Evidence map›Paper›PMID 32803155›Full record

ArticleJournal of breast imaging2020

Predictive Value of Breast MRI Background Parenchymal Enhancement for Neoadjuvant Treatment Response among HER2- Patients.

Vignesh A Arasu, Paul Kim, Wen Li, Fredrik Strand, Cody McHargue, Roy Harnish, David C Newitt, Ella F Jones, M Maria Glymour, John Kornak and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of breast imaging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
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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

13 authors at 3 institutions in 2 countries.

Vignesh A ArasuUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.ORCID 0000-0003-4315-3106
Paul KimUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.
Wen LiUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.
Fredrik StrandKarolinska University Hospital, Breast Radiology, Stockholm, Sweden.
Cody McHargueUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.
Roy HarnishUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.
David C NewittUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.
Ella F JonesUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.
M Maria GlymourUniversity of California San Francisco, Department of Epidemiology and Biostatistics, San Francisco, CA.
John KornakUniversity of California San Francisco, Department of Epidemiology and Biostatistics, San Francisco, CA.
Laura J EssermanUniversity of California San Francisco, Department of Surgery, San Francisco, CA.
Nola M HyltonUniversity of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, CA.
ISPY2 investigators
University of California, San Francisco · USKaiser Permanente · USKarolinska University Hospital · SE

Funding

The I SPY 2.2 TRIAL: Evolving to Imaging and Molecular Biomarker Response Directed Adaptive Sequential Treatment to Optimize Breast Cancer OutcomesP01CA210961 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Nola M. Hylton-Watson · 2017 to 2026
$22.9M
Real-time In Vivo MRI Biomarkers for Breast Cancer Pre-Operative Treatment TrialsR01CA132870 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HYLTON-WATSON, NOLA M., NEWITT, DAVID C · 2008 to 2019
$4.8M
Dedicated breast PET and MRI for characterization of breast cancer and its response to therapyR01CA227763 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Natsuko Onishi Yamashita · 2019 to 2026
$3.6M
Quantitative Imaging for Assessing Breast Cancer Response to TreatmentU01CA225427 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HYLTON-WATSON, NOLA M. · 2018 to 2022
$3.2M
Quantitative Imaging for Assessing Breast Cancer Response to TreatmentU01CA151235 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HYLTON-WATSON, NOLA M. · 2011 to 2015
$2.8M
NCI NIH HHS P01 CA210961NCI NIH HHS R01 CA132870NCI NIH HHS R01 CA227763NCI NIH HHS U01 CA151235NCI NIH HHS U01 CA225427
6 · The paper itself

Abstract

objectiveWomen with advanced HER2- breast cancer have limited treatment options. Breast MRI functional tumor volume (FTV) is used to predict pathologic complete response (pCR) to improve treatment efficacy. In addition to FTV, background parenchymal enhancement (BPE) may predict response and was explored for HER2- patients in the I-SPY-2 TRIAL.

methodsWomen with HER2- stage II or III breast cancer underwent prospective serial breast MRIs during four neoadjuvant chemotherapy timepoints. BPE was quantitatively calculated using whole-breast manual segmentation. Logistic regression models were systematically explored using pre-specified and optimized predictor selection based on BPE or combined with FTV.

resultsA total of 352 MRI examinations in 88 patients (29 with pCR, 59 non-pCR) were evaluated. Women with hormone receptor (HR)+HER2- cancers who achieved pCR demonstrated a significantly greater decrease in BPE from baseline to pre-surgery compared to non-pCR patients (odds ratio 0.64, 95% confidence interval (CI): 0.39-0.92,

conclusionAmong women with HER2- cancer, BPE alone demonstrated association with pCR in women with HR+HER2- breast cancer, with similar diagnostic performance to FTV. BPE predictors remained significant in multivariate FTV models, but without added discrimination for pCR prediction. This may be due to small sample size limiting ability to create subtype-specific multivariate models.

Indexed as

background parenchymal enhancementbreast cancerHER2− breast cancermagnetic resonance imagingneoadjuvant chemotherapytumor response

Identifiers

PMID32803155
PMCPMC7418876
OpenAlexW3044378295

What OpenQuestion holds

Textmetadata
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.