Evidence map›Paper›PMID 35406609›Full record

ArticleCancers2022

Quantifying Tumor Heterogeneity via MRI Habitats to Characterize Microenvironmental Alterations in HER2+ Breast Cancer.

Anum S Kazerouni, David A Hormuth, Tessa Davis, Meghan J Bloom, Sarah Mounho, Gibraan Rahman, John Virostko, Thomas E Yankeelov, Anna G Sorace

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Trial
  2. Utilization of MRI-based radiomics nomogram for predicting HER2-zero, -low, and -overexpression breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Multicenter study provides radiomic and biological insights into neoadjuvant chemotherapy response and prognosis in luminal breast cancer.Cancer imaging : the official publication of the International Cancer Imaging Society · 2026
    Article
  8. Article
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  13. Review
  14. Article
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  17. Review
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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

9 authors.

Anum S KazerouniDepartment of Radiology, The University of Washington, Seattle, WA 98104, USA.ORCID 0000-0002-4200-534X
David A HormuthOden Institute for Computational Engineering and Sciences, The University of Texas at Austin, Austin, TX 78712, USA.ORCID 0000-0002-9643-1694
Tessa DavisDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.
Meghan J BloomDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.
Sarah MounhoDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.
Gibraan RahmanDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.
John VirostkoLivestrong Cancer Institutes, The University of Texas at Austin, Austin, TX 78712, USA.ORCID 0000-0003-3413-8801
Thomas E YankeelovOden Institute for Computational Engineering and Sciences, The University of Texas at Austin, Austin, TX 78712, USA.ORCID 0000-0001-6201-3913
Anna G SoraceDepartment of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL 35294, USA.ORCID 0000-0002-3640-3966

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Omer Jamy · 1985 to 2026
$165.9M
INTEGRATING OMICS AND QUANTITATIVE IMAGING DATA IN CO-CLINICAL TRIALS TO PREDICT TREATMENT RESPONSE IN TRIPLE NEGATIVE BREAST CANCERU24CA226110 · NCI · BAYLOR COLLEGE OF MEDICINE · PI LEWIS, MICHAEL T., RUBIN, DANIEL L · 2019 to 2023
$3.2M
Comprehensive Training Program in Imaging Science and InformaticsT32EB007507 · NIBIB · UNIVERSITY OF TEXAS AT AUSTIN · PI MARKEY, MIA K, RYLANDER, HENRY GRADY · 2009 to 2024
$2.7M
Evaluation and Validation of Imaging Biomarkers of Tumor Response to TreatmentR01CA138599 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MCINTYRE, JAMES OLIVER · 2010 to 2015
$2.2M
Personalizing immunotherapy in HER2+ breast cancer through quantitative imagingR01CA240589 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SORACE, ANNA C · 2020 to 2023
$1.6M
American Cancer Society RSG-18-006-01-CCECancer Prevention and Research Institute of Texas RR160005NCI NIH HHS P30 CA013148NCI NIH HHS P30CA016672NIBIB NIH HHS T32 EB007507NIH HHS R01CA138599NIH HHS R01CA240589NIH HHS T32EB007507NIH HHS U01CA17470NIH HHS U24CA226110
6 · The paper itself

Abstract

This study identifies physiological habitats using quantitative magnetic resonance imaging (MRI) to elucidate intertumoral differences and characterize microenvironmental response to targeted and cytotoxic therapy. BT-474 human epidermal growth factor receptor 2 (HER2+) breast tumors were imaged before and during treatment (trastuzumab, paclitaxel) with diffusion-weighted MRI and dynamic contrast-enhanced MRI to measure tumor cellularity and vascularity, respectively. Tumors were stained for anti-CD31, anti-ɑSMA, anti-CD45, anti-F4/80, anti-pimonidazole, and H&E. MRI data was clustered to identify and label each habitat in terms of vascularity and cellularity. Pre-treatment habitat composition was used stratify tumors into two "tumor imaging phenotypes" (Type 1, Type 2). Type 1 tumors showed significantly higher percent tumor volume of the high-vascularity high-cellularity (HV-HC) habitat compared to Type 2 tumors, and significantly lower volume of low-vascularity high-cellularity (LV-HC) and low-vascularity low-cellularity (LV-LC) habitats. Tumor phenotypes showed significant differences in treatment response, in both changes in tumor volume and physiological composition. Significant positive correlations were found between histological stains and tumor habitats. These findings suggest that the differential baseline imaging phenotypes can predict response to therapy. Specifically, the Type 1 phenotype indicates increased sensitivity to targeted or cytotoxic therapy compared to Type 2 tumors.

Indexed as

BT-474diffusion-weighted MRIdynamic contrast-enhanced MRIhabitat imagingimmunofluorescenceimmunohistochemistrypaclitaxeltrastuzumab

Identifiers

PMID35406609
PMCPMC8997932

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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.