Real-world comprehensive diagnosis and "Surgery plus X" treatment strategy of early-stage synchronous multiple primary lung cancer

被引:14
作者
Zhou, Danting [1 ,2 ]
Yao, Tianyu [1 ,2 ]
Huang, Xiaojie [1 ]
Wu, Fang [3 ]
Jiang, Yi [4 ]
Peng, Muyun [1 ,2 ]
Qian, Banglun [1 ,2 ]
Liu, Wenliang [1 ,2 ]
Yu, Fenglei [1 ,2 ]
Chen, Chen [1 ,2 ,5 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Thorac Surg, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Hunan Key Lab Early Diag & Precise Treatment Lung, Changsha 410011, Peoples R China
[3] Cent South Univ, Xiangya Hosp 2, Dept Oncol, Changsha, Hunan, Peoples R China
[4] Cent South Univ, Xiangya Hosp 2, Dept Pathol, Changsha, Hunan, Peoples R China
[5] Cent South Univ, Xiangya Hosp 2, Dept Thorac Surg, Hunan Key Lab Early Diag & Precise Treatment Lung, Changsha 410011, Peoples R China
来源
CANCER MEDICINE | 2023年 / 12卷 / 12期
关键词
ablation; early-stage; EGFR-TKIs; gene mutation; SBRT; surgery; synchronous multiple primary lung cancers; SPECIAL TREATMENT ISSUES; GLASS OPACITY COMPONENT; PROGNOSTIC IMPACT; 8TH EDITION; ADENOCARCINOMA; CLASSIFICATION;
D O I
10.1002/cam4.5972
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Diagnosing and treating synchronous multiple primary lung cancers (sMPLC) are complex and challenging. This study aimed to report real-world data on the comprehensive diagnosis and treatment of patients with early-stage sMPLC.Materials and Methods A single-center cohort study was carried out and a large number of patients with early-stage sMPLC were included. A single- or two-stage surgery was performed to remove the primary and co-existing lesions. The "X" strategies, including ablation, SBRT, and EGFR-TKIs treatment, were applied to treat the high-risk residual lesions. Wide panel-genomic sequencing was performed to assess the genetic heterogeneity of the co-existing lesions.Results A total of 465 early-stage sMPLC patients with 1198 resected lesions were included. Despite most patients being histologically different or harboring different genetic alternations, about 7.5% of the patients had the same histological type and driver gene mutation changes, comprehensive re-evaluation is thus needed. The "Surgery + X" strategy showed remarkable efficacy and safety in treating multiple lesions. Follow-up data revealed that the T2 stage (p = 0.014) and the solid presence of a primary lesion (p < 0.001) were significantly related to tumor recurrence. And a T2-stage primary tumor had a significantly higher rate of developing new lesions after the initial surgery (p < 0.001).Conclusions In real-world practice, histopathological and radiological evaluation combined with genetic analyses could be a robust diagnostic approach for sMPLC. The "Surgery + X" treatment strategy showed remarkable efficacy, superiority, and safety in the clinical treatment of early-stage sMPLC.
引用
收藏
页码:12996 / 13006
页数:11
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