The prognosis and treatment consideration for non-small cell lung carcinoma patients with tumor size of >2.0-3.0 cm and visceral pleural invasion: a SEER-based study.

IF 1.5 4区 医学 Q4 ONCOLOGY
Translational cancer research Pub Date : 2024-11-30 Epub Date: 2024-11-27 DOI:10.21037/tcr-24-33
Xirui Lin, Haijie Xu, Jianrong Chen, Jiaying Wu, Jiong Lin, Hansheng Wu
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引用次数: 0

Abstract

Background: Lung cancer is the most prevailing oncological disease worldwide. Visceral pleural invasion (VPI) has been proven to be a poor prognosis factor for early-stage non-small cell lung carcinoma (NSCLC) patients. However, there remains some debate regarding whether NSCLC patients with tumor size (TS) ranging from >2.0 to 3.0 cm and VPI should be considered for postoperative treatment. This study compared the prognosis of T2a and T2b NSCLC patients, specifically focusing on those with VPI and TS ranging from >2.0-3.0 cm to emphasize the severity of the disease. Additionally, the impact of adjuvant therapies on the outcome of these patients was discussed.

Methods: This retrospective research utilized data from the Surveillance, Epidemiology, and End Results (SEER) database, which provided a comprehensive dataset of 10,452 patients diagnosed with pN0M0 NSCLC with TS intervals of >2.0-5.0 cm between 2010 and 2019. The SEER database, renowned for its expansive and population-based cancer data, provides a robust platform for researchers to access a large cohort of patients diagnosed with NSCLC. Survival probabilities were calculated by the Kaplan-Meier method and compared between groups with Log-rank test. Univariate and multivariate logistic analyses were used to identify independent risk factors of VPI.

Results: Patients with NSCLC and TS between >2.0 and 3.0 cm, along with VPI, had a worse 5-year overall survival rate compared to those at T2a stage (49.1% vs. 56.8%, P=0.03) and T2b stage (45.4% vs. 64.2%, P<0.0001). However, no statistical significance was observed when comparing patients with TS range between >2.0 and 3.0 cm and presenting with VPI to those staged T2b and received adjuvant chemotherapy (48.4% vs. 48.5%, P=0.54). Patients with clinical stage of T1c and VPI positive had significantly better prognosis after receiving chemotherapy (34.5% vs. 55.2%, P<0.001). Logistic analysis indicated that age older than 65 years old, poor differentiated and undifferentiated, as well as sub-lobectomy resection were independent risk factors for VPI in NSCLC.

Conclusions: Postoperative chemotherapy can improve the prognosis of patients with TS ranging from >2.0 to 3.0 cm with VPI. According to the analysis of OS based on the postoperative chemotherapy, patients with NSCLC featuring TS extend from >2.0 to 3.0 cm and VPI may be classified within stage IIA. Consequently, the consideration of postoperative chemotherapy for this patient cohort may be warranted.

肿瘤大小为>2.0 ~ 3.0 cm并内脏性胸膜侵犯的非小细胞肺癌患者的预后及治疗考虑:基于seer的研究。
背景:肺癌是世界上最常见的肿瘤疾病。内脏胸膜侵犯(VPI)已被证明是早期非小细胞肺癌(NSCLC)患者预后不良的因素。然而,对于肿瘤大小(TS)介于>2.0 ~ 3.0 cm和VPI的NSCLC患者是否应该考虑术后治疗,仍存在一些争论。本研究比较了T2a和T2b NSCLC患者的预后,特别关注VPI和TS在>2.0-3.0 cm之间的患者,以强调疾病的严重程度。此外,还讨论了辅助治疗对这些患者预后的影响。方法:本回顾性研究利用来自监测、流行病学和最终结果(SEER)数据库的数据,该数据库提供了2010年至2019年期间10,452例诊断为pN0M0 NSCLC的患者的综合数据集,TS间隔为>2.0-5.0 cm。SEER数据库以其广泛和基于人群的癌症数据而闻名,为研究人员提供了一个强大的平台,可以访问大量被诊断为非小细胞肺癌的患者。生存率采用Kaplan-Meier法计算,组间比较采用Log-rank检验。采用单因素和多因素logistic分析确定VPI的独立危险因素。结果:与T2a期(49.1% vs. 56.8%, P=0.03)和T2b期(45.4% vs. 64.2%, P2.0和3.0 cm)相比,伴有VPI的NSCLC和TS患者的5年总生存率(48.4% vs. 48.5%, P=0.54)较差。临床分期T1c和VPI阳性患者接受化疗后预后明显较好(34.5% vs. 55.2%)。结论:术后化疗可改善>2.0 ~ 3.0 cm伴有VPI的TS患者预后。根据术后化疗的OS分析,伴有TS的NSCLC患者从>扩展到3.0 cm, VPI可归为IIA期。因此,考虑术后化疗的患者队列可能是有保证的。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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