Evidence map›Paper›PMID 39256746›Full record

ArticleBMC medicine2024

A deep learning model for differentiating paediatric intracranial germ cell tumour subtypes and predicting survival with MRI: a multicentre prospective study.

Yanong Li, Zhizheng Zhuo, Jinyuan Weng, Sven Haller, Harrison X Bai, Bo Li, Xing Liu, Mingwang Zhu, Zheng Wang, Jane Li and 2 more

Abstract readMulticenter Study
In one paragraph

Article in BMC medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

12 authors.

Yanong Li *Department of Radiation Oncology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
Zhizheng Zhuo *Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
Jinyuan WengDepartment of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
Sven HallerUCL Institutes of Neurology and Healthcare Engineering, London, WC1E 6BT, UK.
Harrison X BaiDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Bo LiDepartment of Radiation Oncology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
Xing LiuDepartment of Neuropathology, Beijing Neurosurgery Institute, Beijing, 100070, China.
Mingwang ZhuDepartment of Radiology, Beijing Sanbo Hospital, Capital Medical University, Beijing, 100093, China.
Zheng WangDepartment of Radiation Oncology, Tianjin Huanhu Hospital, Tianjin Medical University, Tianjin, 300350, China.
Jane LiDepartment of Radiology, New York Presbyterian, Lower Manhattan Hospital, New York, NY, 10038, USA.
Xiaoguang QiuDepartment of Radiation Oncology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China. qiuxiaoguang@bjtth.org.
Yaou LiuDepartment of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China. liuyaou@bjtth.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe pretherapeutic differentiation of subtypes of primary intracranial germ cell tumours (iGCTs), including germinomas (GEs) and nongerminomatous germ cell tumours (NGGCTs), is essential for clinical practice because of distinct treatment strategies and prognostic profiles of these diseases. This study aimed to develop a deep learning model, iGNet, to assist in the differentiation and prognostication of iGCT subtypes by employing pretherapeutic MR T2-weighted imaging.

methodsThe iGNet model, which is based on the nnUNet architecture, was developed using a retrospective dataset of 280 pathologically confirmed iGCT patients. The training dataset included 83 GEs and 117 NGGCTs, while the retrospective internal test dataset included 31 GEs and 49 NGGCTs. The model's diagnostic performance was then assessed with the area under the receiver operating characteristic curve (AUC) in a prospective internal dataset (n = 22) and two external datasets (n = 22 and 20). Next, we compared the diagnostic performance of six neuroradiologists with or without the assistance of iGNet. Finally, the predictive ability of the output of iGNet for progression-free and overall survival was assessed and compared to that of the pathological diagnosis.

resultsiGNet achieved high diagnostic performance, with AUCs between 0.869 and 0.950 across the four test datasets. With the assistance of iGNet, the six neuroradiologists' diagnostic AUCs (averages of the four test datasets) increased by 9.22% to 17.90%. There was no significant difference between the output of iGNet and the results of pathological diagnosis in predicting progression-free and overall survival (P = .889).

conclusionsBy leveraging pretherapeutic MR imaging data, iGNet accurately differentiates iGCT subtypes, facilitating prognostic evaluation and increasing the potential for tailored treatment.

Indexed as

Brain NeoplasmsDeep LearningMagnetic Resonance ImagingNeoplasms, Germ Cell and EmbryonalAdolescentChildChild, PreschoolFemaleHumansMalePrognosisProspective StudiesRetrospective StudiesSurvival AnalysisDeep learning (DL)Diagnostic modelMagnetic resonance imaging (MRI)Primary intracranial germ cell tumours (iGCTs)Prognostic evaluation

Identifiers

PMID39256746
PMCPMC11389594

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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.