Evidence map›Paper›PMID 41522061›Full record

ArticleQuantitative imaging in medicine and surgery2026

Multimodality and temporal analysis of cervical cancer treatment response.

Haotian Feng, Emi Yoshida, Ke Sheng

Abstract read
In one paragraph

Article in Quantitative imaging in medicine and surgery, 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

3 authors.

Haotian FengDepartment of Radiation Oncology, University of California-San Francisco, San Francisco, CA, USA.ORCID https://orcid.org/0000-0002-0012-4594
Emi YoshidaDepartment of Radiation Oncology, University of California-San Francisco, San Francisco, CA, USA.
Ke ShengDepartment of Radiation Oncology, University of California-San Francisco, San Francisco, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cervical cancer remains a significant global health challenge, requiring improved diagnostic and prognostic tools to enhance treatment planning and outcomes. Noninvasive medical imaging offers a promising route for precision diagnostics. This study aimed to develop and evaluate a predictive model for cervical cancer treatment response during radiation therapy using features extracted from multimodal medical imaging. Methods: This study evaluated the use of multimodal medical imaging, including apparent diffusion coefficient (ADC), dynamic contrast-enhanced (DCE), and positron emission tomography (PET), across different treatment stages (pre-, mid-, and post-stage) in 22 patients with cervical cancer. From these images, we extracted and assessed the predictive performance of various feature types, including zero-order, first-order, second-order, and higher-order features. Results: Texture features, particularly those derived from the Gray Level Co-occurrence Matrix (GLCM) in two-dimensional (2D) plane, were more effective compared to other image features, achieving an area under the curve (AUC) of 0.73±0.12. Combining GLCM with shape features further increased the AUC to 0.75. Among the GLCM features, "contrast" was identified as the most predictive for treatment response (AUC of 0.74 for the top five contrast features). Among single-modality analyses, ADC demonstrated the best prediction compared to PET/computed tomography (CT) (15% AUC increase) and DCE (12% AUC increase). The combination of imaging modalities and texture analysis further enhanced patient stratification, yielding an average 8% AUC increase compared to single-modality models. Using only post-stage GLCM2D features resulted in an AUC only 4% lower than using all time points, suggesting that reduced imaging time points and modalities may still retain strong predictive power. Conclusions: Integrating texture features from multimodal imaging can improve cervical cancer prognostication and guide personalized treatment strategies. These findings support the potential of imaging biomarkers in optimizing therapy and reducing the diagnostic burden, contributing to more efficient and tailored cancer care.

Indexed as

Cervical cancerfeature extractionfeature selectionmultimodality analysistemporal analysis

Identifiers

PMID41522061
PMCPMC12780728

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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.