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. 2021 May 6;13(9):2222. doi: 10.3390/cancers13092222

Table 1.

Overview of the epidemiologic studies examining CLS-B and female breast cancer.

First Author (Year) Study Design Institutions/
Affiliations
Country,
Race/
Ethnicity Distribution
Study Population Study Years CLS-B Analyses Conducted
Breast cancer incidence studies (n = 2)
Shaik (2020) [84] Nested case–control + cross-sectional analysis Detroit BBD cohort and KTB USA
100% AA
n = 84 BBD cases
n = 47 BBD controls
n = 50 KTB volunteers without BBD or breast cancer
BBD diagnosis: 1997–2010
Follow up for breast cancer through 2016
  • Association between CLS-B and breast cancer among AA women with BBD

  • CLS-B occurrence in normal breast tissue

  • BMI and CLS-B associations

  • Adipocyte diameter and CLS-B

  • Associations between IL (another inflammatory marker) with breast cancer and BBD among AA women

Carter (2017) [85] Nested case–control + cross-sectional analysis Mayo BBD cohort and KTB USA
Unknown
n = 86 BBD cases
n = 86 BBD controls
n = 86 KTB volunteers without clinical breast abnormalities
BBD diagnosis: 1967–2001
Follow up for breast cancer: Unknown
  • Association between CLS-B and breast cancer among BBD patients

  • CLS-B occurrence in normal breast tissue

  • Participant and clinical characteristics associated with CLS-B

  • Stromal CD68+ macrophage infiltration by BBD and breast cancer status

Breast cancer prognosis studies (n = 4)
Maliniak (2020) [69] Cohort + cross-sectional analysis Emory University-affiliated tumor registries USA
51% AA
49% White
n = 342 breast cancer patients
  • Age ≥ 18 years old

  • Stage I–III, invasive

  • Underwent mastectomy

  • No neoadjuvant treatment

Breast cancer diagnosis: 2007–2012
Follow up for breast cancer outcomes: 2018
  • Association between CLS-B and breast cancer prognosis

  • Occurrence of CLS-B by race (AA vs. White)

  • Participant and tumor characteristics associated with CLS-B

  • Adipocyte number and CLS-B

Cha (2018) [86] Cohort + cross-sectional analysis Yonsei University South Korea Group 1: n = 56 non-breast cancer patients
  • Tissue from reduction mammoplasty

Group 2: n = 84 breast cancer patients
  • Non-tumor breast tissue

Group 3: n = 140 breast cancer patients
  • Tumor-containing breast tissue

Unknown
  • Association between CLS-B and breast cancer prognosis (Group 3 only)

  • Occurrence of CLS-B by breast cancer status and type of tissue among breast cancer patients (non-neoplastic vs. neoplastic)

  • Participant and tumor characteristics associated with CLS-B (Group 3 only)

  • Associations between number of infiltrating CD68+ and CD163+ in adipose tissue and tumor tissue with CLS-B detected by CD68 and CD163 (Group 3 only)

Koru-Sengul (2016) [87] Cohort + cross-sectional analysis University of Miami/Jackson Memorial Hospital tumor registry USA
33% Black
33% non-Black Latina
33% Caucasian
n = 150 breast cancer patients
  • Stage I–IV

  • No previous exposure to chemotherapy, radiotherapy, or hormonal therapy

Cases obtained: 1978–1997
Followed for at least 5 years
  • Association between CLS-B and breast cancer prognosis

  • Density of CLS-B across racial groups (Black, non-Black Latina, and Caucasian)

  • Differences in densities of CLS-B macrophage phenotypes (M1, M2, pan) across racial groups

  • Densities of TAMs by macrophage marker type and across racial groups

  • Proliferative capacity of TAMs by proximity to tumor cells and across racial ethnic groups

Iyengar (2016) [82] Cohort + cross-sectional analysis MSKCC USA
83% White
13% Black
3% Asian
Cohort 1: n = 100 patients (mostly breast cancer)
  • Underwent mastectomy

Cohort 2: n = 127 breast cancer patients
  • All developed distant metastases but initially diagnosed with stage I–III breast cancer

Mastectomy:
2011–2013 (Cohort 1); 2001–2006 (Cohort 2)
Cohort 2: Follow up for breast cancer outcomes: 2014
Cohort 1:
  • Participant and tumor characteristics associated with CLS-B

  • Circulating metabolic and inflammatory markers associated with CLS-B

Cohort 2:
  • Association between CLS-B and breast cancer prognosis

  • Participant and tumor characteristics associated with CLS-B

Cross-sectional studies of CLS-B (n = 8)
Greenlee (2018) [70] Cross-sectional Columbia University Medical Center USA
100% Hispanic a
n = 91 breast cancer patients
  • Stage 0–III

  • Underwent mastectomy

  • 16% had neoadjuvant chemotherapy

Mastectomy: 2007–2012
  • Occurrence of CLS-B among Hispanic/Latina breast cancer patients

  • Participant and tumor characteristics associated with CLS-B

  • Adipocyte diameter and CLS-B

  • Liver function biomarkers and CLS-B

Iyengar (2018) [81] Cross-sectional National Taiwan University Hospital and MSKCC Taiwan
USA
100% Caucasian
n = 72 Taiwanese breast cancer patients
  • Non-metastatic

  • Underwent mastectomy

  • n = 267 US Caucasian patients

  • Underwent mastectomy

Mastectomy: 2011–2016 (Taiwanese); 2011–2013 (US Caucasian)
  • Comparisons of CLS-B and breast adipocyte size in Taiwanese vs.US Caucasian women

  • Participant and tumor characteristics associated with CLS-B (Taiwanese only)

  • Body composition (body fat, VAT, SAT) factors associated with CLS-B (Taiwanese only)

  • Circulating metabolic and inflammatory markers associated with CLS-B (Taiwanese only)

  • Adipocyte diameter and CLS-B

Iyengar (2017) [71] Cross-sectional MSKCC USA
76% Caucasian
9% Black, Asian, or Other
14% Unknown
n = 72 patients (mostly breast cancer)
  • Normal weight (BMI < 25 kg/m2)

  • Underwent mastectomy

Mastectomy: 2011–2013
  • Occurrence of CLS-B in normal weight women

  • Participant and tumor characteristics associated with CLS-B

  • Circulating metabolic and inflammatory markers associated with CLS-B

  • Circulating leptin and CLS-B, aromatase expression, and adipocyte diameter associations

  • Adipocyte diameter and CLS-B

  • Aromatase activity and CLS-B, BMI, and adipocyte diameter associations

Mullooly (2017) [80] Cross-sectional PBCS Poland n = 83 breast cancer patients
  • Invasive breast cancer

  • Postmenopausal and not taking hormone replacement

  • Underwent surgery

  • No neoadjuvant treatment

Study recruitment: 2000–2003
  • Participant and tumor characteristics associated with CLS-B and number of CD68-positive cells

  • CLS-B associations with concentrations and ratios of sex-steroid hormones in breast adipose tissue vs. systemic circulation

Vaysse (2017) [83] Cross-sectional Energy Balance and Breast Cancer Aspects-II Norway n = 107 breast cancer patients
  • Aged 25–75 years

  • Stage I–II, invasive

  • 71% underwent breast conserving surgery

Unknown
  • BMI, WHR, % truncal fat and CLS-B associations overall and by menopausal status

  • Circulating metabolic and inflammatory markers associated with CLS-B overall and by menopausal status

  • Adipocyte diameter and CLS-B

Brown (2017) [72] Cross-sectional MSKCC USA n = 161 patients (mostly breast cancer)
  • Aged 27–74 years

  • Underwent mastectomy

Unknown
  • Menopause and CLS-B association

  • The effect of menopause on CLS-B and aromatase expression associations

Iyengar (2015) [73] Cross-sectional MSKCC USA
86% White
7% Black
6% Asian
n = 237 patients (mostly breast cancer)
  • Aged 22–90 years

  • Underwent mastectomy

  • 14% received preoperative chemotherapy

  • 39% of those tested had BRCA1/2 mutation

Mastectomy: 2011–2013
  • Participant and tumor characteristics associated with CLS-B

  • Adipocyte diameter and CLS-B

  • Comparison of CLS-B status between bilateral breasts

  • Comparison of CLS-B status with abdominal CLS status

Morris (2011) [67] Cross-sectional (pilot study) MSKCC USA n = 30 patients (mostly breast cancer)
  • Aged 26–70 years

  • Underwent mastectomy

Enrolled: 2010
  • BMI and CLS-B association

  • Adipocyte diameter and CLS-B

  • Aromatase expression and activity and CLS-B

  • NF-kB binding activity and CLS-B

Abbreviations: BBD = benign breast disease; BMI = body mass index; CLS-B = crown-like structures in breast adipose tissue; IL = infiltrating lymphocytes; KTB = Komen Normal Tissue Bank; MSKCC = Memorial Sloan Kettering Cancer Center; PBCS = Polish Breast Cancer Study; TAMs = tumor-associated macrophages; WHR = waist-to-hip ratio; USA = United States of America. a Greenlee et al. (2018) also included information on country of origin: 63% Dominican Republic, 16% Puerto Rican, 2% South American, 2% Mexican, and 16% Other Hispanic.