Evidence map›Paper›PMID 41994001›Full record

ArticleNeuro-oncology advances

Automatic longitudinal assessment of brain metastases improves detection of disease progression.

David Weiss, Khaled Bousabarah, Nazanin Maleki, Saahil Chadha, Divya Ramakrishnan, Ajay Malhotra, Ahmed W Moawad, Klara Osenberg, Spyridon Bakas, Veronica Chiang and 8 more

Abstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

David WeissDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0009-0002-2164-4780
Khaled BousabarahVisage Imaging, GmbH, Berlin, Germany.
Nazanin MalekiDepartment of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID https://orcid.org/0000-0001-5725-8027
Saahil ChadhaDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0009-0002-8519-7895
Divya RamakrishnanDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0000-0003-2581-1793
Ajay MalhotraDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0000-0001-9223-6640
Ahmed W MoawadDivision of Neuroradiology, Department of Radiology, Hospital of University of Pennsylvania, Philadelphia, PA, USA.
Klara OsenbergDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0009-0002-5062-2388
Spyridon BakasDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID https://orcid.org/0000-0001-8734-6482
Veronica ChiangDepartment of Neurosurgery, Yale School of Medicine, New Haven, CT, USA.
Wondwossen LereboDepartment of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Dirk Smeetsicometrix, Leuven, Belgium.ORCID https://orcid.org/0000-0003-1153-094X
Elizabeth SchrickelDepartment of Neuroradiology, Wexner Medical Center, Ohio State University, Columbus, OH, USA.
Fatima MemonCarolina Radiology, Myrtle Beach, SC, USA.
Sanjay AnejaDepartment of Therapeutic Radiology, Yale School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0000-0001-5681-7528
Cornelius DeuschlDepartment of Diagnostic and Interventional Radiology and Neuroradiology, Essen University Hospital, Essen, Germany.ORCID https://orcid.org/0000-0001-9262-7289
Mingde LinDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0000-0001-7641-2595
Mariam AboianDepartment of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID https://orcid.org/0000-0002-4877-8271

Funding

PET Biomarker for synaptic density changes after radiation therapyR01CA275767 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI Mariam Aboian · 2024 to 2026
$2.2M
The Federated Tumor Segmentation (FeTS) platform: An intuitive tool facilitating secure multi-institutional collaborationU01CA242871 · NCI · UNIVERSITY OF PENNSYLVANIA · PI BAKAS, SPYRIDON · 2019 to 2021
$1.1M
NCI NIH HHS R01 CA275767NCI NIH HHS U01 CA242871
6 · The paper itself

Abstract

Background: Characterization of multiple brain metastases (BMs) during treatment is limited by lack of available tools for individual volumetric lesion tracking. This study investigated role of a Picture Archiving and Communication System (PACS)-integrated artificial intelligence (AI) prototype lesion tracking tool (AI-LTT) for segmentation, enabling automatic assessment of longitudinal lesion changes compared to manual analysis by 2 neuroradiologists, focusing on inter-observer variability. Methods: Longitudinal studies of patients with BMs who underwent stereotactic radiotherapy were assessed. In manual workflow, 2 board-certified neuroradiologists displayed current and up to 7 prior studies of each patient and measured orthogonal lesion diameters (DMAX) manually. In AI-LTT-assisted workflow, a custom hanging protocol automatically selected, displayed, and 3D registered T1 gadolinium-enhanced MR sequences in up to 8 studies. A Scalable and Transferable U-Net (STU-Net) trained on BraTS METS 2023 BM dataset was used for segmentations from which DMAX were extrapolated. Neuroradiologists revised AI measurements as needed. Time and number of mouse clicks for both workflows were recorded. Results: A total of 40 patients with 158 MRIs were investigated. Median DSC of STU-Net segmentations was 0.771. Intra-class and Spearman correlation coefficients of manual diameter measurements were 0.959 and 0.961, respectively. Out of 353 true lesions, 59 were detected by only one (R1) and 15 by only the second neuroradiologist (R2). Among 74 lesions discrepant between readers, 14 proceeded to complete response, 4 partial response, 39 stable disease, but 12 developed progressive disease. Conclusions: AI-assisted workflow for BM analysis improves follow up of lesions and has potential to improve detection of lesions that progress over time of treatment.

Indexed as

artificial intelligencebrain metastasisinter-rater variabilitylesion trackingtreatment response assessment

Identifiers

PMID41994001
PMCPMC13082478

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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.