Effect of candesartan and metoprolol on myocardial tissue composition during anthracycline treatment: the PRADA trial

Eur Heart J Cardiovasc Imaging. 2018 May 1;19(5):544-552. doi: 10.1093/ehjci/jex159.

Abstract

Aims: Anthracycline treatment may cause myocyte loss and expansion of the myocardial extracellular volume (ECV) fraction by oedema and fibrosis. We tested the hypotheses that adjuvant treatment for early breast cancer with the anthracycline epirubicin is dose dependently associated with increased ECV fraction and total ECV, as well as reduced total myocardial cellular volume, and that these changes could be prevented by concomitant angiotensin or beta-adrenergic blockade.

Methods and results: PRevention of cArdiac Dysfunction during Adjuvant breast cancer therapy (PRADA) was a 2 × 2 factorial, placebo-controlled, double-blinded trial of candesartan and metoprolol. Sixty-nine women had valid ECV measurements. ECV fraction, total ECV, and total cellular volume were measured by cardiovascular magnetic resonance before and at the completion of anthracycline therapy. ECV fraction increased from 27.5 ± 2.7% to 28.6 ± 2.9% (P = 0.002). A cumulative doxorubicin equivalent dose of 268 mg/m2 was associated with greater increase in ECV fraction than doses <268 mg/m2 (mean change 3.4% [95% confidence interval (CI) 1.2, 5.5] vs. 0.7% [95% CI 0.0, 1.5], P = 0.006), as well as greater increase in total ECV (1.9 mL [95% CI 0.4, 3.5] vs. 0.1 mL [95% CI -0.6, 0.8], P = 0.04). In patients receiving candesartan, total cellular volume decreased (-3.5 mL [95% CI - 4.7, -2.2], P < 0.001) while in patients not receiving candesartan, it remained unchanged (P = 0.45; between group difference P = 0.003).

Conclusions: Anthracycline therapy is associated with dose-dependent increase in ECV fraction and total ECV. Concomitant treatment with candesartan reduces left ventricular total cellular volume.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Anthracyclines / adverse effects*
  • Anthracyclines / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Benzimidazoles / adverse effects*
  • Benzimidazoles / therapeutic use
  • Biphenyl Compounds
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology
  • Breast Neoplasms / surgery
  • Cardiotoxicity / diagnostic imaging*
  • Cardiotoxicity / mortality
  • Cardiotoxicity / physiopathology
  • Chemotherapy, Adjuvant
  • Cyclophosphamide / adverse effects
  • Cyclophosphamide / therapeutic use
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Epirubicin / adverse effects
  • Epirubicin / therapeutic use
  • Female
  • Fluorouracil / adverse effects
  • Fluorouracil / therapeutic use
  • Hospitals, University
  • Humans
  • Kaplan-Meier Estimate
  • Magnetic Resonance Imaging, Cine / methods*
  • Mastectomy / methods
  • Middle Aged
  • Norway
  • Prognosis
  • Prospective Studies
  • Risk Assessment
  • Statistics, Nonparametric
  • Stroke Volume / drug effects
  • Survival Analysis
  • Tetrazoles / adverse effects*
  • Tetrazoles / therapeutic use

Substances

  • Anthracyclines
  • Benzimidazoles
  • Biphenyl Compounds
  • Tetrazoles
  • Epirubicin
  • Cyclophosphamide
  • candesartan
  • Fluorouracil

Supplementary concepts

  • FEC protocol