Elevated risk thresholds predict endocrine risk-reducing medication use in the Athena screening registry. Academic Article uri icon

Overview

abstract

  • Risk-reducing endocrine therapy use, though the benefit is validated, is extremely low. The FDA has approved tamoxifen and raloxifene for a 5-year Breast Cancer Risk Assessment Tool (BCRAT) risk ≥ 1.67%. We examined the threshold at which high-risk women are likely to be using endocrine risk-reducing therapies among Athena Breast Health Network participants from 2011-2018. We identified high-risk women by a 5-year BCRAT risk ≥ 1.67% and those in the top 10% and 2.5% risk thresholds by age. We estimated the odds ratio (OR) of current medication use based on these thresholds using logistic regression. One thousand two hundred and one (1.2%) of 104,223 total participants used medication. Of the 33,082 participants with 5-year BCRAT risk ≥ 1.67%, 772 (2.3%) used medication. Of 2445 in the top 2.5% threshold, 209 (8.6%) used medication. Participants whose 5-year risk exceeded 1.67% were more likely to use medication than those whose risk was below this threshold, OR 3.94 (95% CI = 3.50-4.43). The top 2.5% was most strongly associated with medication usage, OR 9.50 (8.13-11.09) compared to the bottom 97.5%. Women exceeding a 5-year BCRAT ≥ 1.67% had modest medication use. We demonstrate that women in the top 2.5% have higher odds of medication use than those in the bottom 97.5% and compared to a risk of 1.67%. The top 2.5% threshold would more effectively target medication use and is being tested prospectively in a randomized control clinical trial.

authors

  • Huilgol, Yash S
  • Keane, Holly
  • Shieh, Yiwey
  • Hiatt, Robert A
  • Tice, Jeffrey A
  • Madlensky, Lisa
  • Sabacan, Leah
  • Fiscalini, Allison Stover
  • Ziv, Elad
  • Acerbi, Irene
  • Che, Mandy
  • Anton-Culver, Hoda
  • Borowsky, Alexander D
  • Hunt, Sharon
  • Naeim, Arash
  • Parker, Barbara A
  • van 't Veer, Laura J
  • Esserman, Laura J

publication date

  • August 3, 2021

Identity

PubMed Central ID

  • PMC8333106

Scopus Document Identifier

  • 85112486783

Digital Object Identifier (DOI)

  • 10.1038/s41523-021-00306-9

PubMed ID

  • 34344894

Additional Document Info

volume

  • 7

issue

  • 1