Radiomics in predicting treatment response in non-small-cell lung cancer: current status, challenges and future perspectives

被引:149
|
作者
Chetan, Madhurima R. [1 ,2 ]
Gleeson, Fergus V. [1 ,3 ]
机构
[1] Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Churchill Hosp, Old Rd, Oxford OX3 7LE, England
[2] Univ Oxford, Nuffield Dept Surg Sci, John Radcliffe Hosp, Room 6607,Level 6, Oxford OX3 9DU, England
[3] Univ Oxford, Dept Oncol, Old Rd Campus Res Bldg,Roosevelt Dr, Oxford OX3 7DQ, England
关键词
Carcinoma; non-small-cell lung; Tomography; X-ray computed; Positron emission tomography computed tomography; Biomarkers; Precision medicine; POSITRON-EMISSION-TOMOGRAPHY; PATHOLOGICAL RESPONSE; CHEMOTHERAPY; ERLOTINIB; SURVIVAL; FEATURES; TUMORS; NSCLC;
D O I
10.1007/s00330-020-07141-9
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
Objectives Radiomics is the extraction of quantitative data from medical imaging, which has the potential to characterise tumour phenotype. The radiomics approach has the capacity to construct predictive models for treatment response, essential for the pursuit of personalised medicine. In this literature review, we summarise the current status and evaluate the scientific and reporting quality of radiomics research in the prediction of treatment response in non-small-cell lung cancer (NSCLC). Methods A comprehensive literature search was conducted using the PubMed database. A total of 178 articles were screened for eligibility and 14 peer-reviewed articles were included. The radiomics quality score (RQS), a radiomics-specific quality metric emulating the TRIPOD guidelines, was used to assess scientific and reporting quality. Results Included studies reported several predictive markers including first-, second- and high-order features, such as kurtosis, grey-level uniformity and wavelet HLL mean respectively, as well as PET-based metabolic parameters. Quality assessment demonstrated a low median score of + 2.5 (range - 5 to + 9), mainly reflecting a lack of reproducibility and clinical evaluation. There was extensive heterogeneity between studies due to differences in patient population, cancer stage, treatment modality, follow-up timescales and radiomics workflow methodology. Conclusions Radiomics research has not yet been translated into clinical use. Efforts towards standardisation and collaboration are needed to identify reproducible radiomic predictors of response. Promising radiomic models must be externally validated and their impact evaluated within the clinical pathway before they can be implemented as a clinical decision-making tool to facilitate personalised treatment for patients with NSCLC.
引用
收藏
页码:1049 / 1058
页数:10
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