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Endocrine Abstracts (2024) 99 EP468 | DOI: 10.1530/endoabs.99.EP468

ECE2024 Eposter Presentations Pituitary and Neuroendocrinology (214 abstracts)

Pasireotide as first line medical therapy for treatment of selected patients with acromegaly

Nicoleta Olarescu 1,2,3 , Jens Bollerslev 1,2 , Anders Jørgensen 1,2 & Ansgar Heck 1


1Section of Specialized Endocrinology, Department of Endocrinology, Oslo University Hospital (OUS), Oslo;2Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway;3Research Institute of Internal Medicine, Oslo University Hospital (OUS), Oslo, Norway


Objective: Pasireotide is a second-generation somatostatin receptor ligands (SRLs) with highest affinity for somatostatin receptor (SST)5, followed by SST2. It is considered, so far, in patients resistant to first-generation SRLs, after surgical failure. Histological characteristics and T2-weighted MRI can predict resistance to first-generation SRLs in patients with somatotroph adenomas. Previous studies primarily assessed efficacy of pasireotide as 2nd or 3rd line medical treatment. However, pasireotide might be an option in patients expected to be resistant to first-generation SRLs (e.g. hyperintensity T2-weighted MRI signal and/or sparsely granulated immunohistochemical pattern). We describe the efficacy of pasireotide as the first pharmacological treatment.

Methods: Clinical and biochemical parameters, T2-weighted MRI signal intensity, histological diagnosis and efficacy of pasireotide treatment on GH and IGF-1 levels, and tumour volume (by ellipsoid formula), were recorded in four patients (two treated as primary treatment, two after debulking surgery), expected to be resistant to first-generation SRL.

Results: Table 1 presents age, GH and IGF-1 levels, and tumour volume before and after treatment with pasireotide median 5.6 (range 4.5-6.6) months. All tumours were hyperintense on T2-weighted MRI and sparsely granulated somatotroph adenomas were identified in the operated patients. Variability in GH and IGF-1 reduction was observed. Tumour volume decreased at least with 31% and the effect occured early. One patient started ad-on cabergoline therapy two months after pasireotide. At last visit, 18-58 months after treatment initiation, all patients still received pasireotide, two in combination with pegvisomant, one with cabergoline and one patient was additionally treated by radiotherapy. Two patients had normalised IGF-1, two patients further improved IGF-1. HbA1c remained stable in two patients and worsened in two patients with further need of anti-diabetic treatment.

Table 1. Patients’ characteristics before and after treatment with pasireotide
BaselineFollow-upChange (%)
sexAge yrsGH µg/lIGF-1 nmol/lIGF-1/ULNTumour volume cm3GH µg/lIGF-1 nmol/lIGF-1/ULNTumour volume cm3GHIGF-1Tumour volume
#1_female314.0682.374472.1260.94556476239
#2_male512.9602.7471582.7582.6285407339
#3_female351.6551.954571.5391.3374962931
#4_female30200.01143.977583.8813.83360982956

Conclusions: In patients with T2-hyperintense MRI adenomas and presumed resistance to first-generation SRLs, pasireotide may be considered as first line medical treatment, facilitating rapid tumour control and decreased disease activity.

Volume 99

26th European Congress of Endocrinology

Stockholm, Sweden
11 May 2024 - 14 May 2024

European Society of Endocrinology 

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