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Steatotic liver disease in metastatic breast cancer treated with endocrine therapy and CDK4/6 inhibitor

  • Diego Malon,
  • Consolacion Molto,
  • Shopnil Prasla,
  • Danielle Cuthbert,
  • Neha Pathak,
  • Yael Berner-Wygoda,
  • Massimo Di lorio,
  • Meredith Li,
  • Jacqueline Savill,
  • Abhenil Mittal,
  • Eitan Amir,
  • Kartik Jhaveri,
  • Michelle B. Nadler

摘要

Purpose

In early-stage breast cancer, steatotic liver disease (SLD) is associated with increased recurrence, cardiovascular events, and non-cancer death. Endocrine therapy (ET) increases the risk of SLD. The impact of cyclin-dependent kinases 4/6 inhibitors (CDK4/6i) on SLD and prognostic association in metastatic breast cancer is unknown. We characterized the presence of SLD, risk factors, and treatment outcomes of SLD in metastatic HR+/HER2− breast cancer receiving CDK4/6i.

Methods

This single institution, retrospective, cohort study included patients with metastatic HR+/HER2− breast cancer receiving first-line ET and CDK4/6i from January 2018 to June 2022. SLD was defined as a Liver Attenuation Index (LAI) > 25 HU on contrast-enhanced CT scans and/or > 10 HU on plain CT scans. Univariable binary-logistic regression was used to assess associations with SLD. Time to treatment failure (TTF) and overall survival (OS) were analyzed using Cox proportional hazards modeling.

Results

Among 87 patients with a median age of 58 years and 65.5% postmenopausal, 50 (57.5%) had SLD at anytime (24 at baseline, 26 acquired). SLD at baseline was statistically associated with post-menopausal status. It was quantitatively but not statistically associated with age > 65, diabetes, smoking, and HER2-low. SLD at anytime was statistically significantly associated with longer TTF (median 470 vs 830.5 days, HR = 0.38, p < 0.001). No significant differences in OS or grade 3/4 adverse events were observed between groups.

Conclusion

This study demonstrated a high prevalence of SLD in this population, with SLD presence correlated with longer TTF. SLD may be an indicator of better outcomes in metastatic HR+/HER2− breast cancer patients treated with CDK4/6i.