Mammographic Density Decline, Tamoxifen Response, and Prognosis by Molecular Characteristics of Estrogen Receptor–Positive Breast Cancer

Author:

Abubakar Mustapha1ORCID,Mullooly Maeve2ORCID,Nyante Sarah3ORCID,Pfeiffer Ruth M1ORCID,Aiello Bowles Erin J4ORCID,Cora Renata5,Bodelon Clara1ORCID,Butler Eboneé1ORCID,Butcher Donna6,Sternberg Lawrence6,Troester Melissa A7,Weinmann Sheila8,Sherman Mark9,Glass Andrew G8,Berrington de Gonzalez Amy1ORCID,Gierach Gretchen L1ORCID

Affiliation:

1. Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health , Bethesda, MD, USA

2. School of Population Health, Royal College of Surgeons in Ireland , Dublin, Ireland

3. Department of Radiology, University of North Carolina at Chapel Hill , Chapel Hill, NC, USA

4. Kaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington , Seattle, WA, USA

5. Independent Contractor, CT(ASCP), MB(ASCP) , Stamford, CT, USA

6. Molecular Histopathology Laboratory, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA

7. Department of Epidemiology, University of North Carolina at Chapel Hill , Chapel Hill, NC, USA

8. Center for Health Research, Kaiser Permanente Northwest , Portland, OR, USA

9. Mayo Clinic , Jacksonville, FL, USA

Abstract

Abstract Background Mammographic breast density (MBD) decline post-tamoxifen initiation is a favorable prognostic factor in estrogen receptor (ER)–positive breast cancer (BC) and has potential utility as a biomarker of tamoxifen response. However, the prognostic value of MBD decline may vary by molecular characteristics among ER–positive patients. Methods We investigated associations between MBD decline (≥10% vs <10%) and breast cancer–specific mortality (BCSM) among ER–positive breast cancer patients aged 36-87 years at diagnosis treated with tamoxifen at Kaiser Permanente Northwest (1990-2008). Patients who died of BC (case patients; n = 62) were compared with those who did not (control patients; n = 215) overall and by tumor molecular characteristics (immunohistochemistry [IHC]–based subtype [luminal A–like: ER–positive/progesterone receptor [PR]–positive/HER2–negative/low Ki67; luminal B–like: ER–positive and 1 or more of PR–negative, HER2–positive, high Ki67] and modified IHC [mIHC]–based recurrence score of ER/PR/Ki67). Percent MBD was measured in the unaffected breast at baseline mammogram (mean = 6 months before tamoxifen initiation) and follow-up (mean = 12 months post-tamoxifen initiation). Adjusted odds ratios (ORs) and 95% confidence intervals (CIs) were computed from logistic regression models. All statistical tests were 2-sided. Results MBD decline was statistically significantly associated with reduced risk of BCSM overall (OR = 0.38, 95% CI = 0.15 to 0.92). This association was, however, stronger among women with aggressive tumor characteristics including luminal B–like (OR = 0.17, 95% CI = 0.04 to 0.73) vs A–like (OR = 0.74, 95% CI = 0.19 to 2.92); large (OR = 0.26, 95% CI = 0.08 to 0.78) vs small (OR = 0.41, 95% CI = 0.04 to 3.79) tumors; PR–negative (OR = 0.02, 95% CI = 0.001 to 0.37) vs PR–positive (OR = 0.50, 95% CI = 0.18 to 1.40) disease; and high (OR = 0.25, 95% CI = 0.07 to 0.93) vs low (OR = 0.44, 95% CI = 0.10 to 2.09) mIHC3 score. Conclusion The findings support MBD decline as a prognostic marker of tamoxifen response among patients with aggressive ER–positive BC phenotypes, for whom understanding treatment effectiveness is critical.

Funder

Intramural Research Funds of the Division of Cancer Epidemiology and Genetics (DCEG) of the National Cancer Institute

Department of Health and Human Services, USA

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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