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lauren.mccullough@emory.edu

Contributed equally: MLM and AMC

LEM, MES, KG, and YL were involved in the study concept and design with LEM directing and coordinating all study aspects. LEM, JMK, and RY led immunohistochemical analyses of tissue samples. AMC, MES, UK, and RA assessed pathologic specimens. JH, JL, AMC, and LEM led the abstraction and review of clinical data. Data preparation and statistical analyses were done by MLM, AMC, YL, and JH, and all co-authors interpreted the data. MLM, AMC, and LEM wrote the manuscript, which was reviewed, revised, and improved by all authors. All authors read and approved the final manuscript.

We acknowledge the TREC Training Workshop R25CA203650 (PI: Melinda Irwin) which facilitated the development of this work.

KG reports receiving research funding from Merck, Novartis, Pfizer, and Roche for her role at Winship Cancer Institute/Emory University as site principal investigator for clinical trials and a one-time role on the advisory board to Eisai Lilly. No potential competing interests were disclosed by the other authors.

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Research Funding:

Research was supported in part by funds from the Jimmy V Foundation (V2017-005) and the Cancer Tissue and Pathology Shared Resource of Winship Cancer Institute of Emory University and NIH/NCI under award number P30CA138292. Study data were collected and managed using REDCap electronic data capture tools hosted at Emory University.

Keywords:

  • Crown-like structures
  • Breast adipose tissue
  • Obesity
  • Progression-free survival
  • Breast cancer outcome disparity

Detection of crown-like structures in breast adipose tissue and clinical outcomes among African-American and White women with breast cancer

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Journal Title:

BREAST CANCER RESEARCH

Volume:

Volume 22

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Type of Work:

Article | Final Publisher PDF

Abstract:

Background Crown-like structures in breast adipose tissue (CLS-B), composed of necrotic adipocytes encircled by macrophages, are associated with obesity and hypothesized to worsen breast cancer prognosis; however, data are sparse, particularly in multi-racial populations. Methods We assessed specimens for CLS-B from 174 African-American and 168 White women with stage I–III breast cancer treated by mastectomy. Benign breast tissue from an uninvolved quadrant was immunohistochemically stained for CD68 to determine CLS-B presence and density (per cm2 of adipose tissue). Demographic and lifestyle factors, collected via medical record review, were analyzed for associations with CLS-B using logistic regression. Multivariable Cox proportional hazards models were used to compute hazard ratios (HRs) and 95% confidence intervals (CIs) for associations between CLS-B and overall (OS) or progression-free (PFS) survival. Results Detection of any CLS-B was similar between African-American (32%) and White (29%) patients with no evidence of an association between race and CLS-B in multivariable models (OR = 0.82, 95% CI = 0.49–1.36). Detection of CLS-B was associated with obesity (OR = 4.73, 95% CI = 2.48–9.01) and age ≥ 60 years at diagnosis (OR = 1.78, 95% CI = 0.99–3.21). There was some evidence of associations with parity and current smoking status. Detection of CLS-B was not associated with OS (HR = 1.02, 95% CI = 0.55–1.87) or PFS (HR = 0.99, 95% CI = 0.59–1.67). Conclusions Our results show a strong, positive association between BMI and CLS-B in non-tumor tissue similar to previous findings. Detection of CLS-B did not vary by race and was not associated with worse OS or PFS.

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© The Author(s) 2020

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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