Heart failure & cardiomyopathiesCohort study

Contemporary real-world treatment of cardiac transthyretin amyloidosis with tafamidis: a long-term multicentre study

ESC Heart FailPublished

  • retrospective, multicentre study
  • propensity-score matching for age, New York Heart Association (NYHA) class, National Amyloidosis Centre (NAC) stage, and serum albumin

Authors' conclusion

This study provides long-term real-world outcome data for ATTR-CM patients treated with tafamidis based on physician clinical judgement. Adverse outcomes were strongly predicted by low serum albumin, advanced NAC stage, and older age, emphasizing the importance of early diagnosis and timely therapy of ATTR-CM.

Study context

Population
ATTR-CM patients enrolled after commercial availability of tafamidis 61 mg in Germany (April 2020 to March 2021), with treatment initiation based on physician clinical judgementmedian age 80 [76–83] years, 85% male and 8% variant ATTR, 80% received tafamidis
Participants
329 patients
Exposure
tafamidis vs no tafamidis
Outcome
All-cause mortality
Follow-up
Median 39 [18-48] months

Main finding

As reported in the abstract

Hazard ratio

0.28

95% CI 0.13–0.61

P = 0.001

tafamidis vs no tafamidis
HR 0.28 (95% CI 0.13–0.61); P = 0.001
Patients who died (whole cohort)
21%
3-year survival, tafamidis-treated patients
86%

Observational data: associations, not effects.

Secondary outcomes

OutcomeHR (95% CI)P value
Composite of all-cause mortality and/or HF hospitalization (secondary endpoint) · median follow-up 39 [18-48] months0.56 (0.33–0.97)P = 0.039
Composite of all-cause mortality and/or heart failure (HF) hospitalization (secondary endpoint) — Patients reaching the composite endpoint (whole cohort)
42%
Composite of all-cause mortality and/or HF hospitalization (secondary endpoint) — 3-year event-free survival, tafamidis-treated patients
63%
  • Composite of all-cause mortality and/or HF hospitalization (secondary endpoint): fewer composite events with tafamidis; after propensity-score matching

Predictors of primary and secondary endpoints in tafamidis-treated patients

advanced NAC stage (primary; secondary)
P < 0.031; P < .009
age ≥80 years (primary; secondary)
P = 0.022; P = .004
serum albumin ≤42.5 g/L (primary; secondary)
P = 0.015; P < .001
NYHA class ≥III predicted only the composite endpoint (primary; secondary)
P = 0.059; P < .001

Original publication

Contemporary real-world treatment of cardiac transthyretin amyloidosis with tafamidis: a long-term multicentre study. ESC Heart Fail. Published 30 July 2026. doi:10.1093/eschf/xvag211

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