Pituitary & hypothalamus

Co-secretion of growth hormone and prolactin defines a high-risk acromegaly phenotype

PituitaryPublished Retrospective cohort study

Authors' conclusion

GH/PRL-PitNETs demonstrated greater tumor burden and more pronounced structural invasiveness, resulting in a significantly lower likelihood of endocrinological remission.

Study context

Population
Patients with acromegaly who underwent surgery between 2018 and 2024
Participants
188 patients
Exposure
GH/PRL-PitNETs vs GH-PitNETs
  • GH/PRL-PitNETsn = 46
  • GH-PitNETsn = 142reference
Outcome
Biochemical remission

Main finding

As reported in the abstract

Surgical remission rate
  • Surgical remission rate lower in GH/PRL-PitNETs
  • GH/PRL-PitNETs vs GH-PitNETs: P = 0.023

Observational data: associations, not effects.

Further findings

Tumor size and invasiveness

GH/PRL-PitNETs significantly larger and more invasive than GH-PitNETs

Predictors of biochemical remission (multivariable Cox analysis)

Tumor size and cavernous sinus invasion independently predicted inferior biochemical remission

Medical comorbidities

Higher incidence of comorbidities such as hypertension and thyroid carcinoma in GH-PitNETs

Original publication

Co-secretion of growth hormone and prolactin defines a high-risk acromegaly phenotype. Pituitary. Published 18 June 2026. doi:10.1007/s11102-026-01713-6

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