Prediction of p53 mutation status in rectal cancer patients based on magnetic resonance imaging-based nomogram: a study of machine learning

被引:3
作者
Zhong, Xia [1 ]
Peng, Jiaxuan [2 ]
Shu, Zhenyu [3 ]
Song, Qiaowei [3 ]
Li, Dongxue [3 ]
机构
[1] Zhejiang Chinese Med Univ, Clin Med Coll 1, Hangzhou, Zhejiang, Peoples R China
[2] Jinzhou Med Univ, Jinzhou, Liaoning, Peoples R China
[3] Zhejiang Prov Peoples Hosp, Affiliated Peoples Hosp, Hangzhou Med Coll, Canc Ctr,Dept Radiol, Hangzhou, Zhejiang, Peoples R China
关键词
Nomogram; Rectal cancer; Machine learning; p53; gene; Magnetic resonance imaging; FEATURES; TUMOR; EXPRESSION; PROTEIN;
D O I
10.1186/s40644-023-00607-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe current study aimed to construct and validate a magnetic resonance imaging (MRI)-based radiomics nomogram to predict tumor protein p53 gene status in rectal cancer patients using machine learning.MethodsClinical and imaging data from 300 rectal cancer patients who underwent radical resections were included in this study, and a total of 166 patients with p53 mutations according to pathology reports were included in these patients. These patients were allocated to the training (n = 210) or validation (n = 90) cohorts (7:3 ratio) according to the examination time. Using the training data set, the radiomic features of primary tumor lesions from T2-weighted images (T2WI) of each patient were analyzed by dimensionality reduction. Multivariate logistic regression was used to screen predictive features, which were combined with a radiomics model to construct a nomogram to predict p53 gene status. The accuracy and reliability of the nomograms were assessed in both training and validation data sets using receiver operating characteristic (ROC) curves.ResultsUsing the radiomics model with the training and validation cohorts, the diagnostic efficacies were 0.828 and 0.795, the sensitivities were 0.825 and 0.891, and the specificities were 0.722 and 0.659, respectively. Using the nomogram with the training and validation data sets, the diagnostic efficacies were 0.86 and 0.847, the sensitivities were 0.758 and 0.869, and the specificities were 0.833 and 0.75, respectively.ConclusionsThe radiomics nomogram based on machine learning was able to predict p53 gene status and facilitate preoperative molecular-based pathological diagnoses.
引用
收藏
页数:11
相关论文
共 31 条
[1]   Decoding tumour phenotype by noninvasive imaging using a quantitative radiomics approach [J].
Aerts, Hugo J. W. L. ;
Velazquez, Emmanuel Rios ;
Leijenaar, Ralph T. H. ;
Parmar, Chintan ;
Grossmann, Patrick ;
Cavalho, Sara ;
Bussink, Johan ;
Monshouwer, Rene ;
Haibe-Kains, Benjamin ;
Rietveld, Derek ;
Hoebers, Frank ;
Rietbergen, Michelle M. ;
Leemans, C. Rene ;
Dekker, Andre ;
Quackenbush, John ;
Gillies, Robert J. ;
Lambin, Philippe .
NATURE COMMUNICATIONS, 2014, 5
[2]   The predictive value of p53 and p33ING1b in patients with Dukes'C colorectal cancer [J].
Ahmed, I. A. M. ;
Kelly, S. B. ;
Anderson, J. J. ;
Angus, B. ;
Challen, C. ;
Lunec, J. .
COLORECTAL DISEASE, 2008, 10 (04) :344-351
[3]   Wild type- and mutant p53 proteins in mitochondrial dysfunction: emerging insights in cancer disease [J].
Blandino, Giovanni ;
Valenti, Fabio ;
Sacconi, Andrea ;
Di Agostino, Silvia .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2020, 98 :105-117
[4]   P53 Status as a Predictive Biomarker for Patients Receiving Neoadjuvant Radiation-Based Treatment: A Meta-Analysis in Rectal Cancer [J].
Chen, Min-Bin ;
Wu, Xiao-Yang ;
Yu, Rong ;
Li, Chen ;
Wang, Li-Qiang ;
Shen, Wei ;
Lu, Pei-Hua .
PLOS ONE, 2012, 7 (09)
[5]   Rectal Cancer in Asian vs. Western Countries: Why the Variation in Incidence? [J].
Deng, Yanhong .
CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2017, 18 (10)
[6]   MRI cT1-2 rectal cancer staging accuracy: a population-based study [J].
Detering, R. ;
van Oostendorp, S. E. ;
Meyer, V. M. ;
van Dieren, S. ;
Bos, A. C. R. K. ;
Dekker, J. W. T. ;
Reerink, O. ;
van Waesberghe, J. H. T. M. ;
Marijnen, C. A. M. ;
Moons, L. M. G. ;
Beets-Tan, R. G. H. ;
Hompes, R. ;
van Westreenen, H. L. ;
Tanis, P. J. ;
Tuynman, J. B. .
BRITISH JOURNAL OF SURGERY, 2020, 107 (10) :1372-1382
[7]  
Gao Y, 2021, Phys Med Biol, V66
[8]  
Gasinska A, 2017, REP PRACT ONCOL RADI, V22, P368, DOI 10.1016/j.rpor.2017.07.002
[9]   Targeting Tumor Suppressor p53 for Cancer Therapy: Strategies, Challenges and Opportunities [J].
Hong, Bo ;
van den Heuvel, A. Pieter J. ;
Prabhu, Varun V. ;
Zhang, Shengliang ;
El-Deiry, Wafik S. .
CURRENT DRUG TARGETS, 2014, 15 (01) :80-89
[10]   Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer [J].
Iwatate, Yosuke ;
Hoshino, Isamu ;
Yokota, Hajime ;
Ishige, Fumitaka ;
Itami, Makiko ;
Mori, Yasukuni ;
Chiba, Satoshi ;
Arimitsu, Hidehito ;
Yanagibashi, Hiroo ;
Nagase, Hiroki ;
Takayama, Wataru .
BRITISH JOURNAL OF CANCER, 2020, 123 (08) :1253-1261