Evidence map›Paper›PMID 34868946›Full record

ArticleFrontiers in oncology2021

Automated Classification of Papillary Renal Cell Carcinoma and Chromophobe Renal Cell Carcinoma Based on a Small Computed Tomography Imaging Dataset Using Deep Learning.

Teng Zuo, Yanhua Zheng, Lingfeng He, Tao Chen, Bin Zheng, Song Zheng, Jinghang You, Xiaoyan Li, Rong Liu, Junjie Bai and 5 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

15 authors.

Teng ZuoDepartment of Urology, Fujian Medical University Union Hospital, Fuzhou, China.
Yanhua ZhengDepartment of Urology, Fujian Medical University Union Hospital, Fuzhou, China.
Lingfeng HeInstitute for Empirical Social Science Research, Xi'an Jiaotong University, Xi'an, China.
Tao ChenSchool of Statistics and Mathematics, Central University of Finance and Economics, Beijing, China.
Bin ZhengSchool of Electrical and Computer Engineering, University of Oklahoma, Norman, OK, United States.
Song ZhengDepartment of Urology, Fujian Medical University Union Hospital, Fuzhou, China.
Jinghang YouDepartment of Radiology, Fujian Medical University Union Hospital, Fuzhou, China.
Xiaoyan LiDepartment of Pathology, Fujian Medical University Union Hospital, Fuzhou, China.
Rong LiuDepartment of Urology, Fujian Medical University Union Hospital, Fuzhou, China.
Junjie BaiDepartment of Urology, Fujian Medical University Union Hospital, Fuzhou, China.
Shuxin SiDepartment of Urology, Fujian Medical University Union Hospital, Fuzhou, China.
Yingying WangSchool of Medicine, Fujian Medical University, Fuzhou, China.
Shuyi ZhangSchool of Medicine, Xiamen University, Xiamen, China.
Lili WangSchool of Electrical and Computer Engineering, University of Oklahoma, Norman, OK, United States.
Jianhui ChenDepartment of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study was conducted in order to design and develop a framework utilizing deep learning (DL) to differentiate papillary renal cell carcinoma (PRCC) from chromophobe renal cell carcinoma (ChRCC) using convolutional neural networks (CNNs) on a small set of computed tomography (CT) images and provide a feasible method that can be applied to light devices.

methodsTraining and validation datasets were established based on radiological, clinical, and pathological data exported from the radiology, urology, and pathology departments. As the gold standard, reports were reviewed to determine the pathological subtype. Six CNN-based models were trained and validated to differentiate the two subtypes. A special test dataset generated with six new cases and four cases from The Cancer Imaging Archive (TCIA) was applied to validate the efficiency of the best model and of the manual processing by abdominal radiologists. Objective evaluation indexes [accuracy, sensitivity, specificity, receiver operating characteristic (ROC) curve, and area under the curve (AUC)] were calculated to assess model performance.

resultsThe CT image sequences of 70 patients were segmented and validated by two experienced abdominal radiologists. The best model achieved 96.8640% accuracy (99.3794% sensitivity and 94.0271% specificity) in the validation set and 100% (case accuracy) and 93.3333% (image accuracy) in the test set. The manual classification achieved 85% accuracy (100% sensitivity and 70% specificity) in the test set.

conclusionsThis framework demonstrates that DL models could help reliably predict the subtypes of PRCC and ChRCC.

Indexed as

cancer image classificationChRCC,·chromophobe-primary renal cell carcinomaCNN—convolutional neural networkpapillary renal cell carcinomaPRCC

Identifiers

PMID34868946
PMCPMC8637858

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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.