Pituitary & hypothalamus

Time to first remission and survival in patients with acromegaly: Evidence from the UK Acromegaly Register Study (UKAR)

Clin Endocrinol (Oxf)Published Cross-sectional study

Authors' conclusion

In conclusion, this population-based study conducted in patients with acromegaly revealed that faster remission time, surgical intervention and treatment with SMA are linked to improved survival outcomes.

Study context

Population
Individuals with acromegaly in the UK Acromegaly Register; median age at diagnosis 47.3 (36.5–57.8) years, 48% females, 61% white
Participants
3,569 individuals
Exposure
Time to first remission and survival
Outcome
Effect of time to remission (GH controlled at ≤2 μg/L) on survival
Methodological detailsregistry-based, accelerated failure time model
  • Registry-based
  • Accelerated failure time model

Main finding

As reported in the abstract

Survival by time to first remission
Time to first remission had a significant effect on survival
p < .001
Survival change per 1-year increase in time to first remission
median 1% reduction

Observational data: associations, not effects.

Further findings

OutcomeEstimateP value
Survival by treatmentSurgery vs No surgery · higher with surgery · adjusted for covariatessurvival rate higher 52%P < 0.001
Survival by treatmentSMA vs Dopamine agonists · higher with SMA · adjusted for covariatessurvival rate higher 18%P = 0.01
Survival by treatmentConventional radiotherapy vs No radiotherapy · lower with radiotherapy · adjusted for covariatessurvival rate lower 21%P < 0.001

First remission

Individuals with first remission
2472
Median time to first remission
1.92 (0.70-6.58) years

Original publication

Time to first remission and survival in patients with acromegaly: Evidence from the UK Acromegaly Register Study (UKAR). Clin Endocrinol (Oxf). Published 16 July 2024. doi:10.1111/cen.15112

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