Evidence map›Paper›PMID 42807957›Full record

ArticleEuropean journal of radiology artificial intelligence2026

A two-stage foundation model for bladder tumor segmentation: An international multi-site study

Muhammad Awais, Oguz Akin, Giorgio Brembilla, Noah Frydenlund, Stephanie Chahwan, Josip Nincevic, Chiara Mercinelli, Antonio Cigliola, Brigida Maiorano, Francesco De Cobelli and 7 more

Abstract read
In one paragraph

Article in European journal of radiology artificial intelligence, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Muhammad AwaisDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, USA.
Oguz AkinDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA.
Giorgio BrembillaDepartment of Radiology, IRCCS San Raffaele Hospital, Comprehensive Cancer Center, Milan, Italy.
Noah FrydenlundDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, USA.
Stephanie ChahwanDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA.
Josip NincevicDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA.
Chiara MercinelliDepartment of Medical Oncology, IRCCS San Raffaele Hospital, Comprehensive Cancer Center, Milan, Italy.
Antonio CigliolaDepartment of Medical Oncology, IRCCS San Raffaele Hospital, Comprehensive Cancer Center, Milan, Italy.
Brigida MaioranoDepartment of Medical Oncology, IRCCS San Raffaele Hospital, Comprehensive Cancer Center, Milan, Italy.
Francesco De CobelliDepartment of Radiology, IRCCS San Raffaele Hospital, Comprehensive Cancer Center, Milan, Italy.
Ramesh PaudyalDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, USA.
Hikmat Al-AhmadieDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, USA.
Jonathan RosenbergDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA.
Alvin C GohDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, USA.
Andrea NecchiDepartment of Radiology, IRCCS San Raffaele Hospital, Comprehensive Cancer Center, Milan, Italy.
Lawrence H SchwartzDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, USA.
Amita Shukla-DaveDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, USA.ORCID 0000-0001-7456-3197

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Background and objective: Accurate bladder tumor segmentation is crucial for muscle invasion assessment, neoadjuvant therapy response evaluation, and bladder preservation decision-making. Manual delineation is time-consuming and observer-dependent, highlighting an unmet clinical need for accurate and automated segmentation, particularly in large multi-site studies. This study aims to (i) develop an automated MRI-based foundation model for bladder tumor segmentation (BLA-T-Seg) using a two-stage framework, in which segmentation is first constrained to the bladder wall, including wall-contiguous tumors and then refined in a second stage focused specifically on the tumor, and (ii) rigorously assess generalizability via multi-site, independent external validation across diverse cohorts. Methods: This retrospective study included T2-weighted MRI scans from 236 patients with bladder cancer across two international sites. Experienced radiologists manually annotated bladder and tumor regions of interest on T2-weighted images, which served as the ground truth. BLA-T-Seg was developed by adapting the Segment Anything Model (SAM), fine-tuned to segment the bladder in stage 1 and the tumor in stage 2. The primary performance metric was the Dice similarity coefficient (DSC), evaluated across five studies (S1-S3: internal; S4-S5: external) and benchmarked against 10 state-of-the-art (SOTA) segmentation architectures. Results: For stage 1, BLA-T-Seg achieved good-to-excellent performance, with mean DSC values ranging from 0.85 to 0.93. For stage 2, BLA-T-Seg demonstrated moderate-to-good performance, with mean DSC values of 0.74-0.81. Cross-site validation showed minimal performance variation (≤0.01-0.04), confirmed by radar plot analyses. Compared with SOTA models on subset S1, BLA-T-Seg achieved the highest DSC of 0.84, outperforming the next best-performing model, Swin Transformer (DSC: 0.56). Conclusion: BLA-T-Seg enables accurate and generalizable bladder wall and tumor segmentation and outperforms SOTA alternatives.

Indexed as

BladderMagnetic Resonance ImagingSegment Anything ModelSegmentationTumor

Identifiers

PMID42807957
PMCPMC13618362

What Socratic holds

Textmetadata
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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 Socratic graph.