Evidence map›Paper›PMID 33516237›Full record

ArticleBreast cancer research : BCR2021

Infiltrating immune cells in benign breast disease and risk of subsequent invasive breast cancer.

Thomas E Rohan, Rhonda Arthur, Yihong Wang, Sheila Weinmann, Mindy Ginsberg, Sherene Loi, Roberto Salgado

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. The Presence of Non-Exhausted Senescent T Cells in Breast Cancer Patients.Asian Pacific journal of cancer prevention : APJCP · 2025
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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

7 authors at 5 institutions in 3 countries.

Thomas E RohanDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, NY, 10461, USA. thomas.rohan@einsteinmed.org.ORCID 0000-0001-6897-4045
Rhonda ArthurDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, NY, 10461, USA.
Yihong WangDepartment of Pathology and Laboratory Medicine, Rhode Island Hospital and Lifespan Medical Center, Warren Alpert Medical School of Brown University, Providence, RI, 02903, USA.
Sheila WeinmannCenter for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
Mindy GinsbergDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, NY, 10461, USA.
Sherene LoiSir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Australia.
Roberto SalgadoDivision of Research, Peter MacCallum Cancer Centre, Melbourne, Australia.
Albert Einstein College of Medicine · USBrown University · USKaiser Permanente Center for Health Research · USPeter MacCallum Cancer Centre · AUThe University of Melbourne · AU

Funding

microRNA expression profiling of benign breast tissue and breast cancer riskR01CA142942 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI ROHAN, THOMAS E · 2010 to 2014
$3.6M
Breast Cancer Research Foundation BCRF-17-194Breast Cancer Research Foundation BCRF-18-140NCI NIH HHS R01 CA142942
6 · The paper itself

Abstract

backgroundIt is well established that tumors are antigenic and can induce an immune response by the host, entailing lymphocytic infiltration of the tumor and surrounding stroma. The extent and composition of the immune response to the tumor, assessed through evaluation of tumor-infiltrating lymphocyte counts, has been shown in many studies to have prognostic and predictive value for invasive breast cancer, but currently, there is little evidence regarding the association between infiltrating immune cell counts (IICCs) in women with benign breast disease (BBD) and risk of subsequent invasive breast cancer.

methodsUsing a cohort of 15,395 women biopsied for BBD at Kaiser Permanente Northwest, we conducted a nested case-control study in which cases were women who developed a subsequent invasive breast cancer during follow-up and controls were individually matched to cases on age at BBD diagnosis. We assessed IICCs in normal tissue and in the BBD lesions, and we used unconditional logistic regression to estimate the multivariable odds ratios (OR) and 95% confidence intervals (CI) for the associations between IICCs and breast cancer risk.

resultsThere was no association between the IICC in normal tissue (multivariable OR per 5% increase in IICC = 1.05, 95% CI = 0.96-1.16) or in the BBD lesion (OR per 5% increase in IICC = 1.06, 95% CI = 0.96-1.18) and risk of subsequent invasive breast cancer. Also, there were no associations within subgroups defined by menopausal status, BBD histology, BMI, and history of smoking.

conclusionThe results of this study suggest that IICCs in BBD tissue are not associated with altered risk of subsequent invasive breast cancer.

Indexed as

AdultBreast DiseasesBreast NeoplasmsCase-Control StudiesDisease SusceptibilityFemaleHumansMiddle AgedOdds RatioPublic Health SurveillanceRisk AssessmentRisk FactorsBenign breast diseaseBreast cancerTumor-infiltrating lymphocytes

Identifiers

PMID33516237
PMCPMC7846992
OpenAlexW3129083976

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.