economic challenges associated with implementing EVLP in clinical settings. By clarifying both established principles and ongoing controversies, this review aims to bridge the gap between theoretical consensus and clinical practice, and to provide a useful reference for standardizing EVLP protocols, improving donor lung quality, expanding the donor pool, and enhancing transplant outcomes.
{"title":"An interpretative review of North American expert consensus on the clinical role of ex vivo lung perfusion (EVLP) with acellular perfusate.","authors":"Wei-Yang Chen, Zhi-Qiang Deng, Hao-Ji Yan, Xiang-Yun Zheng, Zeng-Wei Yu, Xiao-Han Jin, Xin-Yue Zhang, Ze-Hui Liu, Ya-Ling Liu, Jia-Sheng Zhao, Shi-Xiang Liu, Bo-Yang Xia, Yang Zhao, Yang Li, Xian He, Wen-Ya Li, Masaaki Sato, Dong Tian","doi":"10.21037/jtd-2025-1599","DOIUrl":"10.21037/jtd-2025-1599","url":null,"abstract":"<p><p>This article provides a systematic analysis and commentary on the North American Expert Consensus regarding the clinical role of ex vivo lung perfusion (EVLP) using acellular perfusate. The consensus outlines key recommendations, including general statements on EVLP, criteria for donor lung selection, critical assessment parameters during perfusion, and a decision-making framework for transplantation. It emphasizes that current clinical practice relies heavily on small-scale, non-randomized, single-center studies, which often require substantial reliance on clinical judgment and institutional experience. As a result, the consensus calls for further, more rigorous research to establish evidence-based guidelines for EVLP-related decisions. By integrating the consensus recommendations with recent advancements in both basic and clinical EVLP research, this article examines the clinical relevance of various decision-making criteria and evaluation frameworks. It also explores EVLP management strategies within specific clinical contexts identified in the consensus. Additionally, the article discusses the inherent logistical and economic challenges associated with implementing EVLP in clinical settings. By clarifying both established principles and ongoing controversies, this review aims to bridge the gap between theoretical consensus and clinical practice, and to provide a useful reference for standardizing EVLP protocols, improving donor lung quality, expanding the donor pool, and enhancing transplant outcomes.</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"11377-11388"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780431/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31Epub Date: 2025-12-29DOI: 10.21037/jtd-2025-693
Jiahui Jin, Yuxing Chen, Qingpeng Zeng, Muyu Li, Jun Zhao
<p><strong>Background: </strong>Tracheal, bronchus, and lung (TBL) cancer remains a major global health burden, particularly among adults aged ≥55 years. Despite medical advancements, rising incidence in middle-aged adults and persistent regional disparities underscore the need for targeted public health strategies. Comprehensive analysis integrating global burden, socio-demographic factors, and future projections is essential to guide public health interventions and resource allocation. This study aims to assess the global, regional, and national patterns of TBL cancer burden, identify the impact of socio-demographic factors, and project future trends to inform effective prevention and control strategies.</p><p><strong>Methods: </strong>Using Global Burden of Disease (GBD) 2021 data, we analyzed TBL cancer incidence, mortality, and disability-adjusted life years (DALYs) across 204 countries from 1990 to 2021. Data were sourced from national cancer registries, health surveys, and statistical estimates. Temporal trends were assessed using join-point regression to identify significant inflection points in disease burden. Healthcare system efficiency was evaluated with data envelopment analysis (DEA) and stochastic frontier analysis (SFA). Projections for 2036 were made using an autoregressive integrated moving average (ARIMA) model, incorporating historical trends and population data obtained from GBD.</p><p><strong>Results: </strong>In 2021, TBL cancers resulted in 2.02 million new cases, 1.81 million deaths, and 37.63 million DALYs globally among adults aged ≥55 years. East Asia bore the highest burden, while Sub-Saharan Africa had the lowest. Men had significantly higher incidence and mortality than women, with DALY rates peaking in high-middle Socio-Demographic Index (SDI) regions. High-income nations exhibited declining trends, whereas low-middle SDI countries showed rising burdens, particularly among males. Join-point regression analysis results revealed that incidence rates declined in more than half of the countries, including Australia [average annual percentage change (AAPC), -0.56] and Canada (AAPC, -0.81), with the most pronounced reductions in Greenland (AAPC, -1.25) and Kazakhstan (AAPC, -2.46). In contrast, Egypt exhibited the highest growth (AAPC, +3.45). The ARIMA model projected continued decline in mortality in high-SDI regions, stabilization in middle-SDI regions, and persistent or increasing burden in low-SDI countries, especially for males.</p><p><strong>Conclusions: </strong>The global TBL cancer burden reflects a complex interplay of socioeconomic development, tobacco control, and environmental risk factors. Forecasts suggest widening disparities, with lower SDI regions expected to face a continued rise in mortality. Addressing gender disparities, expanding genomic and early detection programs in high-burden regions, and implementing scalable environmental policies in resource-limited settings are critical for improving outc
{"title":"Global, regional and national burden of trachea, bronchus, and lung cancer in middle-aged and elderly people aged 55+ years from 1990 to 2021, with projections to 2036: a systematic analysis of the Global Burden of Disease Study 2021.","authors":"Jiahui Jin, Yuxing Chen, Qingpeng Zeng, Muyu Li, Jun Zhao","doi":"10.21037/jtd-2025-693","DOIUrl":"10.21037/jtd-2025-693","url":null,"abstract":"<p><strong>Background: </strong>Tracheal, bronchus, and lung (TBL) cancer remains a major global health burden, particularly among adults aged ≥55 years. Despite medical advancements, rising incidence in middle-aged adults and persistent regional disparities underscore the need for targeted public health strategies. Comprehensive analysis integrating global burden, socio-demographic factors, and future projections is essential to guide public health interventions and resource allocation. This study aims to assess the global, regional, and national patterns of TBL cancer burden, identify the impact of socio-demographic factors, and project future trends to inform effective prevention and control strategies.</p><p><strong>Methods: </strong>Using Global Burden of Disease (GBD) 2021 data, we analyzed TBL cancer incidence, mortality, and disability-adjusted life years (DALYs) across 204 countries from 1990 to 2021. Data were sourced from national cancer registries, health surveys, and statistical estimates. Temporal trends were assessed using join-point regression to identify significant inflection points in disease burden. Healthcare system efficiency was evaluated with data envelopment analysis (DEA) and stochastic frontier analysis (SFA). Projections for 2036 were made using an autoregressive integrated moving average (ARIMA) model, incorporating historical trends and population data obtained from GBD.</p><p><strong>Results: </strong>In 2021, TBL cancers resulted in 2.02 million new cases, 1.81 million deaths, and 37.63 million DALYs globally among adults aged ≥55 years. East Asia bore the highest burden, while Sub-Saharan Africa had the lowest. Men had significantly higher incidence and mortality than women, with DALY rates peaking in high-middle Socio-Demographic Index (SDI) regions. High-income nations exhibited declining trends, whereas low-middle SDI countries showed rising burdens, particularly among males. Join-point regression analysis results revealed that incidence rates declined in more than half of the countries, including Australia [average annual percentage change (AAPC), -0.56] and Canada (AAPC, -0.81), with the most pronounced reductions in Greenland (AAPC, -1.25) and Kazakhstan (AAPC, -2.46). In contrast, Egypt exhibited the highest growth (AAPC, +3.45). The ARIMA model projected continued decline in mortality in high-SDI regions, stabilization in middle-SDI regions, and persistent or increasing burden in low-SDI countries, especially for males.</p><p><strong>Conclusions: </strong>The global TBL cancer burden reflects a complex interplay of socioeconomic development, tobacco control, and environmental risk factors. Forecasts suggest widening disparities, with lower SDI regions expected to face a continued rise in mortality. Addressing gender disparities, expanding genomic and early detection programs in high-burden regions, and implementing scalable environmental policies in resource-limited settings are critical for improving outc","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"11039-11056"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780452/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952328","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31Epub Date: 2025-12-29DOI: 10.21037/jtd-2025-1858
Heng Tao, Sida Lu, Xuanyu Zhu, Zhuangzhuang Cong, Jing Luo, Haifeng Du, Chenxu Liu, Haiwei Wu, Yi Shen
Background: The benefit of adjuvant chemotherapy (ACT) in stage IB non-small cell lung cancer (NSCLC) remains controversial, particularly for patients with high-risk features [visceral pleural invasion (VPI), lymphovascular invasion (LVI), poor differentiation]. This study aimed to evaluate the efficacy of ACT in this cohort.
Methods: We retrospectively analyzed 356 patients with stage IB [American Joint Committee on Cancer (AJCC) 9th edition] lung adenocarcinoma treated from 2016 to 2019, of whom 276 with at least one high-risk factor were included in the study. Propensity score matching (PSM) was used to balance baseline characteristics (n=106 per group). Disease-free survival (DFS) and overall survival (OS) were compared between the ACT and non-ACT groups.
Results: ACT significantly improved DFS [hazard ratio (HR) =0.471, P=0.001] and OS (HR =0.519, P=0.03). Subgroup analysis revealed that the benefit was grade-dependent: patients with poorly differentiated (G3) tumors had a 66.5% lower risk of recurrence with ACT (HR =0.335, P=0.001), while those with moderately differentiated (G2) tumors derived no significant benefit (HR =1.041, P=0.91). High-grade histologic patterns (solid, micropapillary, and complex glandular), LVI, and tumor size were independent predictors of poor survival. VPI status did not significantly influence ACT efficacy (P=0.95).
Conclusions: ACT provides survival benefits for stage IB NSCLC patients with high-risk features, especially in poorly differentiated (G3) tumors. Histologic grading might serve as a useful tool to guide ACT decisions and to avoid potential overtreatment in moderately differentiated (G2) subgroups.
{"title":"Grade-driven adjuvant chemotherapy benefit in high-risk stage IB NSCLC: a retrospective cohort study.","authors":"Heng Tao, Sida Lu, Xuanyu Zhu, Zhuangzhuang Cong, Jing Luo, Haifeng Du, Chenxu Liu, Haiwei Wu, Yi Shen","doi":"10.21037/jtd-2025-1858","DOIUrl":"10.21037/jtd-2025-1858","url":null,"abstract":"<p><strong>Background: </strong>The benefit of adjuvant chemotherapy (ACT) in stage IB non-small cell lung cancer (NSCLC) remains controversial, particularly for patients with high-risk features [visceral pleural invasion (VPI), lymphovascular invasion (LVI), poor differentiation]. This study aimed to evaluate the efficacy of ACT in this cohort.</p><p><strong>Methods: </strong>We retrospectively analyzed 356 patients with stage IB [American Joint Committee on Cancer (AJCC) 9th edition] lung adenocarcinoma treated from 2016 to 2019, of whom 276 with at least one high-risk factor were included in the study. Propensity score matching (PSM) was used to balance baseline characteristics (n=106 per group). Disease-free survival (DFS) and overall survival (OS) were compared between the ACT and non-ACT groups.</p><p><strong>Results: </strong>ACT significantly improved DFS [hazard ratio (HR) =0.471, P=0.001] and OS (HR =0.519, P=0.03). Subgroup analysis revealed that the benefit was grade-dependent: patients with poorly differentiated (G3) tumors had a 66.5% lower risk of recurrence with ACT (HR =0.335, P=0.001), while those with moderately differentiated (G2) tumors derived no significant benefit (HR =1.041, P=0.91). High-grade histologic patterns (solid, micropapillary, and complex glandular), LVI, and tumor size were independent predictors of poor survival. VPI status did not significantly influence ACT efficacy (P=0.95).</p><p><strong>Conclusions: </strong>ACT provides survival benefits for stage IB NSCLC patients with high-risk features, especially in poorly differentiated (G3) tumors. Histologic grading might serve as a useful tool to guide ACT decisions and to avoid potential overtreatment in moderately differentiated (G2) subgroups.</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"11262-11273"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780445/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: The validity and safety of simultaneously performing coronary artery bypass grafting (CABG) and lung cancer resection remain inconclusive. This study examined the clinical progression of patients undergone this surgery.
Methods: Fifty-seven patients who underwent concurrent off-pump CABG (OPCABG) and pulmonary lobectomy between May 2006 and December 2019 in Beijing Anzhen Hospital were retrospectively analyzed. Baseline characteristic and clinical data of patients were collected, and postoperative follow-up was performed to evaluate the prognosis.
Results: All procedures were performed with median or parasternal incision, and thoracoscope was used in 15 of them. No intraoperative deaths were reported. An average of 2.52±0.90 coronary vessels were grafted per procedure. One patient died in hospital due to postoperative low cardiac output, another due to respiratory failure. In Cox multivariate regression analysis, age >69 years [hazard ratio (HR): 1.223, 95% confidence interval (CI): 1.067-1.402, P=0.004, area under the curve (AUC) =0.657] and tumor stage >III (HR: 5.384, 95% CI: 1.917-15.125, P=0.001, AUC =0.715) emerged as significant predictors of adverse event risk for survival. During the 17-year follow-up, the mean survival time was 85.39±49.70 months, with a primary endpoint of death reached by 21.05% (12/57) of patients. All deaths were attributed to tumor progression, and there were no new myocardial infarction or heart failure readmissions.
Conclusions: OPCABG combined with pulmonary resection is safe and effective in the treatment of patients with concomitant coronary artery disease (CAD) and lung cancer. Age and tumor stage were significantly correlated with postoperative survival. The predictive value of tumor stage above III surpasses that of age in prognostic assessment. For patients aged 69 years and with tumors of stage III or higher, surgical decision-making requires careful consideration due to the potentially increased risk of adverse outcomes.
{"title":"Long-term survival of patients undergoing off-pump coronary artery bypass grafting combined with pulmonary lobectomy.","authors":"Shifeng Zhao, Muhua Zhao, Hao Cui, Shengwei Wang, Changwei Ren, Fangjiong Huang, Xuchen Ma, Songlei Ou, Yongqiang Lai, Hongchang Guo","doi":"10.21037/jtd-2025-695","DOIUrl":"10.21037/jtd-2025-695","url":null,"abstract":"<p><strong>Background: </strong>The validity and safety of simultaneously performing coronary artery bypass grafting (CABG) and lung cancer resection remain inconclusive. This study examined the clinical progression of patients undergone this surgery.</p><p><strong>Methods: </strong>Fifty-seven patients who underwent concurrent off-pump CABG (OPCABG) and pulmonary lobectomy between May 2006 and December 2019 in Beijing Anzhen Hospital were retrospectively analyzed. Baseline characteristic and clinical data of patients were collected, and postoperative follow-up was performed to evaluate the prognosis.</p><p><strong>Results: </strong>All procedures were performed with median or parasternal incision, and thoracoscope was used in 15 of them. No intraoperative deaths were reported. An average of 2.52±0.90 coronary vessels were grafted per procedure. One patient died in hospital due to postoperative low cardiac output, another due to respiratory failure. In Cox multivariate regression analysis, age >69 years [hazard ratio (HR): 1.223, 95% confidence interval (CI): 1.067-1.402, P=0.004, area under the curve (AUC) =0.657] and tumor stage >III (HR: 5.384, 95% CI: 1.917-15.125, P=0.001, AUC =0.715) emerged as significant predictors of adverse event risk for survival. During the 17-year follow-up, the mean survival time was 85.39±49.70 months, with a primary endpoint of death reached by 21.05% (12/57) of patients. All deaths were attributed to tumor progression, and there were no new myocardial infarction or heart failure readmissions.</p><p><strong>Conclusions: </strong>OPCABG combined with pulmonary resection is safe and effective in the treatment of patients with concomitant coronary artery disease (CAD) and lung cancer. Age and tumor stage were significantly correlated with postoperative survival. The predictive value of tumor stage above III surpasses that of age in prognostic assessment. For patients aged 69 years and with tumors of stage III or higher, surgical decision-making requires careful consideration due to the potentially increased risk of adverse outcomes.</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"11090-11099"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780460/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31Epub Date: 2025-12-29DOI: 10.21037/jtd-2025-250
Luyu Yang, Zhimin Cao, Yuanfang Xing, Yuanming Pan, Can Yang, Li Zhang, Hong Zhao, Teng Ma, Huan Ye
<p><strong>Background: </strong>Acute respiratory distress syndrome (ARDS) is a complex syndrome characterized by acute diffuse lung injury and progressive respiratory failure, caused by various intra- and extra-pulmonary factors. The coronavirus disease 2019 (COVID-19) pandemic has significantly increased the incidence of ARDS, posing a tremendous threat to human health due to its high mortality rate and lack of effective therapeutic drugs. In recent years, mesenchymal stem cell-derived exosomes (MSC-exo) have been considered a new hope for the treatment of ARDS due to their potent immunomodulatory characteristics. Although multiple studies have demonstrated their efficacy and safety, the differential therapeutic effects of various administration routes and doses remain unclear. This study aimed to investigate the administration route of MSC-exo for ARDS treatment, with the goal of maximizing therapeutic benefits and providing valuable clinical insights.</p><p><strong>Methods: </strong>This study aims to establish an ARDS disease model by intratracheal instillation of lipopolysaccharide (LPS) in male C57/BL6 mice. Subsequently, umbilical cord mesenchymal stem cell exosomes will be administered via three methods: inhalation, tail vein injection, and combination therapy (inhalation combined with tail vein injection). Following the establishment of the mouse ARDS model via intratracheal instillation of LPS, the animals were randomly divided into seven groups based on the timing and dosage of the treatment administration. Samples were harvested at 24 hours, 72 hours, and 7 days after modeling. The assessments included RNA transcriptome sequencing, cytokine levels in blood and bronchoalveolar lavage fluid, blood oxygen saturation, histopathological staining, and survival analysis.</p><p><strong>Results: </strong>Compared to nebulized exosomes alone, dual-route administration significantly improved respiratory function, as evidenced by prolonged expiratory and inspiratory times and increased minute ventilation (P≤0.05). Furthermore, it decreased the levels of the pro-inflammatory cytokines interleukin-1β (IL-1β) and interleukin-6 (IL-6) in the blood (P=0.01, P=0.041). Compared to intravenous exosomes alone, dual-route administration produced broader improvements. It significantly enhanced lung function by prolonging expiratory time (P=0.01), inspiratory time (P=0.004), and increasing minute ventilation (P=0.02). Additionally, it suppressed inflammation by lowering IL-6 levels in bronchoalveolar lavage fluid (P=0.01) and reduced the death of type II alveolar epithelial cells (P=0.03).</p><p><strong>Conclusions: </strong>The dual-route administration of umbilical cord MSC-exo is more effective in controlling the inflammatory response and alleviating lung injury in LPS-induced ARDS animal models. Inhalation rapidly alleviates pulmonary inflammation with a smaller dose, while intravenous injection better manages the systemic inflammation. This dual-route
{"title":"Inhalation & intravenous: umbilical cord mesenchymal stem cell-derived exosomes therapy strategy for acute respiratory distress syndrome in a murine model.","authors":"Luyu Yang, Zhimin Cao, Yuanfang Xing, Yuanming Pan, Can Yang, Li Zhang, Hong Zhao, Teng Ma, Huan Ye","doi":"10.21037/jtd-2025-250","DOIUrl":"10.21037/jtd-2025-250","url":null,"abstract":"<p><strong>Background: </strong>Acute respiratory distress syndrome (ARDS) is a complex syndrome characterized by acute diffuse lung injury and progressive respiratory failure, caused by various intra- and extra-pulmonary factors. The coronavirus disease 2019 (COVID-19) pandemic has significantly increased the incidence of ARDS, posing a tremendous threat to human health due to its high mortality rate and lack of effective therapeutic drugs. In recent years, mesenchymal stem cell-derived exosomes (MSC-exo) have been considered a new hope for the treatment of ARDS due to their potent immunomodulatory characteristics. Although multiple studies have demonstrated their efficacy and safety, the differential therapeutic effects of various administration routes and doses remain unclear. This study aimed to investigate the administration route of MSC-exo for ARDS treatment, with the goal of maximizing therapeutic benefits and providing valuable clinical insights.</p><p><strong>Methods: </strong>This study aims to establish an ARDS disease model by intratracheal instillation of lipopolysaccharide (LPS) in male C57/BL6 mice. Subsequently, umbilical cord mesenchymal stem cell exosomes will be administered via three methods: inhalation, tail vein injection, and combination therapy (inhalation combined with tail vein injection). Following the establishment of the mouse ARDS model via intratracheal instillation of LPS, the animals were randomly divided into seven groups based on the timing and dosage of the treatment administration. Samples were harvested at 24 hours, 72 hours, and 7 days after modeling. The assessments included RNA transcriptome sequencing, cytokine levels in blood and bronchoalveolar lavage fluid, blood oxygen saturation, histopathological staining, and survival analysis.</p><p><strong>Results: </strong>Compared to nebulized exosomes alone, dual-route administration significantly improved respiratory function, as evidenced by prolonged expiratory and inspiratory times and increased minute ventilation (P≤0.05). Furthermore, it decreased the levels of the pro-inflammatory cytokines interleukin-1β (IL-1β) and interleukin-6 (IL-6) in the blood (P=0.01, P=0.041). Compared to intravenous exosomes alone, dual-route administration produced broader improvements. It significantly enhanced lung function by prolonging expiratory time (P=0.01), inspiratory time (P=0.004), and increasing minute ventilation (P=0.02). Additionally, it suppressed inflammation by lowering IL-6 levels in bronchoalveolar lavage fluid (P=0.01) and reduced the death of type II alveolar epithelial cells (P=0.03).</p><p><strong>Conclusions: </strong>The dual-route administration of umbilical cord MSC-exo is more effective in controlling the inflammatory response and alleviating lung injury in LPS-induced ARDS animal models. Inhalation rapidly alleviates pulmonary inflammation with a smaller dose, while intravenous injection better manages the systemic inflammation. This dual-route ","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"11100-11117"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780377/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952460","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: There is no consensus on whether a thorough mediastinal lymph node dissection (MLND) is necessary for stage I lung adenocarcinoma (AD) patients who require lobectomy. This study aimed to evaluate the survival impact of MLND in patients with T1 stage lung AD undergoing lobectomy.
Methods: We conducted a retrospective cohort study of 5,398 patients diagnosed with lung AD (tumor diameter 1-29 mm) from 2004 to 2015, utilizing data from the Surveillance, Epidemiology, and End Results (SEER) program. Patients were treated with either lobectomy only or lobectomy with MLND. The primary endpoint was overall survival (OS), analyzed using Kaplan-Meier survival analysis, Chi-squared testing, and Cox regression analysis.
Results: At a median follow-up of 97 months, the median survival duration for patients with T1a lung AD who underwent lobectomy with MLND was significantly longer (143 months), compared to those who underwent lobectomy alone (79 months, P<0.001). Similar survival benefits were found for T1b and T1c lung AD. Multivariate analysis revealed that lobectomy with MLND was an independent prognostic factor for patients with T1 stage lung AD [hazard ratio (HR) =0.731; 95% confidence interval (CI): 0.639-0.837; P<0.001]. Other significant prognostic factors included gender, age, N stage, and treatment modalities.
Conclusions: Our findings suggest that MLND significantly improves survival in patients with T1 stage lung AD, highlighting its importance as a surgical strategy. Further prospective randomized controlled trials are needed to confirm these findings.
{"title":"Mediastinal lymph node dissection in T1 stage lung adenocarcinoma: a retrospective analysis of survival outcomes and prognostic factors from the SEER database.","authors":"Bingqun Wu, Xiying Cao, Yong Cui, Shenhai Wei, Shouqiang Pan, Pengcheng Hu, Hui Li","doi":"10.21037/jtd-2025-1743","DOIUrl":"10.21037/jtd-2025-1743","url":null,"abstract":"<p><strong>Background: </strong>There is no consensus on whether a thorough mediastinal lymph node dissection (MLND) is necessary for stage I lung adenocarcinoma (AD) patients who require lobectomy. This study aimed to evaluate the survival impact of MLND in patients with T1 stage lung AD undergoing lobectomy.</p><p><strong>Methods: </strong>We conducted a retrospective cohort study of 5,398 patients diagnosed with lung AD (tumor diameter 1-29 mm) from 2004 to 2015, utilizing data from the Surveillance, Epidemiology, and End Results (SEER) program. Patients were treated with either lobectomy only or lobectomy with MLND. The primary endpoint was overall survival (OS), analyzed using Kaplan-Meier survival analysis, Chi-squared testing, and Cox regression analysis.</p><p><strong>Results: </strong>At a median follow-up of 97 months, the median survival duration for patients with T1a lung AD who underwent lobectomy with MLND was significantly longer (143 months), compared to those who underwent lobectomy alone (79 months, P<0.001). Similar survival benefits were found for T1b and T1c lung AD. Multivariate analysis revealed that lobectomy with MLND was an independent prognostic factor for patients with T1 stage lung AD [hazard ratio (HR) =0.731; 95% confidence interval (CI): 0.639-0.837; P<0.001]. Other significant prognostic factors included gender, age, N stage, and treatment modalities.</p><p><strong>Conclusions: </strong>Our findings suggest that MLND significantly improves survival in patients with T1 stage lung AD, highlighting its importance as a surgical strategy. Further prospective randomized controlled trials are needed to confirm these findings.</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"11161-11171"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780382/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952468","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31Epub Date: 2025-12-29DOI: 10.21037/jtd-2025b-14
[This corrects the article DOI: 10.21037/jtd-23-1975.].
[这更正了文章DOI: 10.21037/jtd-23-1975]。
{"title":"Erratum: Promotion of non-small cell lung cancer tumor growth by <i>FHL2</i> via inducing angiogenesis and vascular permeability.","authors":"","doi":"10.21037/jtd-2025b-14","DOIUrl":"10.21037/jtd-2025b-14","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.21037/jtd-23-1975.].</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"11526-11530"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780453/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952539","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31Epub Date: 2025-12-29DOI: 10.21037/jtd-2025-1320
Yefeng Chen, Weiqiang Mo, Yanmin Pei, Haiqin Wang
Background: Lung squamous cell carcinoma (LSCC) is a prevalent subtype of non-small cell lung cancer (NSCLC). While there have been some prognostic models for LSCC, models specifically addressing stage IIIA LSCC are still limited. The aim of this study is to develop a nomogram to predict the overall survival (OS) of patients with stage IIIA LSCC.
Methods: Patients diagnosed with LSCC between 2,010 and 2,015 were collected from the Surveillance, Epidemiology, and End Results (SEER) database, and their basic clinical characteristics were analyzed. A 1:1 propensity score matching (PSM) analysis was performed to balance the baseline characteristics of the patients. The OS of patients was evaluated using Kaplan-Meier analysis and compared with the log-rank test. Clinical prognostic factors related to OS were analyzed using univariate and multivariate Cox regressions, and a visual nomogram model for predicting patient prognosis was developed and validated.
Results: This study included 4,268 patients with stage IIIA LSCC, comprising 1,157 cases in the cancer-directed surgery (CDS) group and 3,111 cases in the no-cancer-directed surgery (no-CDS) group. After PSM, 1,095 patients in the CDS group were matched with 1,095 patients in the no-CDS group. Kaplan-Meier survival analysis revealed the significant beneficial effect of surgery on OS in both the original and matched cohorts. Multivariate Cox analysis indicated that sex, age, marital status, surgery, and chemotherapy were independent prognostic factors for stage IIIA LSCC. Additionally, the receiver operating characteristic (ROC) curve, calibration curve, and decision curve analysis (DCA) curve demonstrated strong predictive performance in both the training and validation cohorts of the prognostic nomogram.
Conclusions: Through univariate and multivariate Cox regression analyses, sex, age, marital status, surgery, and chemotherapy were identified as independent prognostic risk factors for OS in patients with stage IIIA LSCC. A nomogram was successfully developed to assist clinicians in making more informed treatment decisions.
{"title":"Prognosis of surgery and nomogram for patients with IIIA lung squamous cell carcinoma: a propensity score matched SEER database analysis.","authors":"Yefeng Chen, Weiqiang Mo, Yanmin Pei, Haiqin Wang","doi":"10.21037/jtd-2025-1320","DOIUrl":"10.21037/jtd-2025-1320","url":null,"abstract":"<p><strong>Background: </strong>Lung squamous cell carcinoma (LSCC) is a prevalent subtype of non-small cell lung cancer (NSCLC). While there have been some prognostic models for LSCC, models specifically addressing stage IIIA LSCC are still limited. The aim of this study is to develop a nomogram to predict the overall survival (OS) of patients with stage IIIA LSCC.</p><p><strong>Methods: </strong>Patients diagnosed with LSCC between 2,010 and 2,015 were collected from the Surveillance, Epidemiology, and End Results (SEER) database, and their basic clinical characteristics were analyzed. A 1:1 propensity score matching (PSM) analysis was performed to balance the baseline characteristics of the patients. The OS of patients was evaluated using Kaplan-Meier analysis and compared with the log-rank test. Clinical prognostic factors related to OS were analyzed using univariate and multivariate Cox regressions, and a visual nomogram model for predicting patient prognosis was developed and validated.</p><p><strong>Results: </strong>This study included 4,268 patients with stage IIIA LSCC, comprising 1,157 cases in the cancer-directed surgery (CDS) group and 3,111 cases in the no-cancer-directed surgery (no-CDS) group. After PSM, 1,095 patients in the CDS group were matched with 1,095 patients in the no-CDS group. Kaplan-Meier survival analysis revealed the significant beneficial effect of surgery on OS in both the original and matched cohorts. Multivariate Cox analysis indicated that sex, age, marital status, surgery, and chemotherapy were independent prognostic factors for stage IIIA LSCC. Additionally, the receiver operating characteristic (ROC) curve, calibration curve, and decision curve analysis (DCA) curve demonstrated strong predictive performance in both the training and validation cohorts of the prognostic nomogram.</p><p><strong>Conclusions: </strong>Through univariate and multivariate Cox regression analyses, sex, age, marital status, surgery, and chemotherapy were identified as independent prognostic risk factors for OS in patients with stage IIIA LSCC. A nomogram was successfully developed to assist clinicians in making more informed treatment decisions.</p>","PeriodicalId":17542,"journal":{"name":"Journal of thoracic disease","volume":"17 12","pages":"10670-10682"},"PeriodicalIF":1.9,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780403/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952552","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}