Evidence map›Paper›PMID 42238067›Full record

ArticleArXiv2026

An Open Multi-Center Whole-Body FDG PET/CT Foundation Model for Tumor Segmentation.

Xiaofeng Liu, Qianru Zhang, Thibault Marin, Menghua Xia, Chi Liu, Georges El Fakhri, Jinsong Ouyang

Abstract readPreprint
In one paragraph

Article in ArXiv, 2026. 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

7 authors.

Xiaofeng LiuDepartment of Radiology and Biomedical Imaging, Yale Biomedical Imaging Institute, Yale University, New Haven, CT, USA.
Qianru ZhangDepartment of Radiology and Biomedical Imaging, Yale Biomedical Imaging Institute, Yale University, New Haven, CT, USA.
Thibault MarinDepartment of Radiology and Biomedical Imaging, Yale Biomedical Imaging Institute, Yale University, New Haven, CT, USA.
Menghua XiaDepartment of Radiology and Biomedical Imaging, Yale Biomedical Imaging Institute, Yale University, New Haven, CT, USA.
Chi LiuDepartment of Radiology and Biomedical Imaging, Yale Biomedical Imaging Institute, Yale University, New Haven, CT, USA.
Georges El FakhriDepartment of Radiology and Biomedical Imaging, Yale Biomedical Imaging Institute, Yale University, New Haven, CT, USA.
Jinsong OuyangDepartment of Radiology and Biomedical Imaging, Yale Biomedical Imaging Institute, Yale University, New Haven, CT, USA.

Funding

Unified Joint Statistical Reconstruction of PET & MRP41EB022544 · NIBIB · YALE UNIVERSITY · PI Georges El Fakhri · 2017 to 2026
$14.8M
Multi-Center Academic-Industrial Partnership for Personalized Al-Enabled High Count PETR01CA275188 · NCI · YALE UNIVERSITY · PI RAMSEY D. BADAWI, Georges El Fakhri · 2023 to 2026
$2.5M
Deep learning-based target volume delineation capturing observer variability in head and neck cancerR01CA290745 · NCI · YALE UNIVERSITY · PI Georges El Fakhri · 2024 to 2026
$1.7M
Deep Learning-Based Treatment Planning for PSMA RPTR01CA296305 · NCI · YALE UNIVERSITY · PI Georges El Fakhri · 2025 to 2026
$1.2M
Deep Learning for Individualized Treatment Effect Inference with Multimodal DepictionR21EB034911 · NIBIB · YALE UNIVERSITY · PI Xiaofeng Liu · 2024 to 2026
$653k
NCI NIH HHS R01 CA275188NCI NIH HHS R01 CA290745NCI NIH HHS R01 CA296305NIBIB NIH HHS P41 EB022544NIBIB NIH HHS R21 EB034911
6 · The paper itself

Abstract

The synergistic interpretation of anatomical information from computed tomography (CT) and metabolic information from positron emission tomography (PET) is important to oncologic imaging. However, existing deep learning methods for PET/CT remain largely task-specific, are often trained on single-center cohorts, or adopt dual-branch fusion schemes that delay cross-modal interaction and underutilize early spatial correspondence between PET and CT. To address these limitations, we present an open-source, multi-center, whole-body FDG PET/CT foundation model utilizing 4,997 harmonized scans from four public datasets. Our framework employs hierarchical UNet-shaped backbones with early channel-wise concatenation, enabling anatomical and metabolic features to interact from the first embedding layer onward. We further introduce a masked autoencoding objective based on zero-mean imputation, combined with a weighted global reconstruction loss. This design avoids non-physical intensity discontinuities at masked-region boundaries that arise from learnable mask tokens. On downstream AutoPET lesion segmentation, the proposed models demonstrate strong label efficiency: with only 10% of the labeled training data, they achieve performance comparable to models trained from scratch on the full dataset. Under extreme 5-shot linear probing, joint PET/CT pretraining also achieves higher Dice scores than separated-modality pretraining. This multi-center foundation model demonstrates label efficiency and cross-modality representation learning for PET/CT tumor segmentation. It provides a robust, open-source basis for advancing automated oncologic imaging, significantly reducing the need for large-scale manual annotations in clinical practice.

Indexed as

Deep LearningFoundation ModelMulti-CenterPET/CTTumor Segmentation

Identifiers

PMID42238067
PMCPMC13229082

What OpenQuestion holds

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LicenceCC BY
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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.