Evidence map›Paper›PMID 40332632›Full record

ArticleMedical & biological engineering & computing2025

Deep learning-based prognostic assessment of polyploid giant cancer cells and mitotic figures in liver cancer.

Jingying Yang, Cuimin Chen, Qiming He, Jiayi Li, Houqiang Li, Jing Peng, Junru Cheng, Meihui Li, Xiaozhuan Zhou, Yonghong He and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Medical & biological engineering & computing, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

13 authors.

Jingying Yang *Department of Life and Health, Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.
Cuimin Chen *Department of Pathology, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Qiming He *Department of Life and Health, Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.
Jiayi Li *Department of Life and Health, Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.
Houqiang LiShengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Jing PengDepartment of Life and Health, Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.
Junru ChengDepartment of Life and Health, Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.
Meihui LiShenzhen University, Shenzhen, 518055, China.
Xiaozhuan ZhouDepartment of Gastroenterology, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Yonghong HeDepartment of Life and Health, Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.
Tian GuanDepartment of Life and Health, Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China. guantian@sz.tsinghua.edu.cn.
Xi LiDepartment of Gastroenterology, Peking University Shenzhen Hospital, Shenzhen, 518036, China. lixi122188@sina.com.
Danling JiangDepartment of Gastroenterology, Peking University Shenzhen Hospital, Shenzhen, 518036, China. danlingjiang@foxmail.com.

Funding

Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Province KCXFZ20201221173207022Science and Technology Research Program of Shenzhen City WDZC2020200821141349001
6 · The paper itself

Abstract

Primary liver cancer is among the most lethal malignancies, with cell-level structural features such as polyploid giant cancer cells and mitotic figures strongly associated with poor patient prognosis. However, the quantification of these features is hindered by a shortage of pathologists, high workloads, and subjective discrepancies. To address these challenges, we leverage deep learning algorithms to enable the rapid detection of cell-level features, combining this capability with survival analysis to establish a novel, practical prognostic risk assessment system for liver cancer diagnosis and treatment. In collaboration with Peking University Shenzhen Hospital, we collected 172 liver cancer cases, comprising 340 pathology images, to construct the HCCP&M dataset. Our full-process calculation system integrates cell-level feature detection and survival analysis. During the detection phase, the CellFDet framework achieves F1 scores of 0.814, 0.819, and 0.935 for detecting polyploid giant cancer cells, mitotic figures, and general cells, respectively. In the survival analysis phase, patients were stratified into high-risk and low-risk groups based on the polyploid giant cancer cell index (P < 0.0001) and the mitotic index (P = 0.0025), with both indices demonstrating significant survival differences. Correlation analysis further confirmed these features as independent prognostic indicators for liver cancer. Our proposed system not only enables accurate detection of cell-level structural features but also provides reliable survival predictions, offering a valuable tool for improving the prognosis and treatment planning for liver cancer patients.

Indexed as

Deep LearningGiant CellsLiver NeoplasmsPolyploidyAgedAlgorithmsFemaleHumansMaleMiddle AgedMitosisMitotic IndexPrognosisSurvival AnalysisLiver cancerMitotic figuresObject detectionPolyploid giant cancer cellsSurvival analysis

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.