Randomised controlled trial

Sacubitril-Valsartan for the Prevention of Anthracycline Cardiotoxicity in Patients With Elevated Cardiac Troponin I Concentration During Chemotherapy: A Double-Blind Randomized Placebo-Controlled Clinical Trial: The SARAH Trial

CirculationPublished

  • Randomised controlled trial
  • double-blind
  • placebo-controlled
  • pilot

Authors' conclusion

The SARAH trial (Sacubitril-Valsartan for the Prevention of Anthracycline Cardiotoxicity in Patients With Elevated hs-cTnI Concentrations During Chemotherapy) demonstrated the potential of sacubitril-valsartan therapy to reduce the incidence of left ventricular dysfunction, as assessed by global longitudinal strain, in patients with elevated high-sensitivity cardiac troponin I after anthracycline treatment.

Study context

Population
Patients with elevated cardiac troponin I during anthracycline chemotherapy (90% women, 80.7% breast cancer)
Participants
114 patients
Comparison
Sacubitril-valsartan vs placebo
Primary endpoint
>15% reduction in global longitudinal strain from baseline
Follow-up
6 months

Primary result

As reported in the abstract

Odds ratio

0.23

95% CI 0.07–0.75

P = 0.015

Events by treatment group

Sacubitril-valsartan vs Placebo
OR 0.23 (95% CI 0.07–0.75); P = 0.015

Secondary outcomes

OutcomeP value
Change in global longitudinal strainP < 0.001

Change in global longitudinal strain

Sacubitril-valsartan: 2.5% improvement; placebo: 7.6% decline

Changes in cardiac troponin I and NT-proBNP

No significant differences

Safety

events

OutcomeSacubitril-valsartanPlaceboP value
Hypotension (SBP <100 mm Hg)81P = 0.032

Original publication

Sacubitril-Valsartan for the Prevention of Anthracycline Cardiotoxicity in Patients With Elevated Cardiac Troponin I Concentration During Chemotherapy: A Double-Blind Randomized Placebo-Controlled Clinical Trial: The SARAH Trial. Circulation. Published 13 November 2025. doi:10.1161/circulationaha.125.073322

Summarised from the published abstract; every number is checked against it