Atorvastatin and Myocardial Extracellular Volume Expansion During Anthracycline-Based Chemotherapy.

in JACC. CardioOncology by Vencel Juhasz, Thiago Quinaglia, Zsofia D Drobni, Julius C Heemelaar, Donna S Neuberg, Yuchi Han, Bonnie Ky, Raymond Y Kwong, James L Januzzi, Aarti Asnani, Robert A Redd, Negareh Mousavi, Michael Jerosch-Herold, Marielle Scherrer-Crosbie, Tomas G Neilan

TLDR

  • Atorvastatin reduced the increase in myocardial extracellular volume (ECV) and preserved left ventricular ejection fraction in patients with lymphoma treated with anthracyclines.

Abstract

In the STOP-CA (Statins to Prevent the Cardiotoxicity From Anthracyclines) trial, atorvastatin preserved the left ventricular ejection fraction among patients with lymphoma treated with anthracyclines. The protective mechanisms are currently unclear. The aim of this study was to test the effect of atorvastatin on the anthracycline-associated increase in myocardial extracellular volume (ECV) using cardiac magnetic resonance imaging (MRI). Cardiac MRI with mapping was performed at baseline and at 12-month follow-up. ECV was calculated, and the primary endpoint was a ≥3% increase. Increases of ≥1 SD in native T1 and T2 times and ECV were secondary endpoints. The subgroup included 171 participants with paired cardiac MRI scans, and 127 had contrast scans of appropriate quality (median age 52 years, 47% women). The proportion of participants with ≥3% increases in ECV was lower in the atorvastatin compared with the placebo group (8% vs 29%; P = 0.002; OR: 0.20; 95% CI: 0.06 to 0.59). A ≥3% increase in ECV was associated with an 8.4% decrease in left ventricular ejection fraction at follow-up (95% CI: -6.31 to -10.38; P < 0.001). The proportion of participants with ≥1-SD increases in T1 and T2 times was statistically similar between groups at 12 months. At 24 months, there were fewer heart failure events among those without ≥3% increases in ECV (8% vs 24%; P = 0.054), though not statistically significantly. Compared with placebo, atorvastatin limited ECV expansion among participants with lymphoma undergoing anthracycline chemotherapy. This study is the first to provide mechanistic insight into statins' cardioprotective effects with anthracyclines. (Statins to Prevent the Cardiotoxicity From Anthracyclines [STOP-CA]; NCT02943590).

Overview

  • The STOP-CA trial tested the effect of atorvastatin on preserving the left ventricular ejection fraction in patients with lymphoma treated with anthracyclines.
  • The study used cardiac magnetic resonance imaging (MRI) to measure the increase in myocardial extracellular volume (ECV) as a primary endpoint.
  • The study aimed to provide mechanistic insight into statins' cardioprotective effects with anthracyclines.

Comparative Analysis & Findings

  • Atorvastatin reduced the proportion of participants with ≥3% increases in ECV compared to the placebo group (8% vs 29%; P = 0.002).
  • A ≥3% increase in ECV was associated with an 8.4% decrease in left ventricular ejection fraction at follow-up.
  • No significant differences were found in the proportion of participants with ≥1 SD increases in T1 and T2 times between the two groups.

Implications and Future Directions

  • The study's findings suggest that atorvastatin may limit ECV expansion among patients with lymphoma undergoing anthracycline chemotherapy, potentially reducing cardiotoxicity.
  • Future studies should investigate the optimal timing and duration of statin therapy in patients receiving anthracyclines.
  • Long-term follow-up studies are necessary to evaluate the potential prevention of heart failure events and assess the durability of statins' cardioprotective effects.