Evidence map›Paper›PMID 42151221›Full record

ArticleScientific reports2026

Diverse image generation with diffusion models and cross class label learning for polyp classification.

Vanshali Sharma, Debesh Jha, M K Bhuyan, Pradip K Das, Ulas Bagci

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
  2. Review
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

5 authors.

Vanshali SharmaDepartment of Computer Science & Engineering, Indian Institute of Technology Guwahati, Guwahati, 781039, India. vanshalisharma@alumni.iitg.ac.in.
Debesh JhaDepartment of Computer Science, University of South Dakota, Vermillion, 57069, USA.
M K BhuyanDepartment of Electronics & Electrical Engineering, Indian Institute of Technology Guwahati, Guwahati, 781039, India.
Pradip K DasDepartment of Computer Science & Engineering, Indian Institute of Technology Guwahati, Guwahati, 781039, India.
Ulas BagciMachine & Hybrid Intelligence Lab, Department of Radiology, Northwestern University, Chicago, 60611, USA.

Funding

Data Coordinating Center for the Type 1 Diabetes in Acute Pancreatitis ConsortiumU01DK127384 · NIDDK · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Vernon M Chinchilli, Temel Tirkes · 2020 to 2026
$21.3M
Cyst-X: Interpretable Deep Learning Based Risk Stratification of Pancreatic Cystic TumorsR01CA246704 · NCI · UNIVERSITY OF CENTRAL FLORIDA · PI BAGCI, ULAS · 2020 to 2024
$2.4M
Predicting Post-Covid Pulmonary Fibrosis with Explainable Deep Learning and Optimal Biomarker DiscoveryR01HL171376 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Ulas Bagci, Sachin Jambawalikar · 2024 to 2026
$2.1M
Radiologist-Centered Artificial Intelligence (RCAI) for Lung Cancer Screening and DiagnosisR01CA240639 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BAGCI, ULAS · 2020 to 2024
$2.0M
Hybrid Intelligence for Trustable Diagnosis And Patient Management of Prostate Cancer (HIT-PIRADS)U01CA268808 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Ulas Bagci · 2023 to 2026
$1.5M
DST INSPIRE IF190362NCI NIH HHS R01 CA240639NCI NIH HHS R01 CA246704NCI NIH HHS U01 CA268808NHLBI NIH HHS R01 HL171376NIDDK NIH HHS U01 DK127384NIH HHS R01-CA246704, R01-CA240639, U01 DK127384-02S1, and U01-CA268808
6 · The paper itself

Abstract

Pathologic diagnosis is a critical phase in deciding the optimal treatment procedure for dealing with colorectal cancer (CRC). Colonic polyps, precursors to CRC, can pathologically be classified into two major types: adenomatous (malignant potential) and hyperplastic (benign). Various imaging techniques, such as narrow band imaging (NBI) and white light imaging (WLI), are adopted in capturing polyp-specific features for accurate classification and have different advantages. However, the existing classification techniques mainly rely on a single imaging modality and show limited performance due to data scarcity. Recently, generative artificial intelligence has been gaining prominence in overcoming such issues, especially with various generation-controlling mechanisms using text prompts and images. However, such mechanisms require class labels to make the model respond efficiently to the provided control input. In the colonoscopy domain, such controlling mechanisms are rarely explored; specifically, the text prompt is a completely uninvestigated area. Moreover, the unavailability of expensive class-wise labels for diverse sets of images limits such explorations. This raises the key question of how diverse and clinically meaningful colonoscopy images can be generated in a text-controlled manner from limited annotated data. Therefore, in this work, we develop a novel model, PathoPolyp-Diff, that generates text-controlled synthetic images with diverse characteristics in terms of pathology, imaging modalities, and quality, enabling more effective augmentation of downstream diagnostic models. The proposed model follows a two-stage process: first, the model learns to distinguish polyp from non-polyp characteristics, and then it focuses on pathology-specific features. In the process, we introduce cross-class label learning to make the model learn features from other classes, reducing the burdensome task of data annotation. We validate the effectiveness of text-controlled synthesis and cross-class label learning by performing polyp classification (adenomatous/hyperplastic) with different imaging modalities (NBI/WLI) and text prompts. The experimental results show that incorporating the proposed synthetic images for data augmentation yields an improvement of up to 7.91% in balanced accuracy on a publicly available dataset, highlighting the utility of our approach for enhancing downstream classification performance. Moreover, cross-class label learning achieves a statistically significant improvement of up to 18.33% in balanced accuracy during video-level analysis. The code is available at https://github.com/Vanshali/PathoPolyp-Diff .

Indexed as

Colonic PolypsColorectal NeoplasmsImage Processing, Computer-AssistedClassification AlgorithmsColonoscopyGenerative Artificial IntelligenceHumansMachine Learning

Identifiers

PMID42151221
PMCPMC13376762

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.