A potential biomarker based on clinical-radiomics nomogram for predicting survival and adjuvant chemotherapy benefit in resected node-negative, early-stage lung adenocarcinoma

被引:1
|
作者
Ma, Xiaoling [1 ]
Lv, Wenzhi [2 ]
Wang, Cong [3 ]
Tu, Dehao [4 ]
Qiao, Jinhan [1 ]
Fan, Chanyuan [1 ]
Niu, Jiandong [5 ]
Zhou, Wen [1 ]
Liu, Qiuyu [1 ]
Xia, Liming [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Radiol, 1095 Jiefang Rd, Wuhan 430030, Peoples R China
[2] Julei Technol Co, Dept Artificial Intelligence, Wuhan, Peoples R China
[3] Chinese Acad Sci, Suzhou Inst Biomed Engn & Technol, Jiangsu Key Lab Med Opt, Suzhou, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Thorac Surg, Wuhan, Peoples R China
[5] Ningxia Med Univ, Gen Hosp, Dept Radiol, Yinchuan, Ningxia, Peoples R China
基金
中国国家自然科学基金;
关键词
Adjuvant chemotherapy (ACT); radiomics; survival; lung adenocarcinoma (lung ADC); computer tomography; VINORELBINE PLUS CISPLATIN; CT TEXTURE ANALYSIS; CANCER; IIIA; ASSOCIATION; SIGNATURE; THERAPY;
D O I
10.21037/jtd-21-1520
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: We aimed to construct a clinical-radiomics nomogram to predict disease-free survival (DFS) and the added survival benefit of adjuvant chemotherapy (ACT) for node-negative, early-stage (I-II) lung adenocarcinoma (ADC). Methods: In this retrospective study including 310 patients from two independent cohorts, the CTderived radiomics features were selected by least absolute shrinkage and selection operator Cox regression to generate a radiomics signature associated with DFS. The radiomics signature was incorporated to construct a clinical-radiomics nomogram along with the independent clinical risk predictors. The model performance was evaluated with reference to discrimination quantified by Harrell concordance index (C-index), integrated discrimination improvement (IDI) and net reclassification index (NRI), calibration and clinical utility. The risk score (RS) for clinical-radiomics nomogram was calculated. The association between ACT and survival benefit was assessed in high and low RS subgroup. Results: The clinical-radiomics nomogram achieved the highest C-index of 0.822 [95% confidence interval (CI): 0.769, 0.876] in training cohort and 0.802 (95% CI: 0.716, 0.888) in validation cohort. The incorporation of radiomics signature into clinical-radiomics nomogram showed an incremental benefit over clinical nomogram according to the improved NRI and IDI. The calibration curves and decision curve analysis further verified the clinical utility of clinical-radiomics nomogram. Further, patients with high RS based on clinical-radiomics nomogram were more prone to benefit from ACT. Conclusions: The clinical-radiomics nomogram approach can feasibly conduct risk prediction and have potential to identify the beneficiaries of ACT among patients with node-negative, early-stage ADC, which might serve as a helpful tool in informing therapeutic decision-making.
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页码:1 / +
页数:19
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