Early survival prediction in non-small cell lung cancer from PET/CT images using an intra-tumor partitioning method

被引:38
作者
Astaraki, Mehdi [1 ,2 ]
Wang, Chunliang [1 ]
Buizza, Giulia [3 ]
Toma-Dasu, Iuliana [2 ,4 ]
Lazzeroni, Marta [2 ,4 ]
Smedby, Orjan [1 ]
机构
[1] KTH Royal Inst Technol, Dept Biomed Engn & Hlth Syst, Halsovagen 11C, SE-14157 Huddinge, Sweden
[2] Karolinska Inst, Dept Oncol Pathol, Karolinska Univ Sjukhuset, SE-17176 Stockholm, Sweden
[3] Politecn Milan, Dept Elect Informat & Bioengn, Piazza Leonardo da Vinci 42, I-20133 Milan, Italy
[4] Stockholm Univ, Dept Phys, SE-10691 Stockholm, Sweden
来源
PHYSICA MEDICA-EUROPEAN JOURNAL OF MEDICAL PHYSICS | 2019年 / 60卷
关键词
Survival prediction; Treatment response; Radiomics; Tumor heterogeneity; POSITRON-EMISSION-TOMOGRAPHY; FDG-PET; PROGNOSTIC VALUE; PATHOLOGICAL RESPONSE; RADIOMICS SIGNATURE; METABOLIC-RESPONSE; QUANTITATIVE IMAGE; TEXTURE FEATURES; TEST-RETEST; STAGE I;
D O I
10.1016/j.ejmp.2019.03.024
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To explore prognostic and predictive values of a novel quantitative feature set describing intra-tumor heterogeneity in patients with lung cancer treated with concurrent and sequential chemoradiotherapy. Methods: Longitudinal PET-CT images of 30 patients with non-small cell lung cancer were analysed. To describe tumor cell heterogeneity, the tumors were partitioned into one to ten concentric regions depending on their sizes, and, for each region, the change in average intensity between the two scans was calculated for PET and CT images separately to form the proposed feature set. To validate the prognostic value of the proposed method, radiomics analysis was performed and a combination of the proposed novel feature set and the classic radiomic features was evaluated. A feature selection algorithm was utilized to identify the optimal features, and a linear support vector machine was trained for the task of overall survival prediction in terms of area under the receiver operating characteristic curve (AUROC). Results: The proposed novel feature set was found to be prognostic and even outperformed the radiomics approach with a significant difference (AUROC(sALop) = 0.90 vs. AUROC(radiomic) = 0.71) when feature selection was not employed, whereas with feature selection, a combination of the novel feature set and radiomics led to the highest prognostic values. Conclusion: A novel feature set designed for capturing intra-tumor heterogeneity was introduced. Judging by their prognostic power, the proposed features have a promising potential for early survival prediction.
引用
收藏
页码:58 / 65
页数:8
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