Nomograms integrating CT radiomic and deep learning signatures to predict overall survival and progression-free survival in NSCLC patients treated with chemotherapy

被引:1
作者
Chang, Runsheng [1 ]
Qi, Shouliang [1 ,2 ]
Wu, Yanan [1 ]
Yue, Yong [3 ]
Zhang, Xiaoye [4 ]
Qian, Wei [1 ]
机构
[1] Northeastern Univ, Coll Med & Biol Informat Engn, Shenyang, Peoples R China
[2] Northeastern Univ, Key Lab Intelligent Comp Med Image, Minist Educ, Shenyang, Peoples R China
[3] China Med Univ, Shengjing Hosp, Dept Radiol, Shenyang, Peoples R China
[4] China Med Univ, Shengjing Hosp, Dept Oncol, Shenyang, Peoples R China
关键词
Nomogram; Overall survival; Progression-free survival; Lung cancer; Chemotherapy treatment; Radiomics; CELL LUNG-CANCER; IMMUNE CHECKPOINT INHIBITORS; TUMOR HETEROGENEITY; STAGING PROJECT; ASSOCIATION; EVOLUTION;
D O I
10.1186/s40644-023-00620-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ObjectivesThis study aims to establish nomograms to accurately predict the overall survival (OS) and progression-free survival (PFS) in patients with non-small cell lung cancer (NSCLC) who received chemotherapy alone as the first-line treatment.Materials and methodsIn a training cohort of 121 NSCLC patients, radiomic features were extracted, selected from intra- and peri-tumoral regions, and used to build signatures (S1 and S2) using a Cox regression model. Deep learning features were obtained from three convolutional neural networks and utilized to build signatures (S3, S4, and S5) that were stratified into over- and under-expression subgroups for survival risk using X-tile. After univariate and multivariate Cox regression analyses, a nomogram incorporating the tumor, node, and metastasis (TNM) stages, radiomic signature, and deep learning signature was established to predict OS and PFS, respectively. The performance was validated using an independent cohort (61 patients).ResultsTNM stages, S2 and S3 were identified as the significant prognosis factors for both OS and PFS; S2 (OS: (HR (95%), 2.26 (1.40-3.67); PFS: (HR (95%), 2.23 (1.36-3.65)) demonstrated the best ability in discriminating patients with over- and under-expression. For the OS nomogram, the C-index (95% CI) was 0.74 (0.70-0.79) and 0.72 (0.67-0.78) in the training and validation cohorts, respectively; for the PFS nomogram, the C-index (95% CI) was 0.71 (0.68-0.81) and 0.72 (0.66-0.79). The calibration curves for the 3- and 5-year OS and PFS were in acceptable agreement between the predicted and observed survival. The established nomogram presented a higher overall net benefit than the TNM stage for predicting both OS and PFS.ConclusionBy integrating the TNM stage, CT radiomic signature, and deep learning signatures, the established nomograms can predict the individual prognosis of NSCLC patients who received chemotherapy. The integrated nomogram has the potential to improve the individualized treatment and precise management of NSCLC patients. Integrated nomograms aim to predict the chemotherapy prognosis of NSCLC patients.The 3- and 5-year overall survival and progression-free survival are predicted.CT peritumoral radiomic signature has the highest hazard ratio for the prognosis.Deep learning signature is a significant predictive factor of the prognosis.The integrated nomograms are noninvasive, low cost, and phenotypic.
引用
收藏
页数:12
相关论文
共 48 条
  • [1] [Anonymous], 2009, J THORAC ONCOL
  • [2] Balachandran VP, 2013, Nomograms in oncology: more than meets the eye
  • [3] Tumour heterogeneity and the evolution of polyclonal drug resistance
    Burrell, Rebecca A.
    Swanton, Charles
    [J]. MOLECULAR ONCOLOGY, 2014, 8 (06): : 1095 - 1111
  • [4] X-tile: A new bio-informatics tool for biomarker assessment and outcome-based cut-point optimization
    Camp, RL
    Dolled-Filhart, M
    Rimm, DL
    [J]. CLINICAL CANCER RESEARCH, 2004, 10 (21) : 7252 - 7259
  • [5] Predicting chemotherapy response in non-small-cell lung cancer via computed tomography radiomic features: Peritumoral, intratumoral, or combined?
    Chang, Runsheng
    Qi, Shouliang
    Zuo, Yifan
    Yue, Yong
    Zhang, Xiaoye
    Guan, Yubao
    Qian, Wei
    [J]. FRONTIERS IN ONCOLOGY, 2022, 12
  • [6] The International Association for the Study of Lung Cancer Staging Project Prognostic Factors and Pathologic TNM Stage in Surgically Managed Non-small Cell Lung Cancer
    Chansky, Kari
    Sculier, Jean-Paul
    Crowley, John J.
    Giroux, Dori
    Van Meerbeeck, Jan
    Goldstraw, Peter
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (07) : 792 - 801
  • [7] Intratumoral and peritumoral radiomics nomograms for the preoperative prediction of lymphovascular invasion and overall survival in non-small cell lung cancer
    Chen, Qiaoling
    Shao, JingJing
    Xue, Ting
    Peng, Hui
    Li, Manman
    Duan, Shaofeng
    Feng, Feng
    [J]. EUROPEAN RADIOLOGY, 2023, 33 (02) : 947 - 958
  • [8] Survival of patients treated surgically for synchronous single-organ metastatic NSCLC and advanced pathologic TN stage
    Collaud, Stephane
    Stahel, Rolf
    Inci, Ilhan
    Hillinger, Sven
    Schneiter, Didier
    Kestenholz, Peter
    Weder, Walter
    [J]. LUNG CANCER, 2012, 78 (03) : 234 - 238
  • [9] Immune checkpoint inhibitors, alone or in combination with chemotherapy, as first-line treatment for advanced non-small cell lung cancer. A systematic review and network meta-analysis
    Dafni, Urania
    Tsourti, Zoi
    Vervita, Katerina
    Peters, Solange
    [J]. LUNG CANCER, 2019, 134 : 127 - 140
  • [10] Construction of a nomogram predicting the overall survival of patients with distantly metastatic non-small-cell lung cancer
    Deng, Jianqing
    Ren, Zhipeng
    Wen, Jiaxin
    Wang, Bo
    Hou, Xiaobin
    Xue, Zhiqiang
    Chu, Xiangyang
    [J]. CANCER MANAGEMENT AND RESEARCH, 2018, 10 : 6143 - 6156