Clinical Significance of a Circulating Tumor Cell-based Classifier in Stage IB Lung Adenocarcinoma A Multicenter, Cohort Study

被引:6
|
作者
Ren, Lijuan [1 ]
Zhong, Xiaoming [2 ]
Liu, Wei [2 ]
Xu, Di [3 ]
Lei, Yiyan [4 ]
Zhou, Jianwen [1 ]
Jiang, Wenting [1 ]
He, Qiong [1 ]
Sun, Yu [1 ]
Ke, Zunfu [1 ,5 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Mol Diag & Gene Testing Ctr, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Sch Med, Guangzhou, Peoples R China
[3] Huazhong Univ Sci & Technol, Cent Hosp Wuhan, Tongji Med Coll, Dept Thorac Surg, Wuhan, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Thorac Surg, Guangzhou, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 1, Inst Precis Med, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
aptamer; circulating tumor cell; prognosis; stage IB lung adenocarcinoma; ADJUVANT CHEMOTHERAPY; CANCER; SIGNATURE; PROGRESSION; CISPLATIN; SURVIVAL; SURGERY; BENEFIT; MARKER;
D O I
10.1097/SLA.0000000000004780
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective:To investigate the effectiveness of a CTC-based classifier in stratifying stage IB LUAD. Summary of Background Data:Stage IB LUADs have an approximately 70% 5-year survival rate. The clinical application of ACT is controversial due to inconsistent results in a series of trials and few useful guide biomarkers. Thus, there is a pressing need for robust biomarkers to stratify stage IB patients to define which group would most likely benefit from ACT. Methods: Two hundred twelve stage IB LUAD patients were enrolled and were divided into 3 independent cohorts. The aptamer-modified NanoVelcro system was used to enrich the CTCs. Results:A cutoff of 4 CTCs as the optimal prognostic threshold for stage IB LUAD was generated to stratify the patients in a 70-patient cohort into low-risk and high-risk groups. Patients with >= 4 CTCs in the training cohort had shorter progression-free survival (P < 0.0001) and overall survival (P < 0.0001) than patients with <4 CTCs. CTC number remained the strongest predictor of progression-free survival and overall survival even in a multivariate analysis including other clinicopathological parameters. Furthermore, a nomogram based on the CTC count was developed to predict the 3-year and 5-year survival in the training cohort and performed well in the other 2 validation cohorts (C-index: 0.862, 0.853, and 0.877). Conclusion:The presence of >4 CTCs can define a high-risk subgroup, providing a new strategy to make optimal clinical decisions for stage IB LUAD.
引用
收藏
页码:E439 / E448
页数:10
相关论文
共 50 条
  • [1] Clinical Validation of LungLB: A Circulating Genetically Abnormal Cell-Based Classifier for Indeterminate Lung Nodule Evaluation
    Pagano, P.
    Henschke, C.
    Abudara, M.
    Salehi-Rad, R.
    Reid, M.
    Yankelevitz, D.
    Covey, A.
    Ghandehari, S.
    Hassan, Z.
    Kuban, J.
    Clum, S.
    Czerlanis, C.
    Dixon, J.
    Ghori, U.
    Mahajan, A.
    Tahvilian, S.
    Katchman, B.
    Lutman, M.
    Gramajo-Leventon, D.
    Baden, L.
    Slavatore, M.
    Schwartz, L.
    Kattan, M.
    Vail, E.
    Donovan, M.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2024, 26 (11): : S111 - S111
  • [2] Survival Prediction and Adjuvant Chemotherapy Based on Tumor Marker for Stage IB Lung Adenocarcinoma
    Wang, Yiyang
    Zheng, Difan
    Chen, Tianxiang
    Zhang, Jie
    Yao, Feng
    Chen, Haiquan
    ANNALS OF THORACIC SURGERY, 2020, 109 (03): : 927 - 937
  • [3] Biology and clinical significance of circulating tumor cell subpopulations in lung cancer
    O'Flaherty, Linda
    Wikman, Harriet
    Pantel, Klaus
    TRANSLATIONAL LUNG CANCER RESEARCH, 2017, 6 (04) : 431 - 443
  • [4] Stage I Lung Adenocarcinoma Tumor Density And Contour Do Not Predict Circulating Tumor Cell Burden
    Nair, V. S.
    Luttgen, M.
    Keu, K.
    Jamali, M.
    Horng, G.
    Vasanawala, M.
    Kuschner, W.
    Shrager, J.
    Kuhn, P.
    Gambhir, S. S.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 189
  • [5] A proof-of-concept study for the clinical utility of a circulating tumor cell-based mutation analysis
    Franken, A.
    Behrens, B.
    Reinhardt, F.
    Yang, L.
    Rivandi, M.
    Cieslik, J. P.
    Dietzel, F.
    Stoecklein, N. H.
    Niederacher, D.
    Fehmt, T.
    Neubauer, H.
    GEBURTSHILFE UND FRAUENHEILKUNDE, 2020, 80 (10) : E97 - E97
  • [6] Deep learning model based on primary tumor to predict lymph node status in clinical stage IA lung adenocarcinoma: a multicenter study
    Zhang, Li
    Li, Hailin
    Zhao, Shaohong
    Tao, Xuemin
    Li, Meng
    Yang, Shouxin
    Zhou, Lina
    Liu, Mengwen
    Zhang, Xue
    Dong, Di
    Tian, Jie
    Wu, Ning
    JOURNAL OF THE NATIONAL CANCER CENTER, 2024, 4 (03): : 233 - 240
  • [7] Mast cell-based molecular subtypes and signature associated with clinical outcome in early-stage lung adenocarcinoma
    Bao, Xuanwen
    Shi, Run
    Zhao, Tianyu
    Wang, Yanfang
    MOLECULAR ONCOLOGY, 2020, 14 (05) : 917 - 932
  • [8] Clinical significance of circulating tumor cells in squamous cell lung cancer patients
    Qi, Yuanling
    Wang, Wenhui
    CANCER BIOMARKERS, 2017, 18 (02) : 161 - 167
  • [9] Clinical correlations with EGFR circulating tumor DNA testing in all-stage lung adenocarcinoma
    Incharoen, Pimpin
    Jinawath, Artit
    Arsa, Lalida
    Kamprerasart, Kaettipong
    Trachu, Narumol
    Monnamo, Nanamon
    Khiewngam, Khantong
    Muntham, Dittapol
    Chansriwong, Phichai
    Sirachainan, Ekaphop
    Reungwetwattana, Thanyanan
    CANCER BIOMARKERS, 2023, 36 (01) : 71 - 82
  • [10] Clinical Significance of Red Cell Distribution Width and Circulating Tumor Cells with an Epithelial-Mesenchymal Transition Phenotype in Lung Adenocarcinoma
    Peng, Huajian
    Tan, Xiang
    Wang, Yongyong
    Dai, Lei
    Liang, Guanbiao
    Guo, Jianji
    Chen, Mingwu
    CANCER MANAGEMENT AND RESEARCH, 2020, 12 : 5105 - 5117