Evidence map›Paper›PMID 35109864›Full record

Trial reportJournal of translational medicine2022

Radiomic analysis for predicting prognosis of colorectal cancer from preoperative

Lilang Lv, Bowen Xin, Yichao Hao, Ziyi Yang, Junyan Xu, Lisheng Wang, Xiuying Wang, Shaoli Song, Xiaomao Guo

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed.

  1. Review
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  12. AAbdominal radiology (New York) · 2025
    Article
  13. Added value of dual-phaseFrontiers in oncology · 2025
    Article
  14. Article
  15. Review
  16. Article
  17. [Cancer imaging : the official publication of the International Cancer Imaging Society · 2024
    Article
  18. Review
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  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Lilang Lv *Department of Radiotherapy, Fudan University Shanghai Cancer Center, No.270 Dong'an Road, Xuhui district, Shanghai, 200032, China.
Bowen Xin *School of Computer Science, The University of Sydney, Sydney, NSW, Australia.
Yichao Hao *School of Computer Science, The University of Sydney, Sydney, NSW, Australia.
Ziyi YangDepartment of Nuclear Medicine, Fudan University Shanghai Cancer Center, No.270 Dong'an Road, Xuhui district, Shanghai, 200032, China.
Junyan XuDepartment of Nuclear Medicine, Fudan University Shanghai Cancer Center, No.270 Dong'an Road, Xuhui district, Shanghai, 200032, China.
Lisheng WangDepartment of Automation, Shanghai Jiao Tong University, Shanghai, 200240, China.
Xiuying WangSchool of Computer Science, The University of Sydney, Sydney, NSW, Australia.
Shaoli SongDepartment of Nuclear Medicine, Fudan University Shanghai Cancer Center, No.270 Dong'an Road, Xuhui district, Shanghai, 200032, China. shaoli-song@163.com.
Xiaomao GuoDepartment of Radiotherapy, Fudan University Shanghai Cancer Center, No.270 Dong'an Road, Xuhui district, Shanghai, 200032, China. guoxm1800@126.com.

Funding

National Natural Science Foundation of China 81771861National Natural Science Foundation of China 81971648Shanghai Scientific and Technological Innovation Program 18410711200Shanghai Scientific and Technological Innovation Program 19142202100
6 · The paper itself

Abstract

backgroundTo develop and validate a survival model with clinico-biological features and

methodsA total of 196 pathologically confirmed patients with colorectal cancer (stage I to stage IV) were included. Preoperative clinical factors, serum tumor markers, and PET/CT radiomic features were included for the recurrence-free survival analysis. For the modeling and validation, patients were randomly divided into the training (n = 137) and validation (n = 59) set, while the 78 stage III patients [training (n = 55), and validation (n = 23)] was divided for the further experiment. After selecting features by the log-rank test and variable-hunting methods, random survival forest (RSF) models were built on the training set to analyze the prognostic value of selected features. The performance of models was measured by C-index and was tested on the validation set with bootstrapping. Feature importance and the Pearson correlation were also analyzed.

resultsRadiomics signature (containing four PET/CT features and four clinical factors) achieved the best result for prognostic prediction of 196 patients (C-index 0.780, 95% CI 0.634-0.877). Moreover, four features (including two clinical features and two radiomics features) were selected for prognostic prediction of the 78 stage III patients (C-index was 0.820, 95% CI 0.676-0.900). K-M curves of both models significantly stratified low-risk and high-risk groups (P < 0.0001). Pearson correlation analysis demonstrated that selected radiomics features were correlated with tumor metabolic factors, such as SUVmean, SUVmax.

conclusionThis study presents integrated clinico-biological-radiological models that can accurately predict the prognosis in colorectal cancer using the preoperative

Indexed as

Colorectal NeoplasmsPositron Emission Tomography Computed TomographyChinaFluorodeoxyglucose F18HumansPrognosisFluorodeoxyglucose F1818F-FDG PET/CTPredictionPrognosisRadiomicsStage III Colorectal cancer

Identifiers

PMID35109864
PMCPMC8812058

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.