Pituitary & hypothalamus

Pasireotide as first line medical therapy for selected patients with acromegaly

PituitaryPublished Case series

Authors' conclusion

This series supports the use of pasireotide for rapid tumour control and GH reduction, in selected patients with complex and large tumours, likely to be resistant to first-generation SRLs. This approach expands the therapeutic options for managing the most challenging cases enhancing the potential for other subsequent treatment modalities.

Study context

Population
Patients with acromegaly anticipated to be resistant to first-generation somatostatin receptor ligands (SRLs): large, hyperintense tumours on T2-weighted MRI and sparse granulation pattern by histology
Participants
6 patients
Outcome
Efficacy of pasireotide
Follow-up
Three to eight months

Main finding

As reported in the abstract

  • Tumour volume reduced in all patients
  • Growth hormone (GH) and IGF-1 levels improved
  • Visual field defects normalised

Observational data: associations, not effects.

Safety

Hyperglycaemia requiring antidiabetic treatment
2 patients

Original publication

Pasireotide as first line medical therapy for selected patients with acromegaly. Pituitary. Published 11 April 2025. doi:10.1007/s11102-025-01514-3

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