Evidence map›Paper›PMID 37760629›Full record

ArticleCancers2023

MRI Assessment of Changes in Tumor Vascularization during Neoadjuvant Anti-Angiogenic Treatment in Locally Advanced Breast Cancer Patients.

Torgeir Mo, Siri Helene Bertelsen Brandal, Oliver Marcel Geier, Olav Engebråten, Line Brennhaug Nilsen, Vessela N Kristensen, Knut Håkon Hole, Tord Hompland, Thomas Fleischer, Therese Seierstad

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Monitoring Pharmacological Treatment of Breast Cancer with MRI.Current issues in molecular biology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. 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

10 authors at 1 institution in 1 country.

Torgeir MoFaculty of Clinical Medicine, University of Oslo, 0316 Oslo, Norway.ORCID 0000-0001-6817-6625
Siri Helene Bertelsen BrandalFaculty of Clinical Medicine, University of Oslo, 0316 Oslo, Norway.ORCID 0000-0001-7749-4481
Oliver Marcel GeierDepartment of Diagnostic Physics, Oslo University Hospital, 0379 Oslo, Norway.ORCID 0000-0003-3919-7579
Olav EngebråtenFaculty of Clinical Medicine, University of Oslo, 0316 Oslo, Norway.
Line Brennhaug NilsenDepartment of Medical Physics, Oslo University Hospital, 0379 Oslo, Norway.
Vessela N KristensenFaculty of Clinical Medicine, University of Oslo, 0316 Oslo, Norway.
Knut Håkon HoleFaculty of Clinical Medicine, University of Oslo, 0316 Oslo, Norway.
Tord HomplandDepartment of Radiation Biology, Oslo University Hospital, 4950 Oslo, Norway.
Thomas FleischerDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, 4950 Oslo, Norway.ORCID 0000-0003-0985-8460
Therese SeierstadDepartment of Research and Development, Division for Radiology and Nuclear Medicine, Oslo University Hospital, 0379 Oslo, Norway.ORCID 0000-0002-2579-5298
Oslo University Hospital · NO

Funding

European Union's Horizon 2020 Research and Innovation Programme 847912UiO: Life Science initiative PerCaThe
6 · The paper itself

Abstract

Anti-VEGF (vascular endothelial growth factor) treatment improves response rates, but not progression-free or overall survival in advanced breast cancer. It has been suggested that subgroups of patients may benefit from this treatment; however, the effects of adding anti-VEGF treatment to a standard chemotherapy regimen in breast cancer patients are not well studied. Understanding the effects of the anti-vascular treatment on tumor vasculature may provide a selection of patients that can benefit. The aim of this study was to study the vascular effect of bevacizumab using clinical dynamic contrast-enhanced MRI (DCE-MRI). A total of 70 women were randomized to receive either chemotherapy alone or chemotherapy with bevacizumab for 25 weeks. DCE-MRI was performed at baseline and at 12 and 25 weeks, and in addition 25 of 70 patients agreed to participate in an early MRI after one week. Voxel-wise pharmacokinetic analysis was performed using semi-quantitative methods and the extended Tofts model. Vascular architecture was assessed by calculating the fractal dimension of the contrast-enhanced images. Changes during treatment were compared with baseline and between the treatment groups. There was no significant difference in tumor volume at any point; however, DCE-MRI parameters revealed differences in vascular function and vessel architecture. Adding bevacizumab to chemotherapy led to a pronounced reduction in vascular DCE-MRI parameters, indicating decreased vascularity. At 12 and 25 weeks, the difference between the treatment groups is severely reduced.

Indexed as

angiogenesis inhibitorsbreast neoplasmsfractalsmagnetic resonance imagingneoadjuvant therapypharmacokinetics

Identifiers

PMID37760629
PMCPMC10526130
OpenAlexW4386929581

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.