Evidence map›Paper›PMID 32330067›Full record

ArticleJCO clinical cancer informatics2020

Multiresolution Application of Artificial Intelligence in Digital Pathology for Prediction of Positive Lymph Nodes From Primary Tumors in Bladder Cancer.

Stephanie A Harmon, Thomas H Sanford, G Thomas Brown, Chris Yang, Sherif Mehralivand, Joseph M Jacob, Vladimir A Valera, Joanna H Shih, Piyush K Agarwal, Peter L Choyke and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in JCO clinical cancer informatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% of its field
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

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  7. Bladder Cancer and Artificial Intelligence: Emerging Applications.The Urologic clinics of North America · 2024
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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

11 authors at 3 institutions in 1 country.

Stephanie A HarmonMolecular Imaging Branch, National Cancer Institute, Bethesda, MD.
Thomas H SanfordClinical Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD.
G Thomas BrownClinical Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD.
Chris YangMolecular Imaging Branch, National Cancer Institute, Bethesda, MD.
Sherif MehralivandMolecular Imaging Branch, National Cancer Institute, Bethesda, MD.
Joseph M JacobDepartment of Urology, Upstate Medical University, Syracuse, NY.
Vladimir A ValeraUrologic Oncology Branch, National Cancer Institute, Bethesda, MD.
Joanna H ShihDivision of Cancer Treatment and Diagnosis, Biometric Research Program, National Cancer Institute, Bethesda, MD.
Piyush K AgarwalUrologic Oncology Branch, National Cancer Institute, Bethesda, MD.
Peter L ChoykeMolecular Imaging Branch, National Cancer Institute, Bethesda, MD.
Baris TurkbeyMolecular Imaging Branch, National Cancer Institute, Bethesda, MD.
National Cancer Institute · USFrederick National Laboratory for Cancer Research · USSUNY Upstate Medical University · US

Funding

Prostate Cancer ImagingZIABC010655 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHOYKE, PETER L · 2009 to 2025
$49.2M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

purposeTo develop an artificial intelligence (AI)-based model for identifying patients with lymph node (LN) metastasis based on digital evaluation of primary tumors and train the model using cystectomy specimens available from The Cancer Genome Atlas (TCGA) Project; patients from our institution were included for validation of the leave-out test cohort.

methodsIn all, 307 patients were identified for inclusion in the study (TCGA, n = 294; in-house, n = 13). Deep learning models were trained from image patches at 2.5×, 5×, 10×, and 20× magnifications, and spatially resolved prediction maps were combined with microenvironment (lymphocyte infiltration) features to derive a final patient-level AI score (probability of LN metastasis). Training and validation included 219 patients (training, n = 146; validation, n = 73); 89 patients (TCGA, n = 75; in-house, n = 13) were reserved as an independent testing set. Multivariable logistic regression models for predicting LN status based on clinicopathologic features alone and a combined model with AI score were fit to training and validation sets.

resultsSeveral patients were determined to have positive LN metastasis in TCGA (n = 105; 35.7%) and in-house (n = 3; 23.1%) cohorts. A clinicopathologic model that considered using factors such as age, T stage, and lymphovascular invasion demonstrated an area under the curve (AUC) of 0.755 (95% CI, 0.680 to 0.831) in the training and validation cohorts compared with the cross validation of the AI score (likelihood of positive LNs), which achieved an AUC of 0.866 (95% CI, 0.812 to 0.920;

conclusionPatients who are at higher risk of having positive LNs during cystectomy can be identified on primary tumor samples using novel AI-based methodologies applied to digital hematoxylin and eosin-stained slides.

Indexed as

Urinary Bladder NeoplasmsArtificial IntelligenceHumansLymphatic MetastasisLymph NodesRetrospective StudiesTumor Microenvironment

Identifiers

PMID32330067
PMCPMC7259877
OpenAlexW3018428662

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.