Evidence map›Paper›PMID 39962614›Full record

ArticleBreast cancer research : BCR2025

Ultrasound-based quantitative microvasculature imaging for early prediction of response to neoadjuvant chemotherapy in patients with breast cancer.

Soroosh Sabeti, Nicholas B Larson, Judy C Boughey, Daniela L Stan, Malvika H Solanki, Robert T Fazzio, Mostafa Fatemi, Azra Alizad

Abstract read
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Article in Breast cancer research : BCR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Soroosh SabetiDepartment of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA.
Nicholas B LarsonDepartment of Quantitative Health Sciences, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA.
Judy C BougheyDivision of Breast and Melanoma Surgical Oncology, Department of Surgery, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA.
Daniela L StanDepartment of Medicine, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA.
Malvika H SolankiDepartment of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA.
Robert T FazzioDepartment of Radiology, Mayo Clinic College of Medicine and Science, 200 1st Street SW, Rochester, MN, 55905, USA.
Mostafa FatemiDepartment of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA.
Azra AlizadDepartment of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA. Alizad.Azra@mayo.edu.

Funding

Using Label-free Ultrasound Angio-Morphometry Analysis for Improving Ultrasound Specificity in Breast Cancer Detection and Treatment MonitoringR01CA239548 · NCI · MAYO CLINIC ROCHESTER · PI ALIZAD, AZRA, FATEMI, MOSTAFA · 2019 to 2023
$2.9M
A Contrast-free Ultrasound-based Quantitative Angio Flow Imaging Technique to Assess Peripheral Arterial Disease of Lower LimbR01HL174785 · NHLBI · MAYO CLINIC ROCHESTER · PI Azra Alizad, MOSTAFA FATEMI · 2024 to 2026
$2.1M
NCI NIH HHS R01 CA239548NHLBI NIH HHS R01 HL174785NIH HHS R01 HL174785
6 · The paper itself

Abstract

backgroundAngiogenic activity of cancerous breast tumors can be impacted by neoadjuvant chemotherapy (NAC), thus potentially serving as a marker for response monitoring. While different imaging modalities can aid in evaluation of tumoral vascular changes, ultrasound-based approaches are particularly suitable for clinical use due to their availability and noninvasiveness. In this paper, we make use of quantitative high-definition microvasculature imaging (qHDMI) based on contrast-free ultrasound for assessment of NAC response in breast cancer patients.

methodsPatients with invasive breast cancer recommended treatment with NAC were included in the study and ultrafast ultrasound data were acquired at pre-NAC, mid-NAC, and post-NAC time points. Data acquisitions also took place at two additional timepoints - at two and four weeks after NAC initiation in a subset of patients. Ultrasound data frames were processed within the qHDMI framework to visualize the microvasculature in and around the breast tumors. Morphological analyses on the microvasculature structure were performed to obtain 12 qHDMI biomarkers. Pathology from surgery classified response using residual cancer burden (RCB) and was used to designate patients as responders (RCB 0/I) and non-responders (RCB II/III). Distributions of imaging biomarkers across the two groups were analyzed using Wilcoxon rank-sum test. The trajectories of biomarker values over time were investigated and linear mixed effects models were used to evaluate interactions between time and group for each biomarker.

resultsOf the 53 patients included in the study, 32 (60%) were responders based on their RCB status. The results of linear mixed effects model analysis showed statistically significant interactions between group and time in six out of the 12 qHDMI biomarkers, indicating differences in trends of microvascular morphological features by responder status. In particular, vessel density (p-value: 0.023), maximum tortuosity (p-value: 0.049), maximum diameter (p-value: 0.002), fractal dimension (p-value: 0.002), mean Murray's deviation (p-value: 0.034), and maximum Murray's deviation (p-value: 0.022) exhibited significantly different trends based on responder status.

conclusionsWe observed microvasculature changes in response to NAC in breast cancer patients using qHDMI as an objective and quantitative contrast-free ultrasound framework. These finding suggest qHDMI may be effective in identifying early response to NAC.

Indexed as

Breast NeoplasmsMicrovesselsUltrasonography, MammaryAdultAgedFemaleHumansMiddle AgedNeoadjuvant TherapyNeovascularization, PathologicPrognosisTreatment OutcomeBreast cancerNeoadjuvant chemotherapyQuantitative high-definition microvasculature imagingUltrasound

Identifiers

PMID39962614
PMCPMC11834208

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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.