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Endocrine Abstracts (2012) 29 P364

ICEECE2012 Poster Presentations Clinical case reports - Pituitary/Adrenal (58 abstracts)

Antinociceptive effect of pasireotide on octreotide-resistant acromegaly-related headache

D. Marina , M. Klose & U. Feldt-Rasmussen


Rigshospitalet, Copenhagen, Denmark.


Background: Headache often occurs as incapacitating symptom among the patients with acromegaly. GH involvement in the pathophysiologic mechanism and an analgesic effect of somatostatin analogues has been described, but the exact mechanism is not clear. Whether the pan somatostatine (sst)-receptor agonists are superior as concern the antinociceptive effect than the more selective ones is not evidenced.

Case report: A 21-year old woman, diagnosed with acromegaly, presented with visual disturbances and incapacitating headaches lasting for 8 months (MRI: pituitary macroadenoma with supra- and parasellar propagation). Several daily attacks of headache were resistant to high doses of pain-killers. Preoperative neuroendocrine values on oral contraceptives: elevated mean spontaneously GH and insulin-like growth factor (IGF1) (Table 1. apr-09); low-normal free T4 (13.4 pmol/l (14–23 pmol/l)); low levels of FSH <0.2 IU/l and LH <0.1 IU/l; low-normal response to Synacthen test (peak cortisol: 904 nmol/l). After two surgeries in 2009, tumour size was significantly reduced. Different combinations and dose concepts of octreotide, sandostatin LAR and somavert were applied but IGF1 remained high and the headaches worsened. Pasireotide–pegvisomant combination was introduced with prompt marked headache-relief, persisting until few days before next injection. IGF1 normalized for the first time (Table 1. apr-11).

Conclusion: Pasireotide may have a superior antinociceptive effect, as compared to other somatostatin analogues. Very possibly pan-sst receptor agonists may be superior to selective sst2 ones regarding their antinociceptive effect, but further studies are needed to clarify this.

Table 1 Overview of disease activity and medical therapy
DateTherapy for acromegalyGH (mIU/l) IGF1 (ng/ml) IGF1 SD
Apr-09 None >120 (S) 1249 +9
Sep-09 None >120 (S) 1600 +10.68
Jan-10 Octreotide 100 μgx2 Sandostatin LAR 20 mg/month72.9 (OGTT) 1399 +9.69
Apr-10 Octreotide 100 μg at onset of headache Sandostatin LAR 30 mg/month 36.3 (OGTT) 1418 +9.90
Aug-10 Octreotide same Sandostatin LAR 30 mg/2 weeks Somavert 15 mg/day 71.1 (S) 1259 +9.06
Oct-10 Octreotide 100 μg up to 12/day Somavert 15 mgx2 Ipstyl 120 μg/2 weeks 47.7 (OGTT) 583 +4.34
Apr-11 SOM230 40 mg/month (introduced in Jan-11) Somavert same 33.6 (OGTT) 278 +0.89
July-11 SOM230 40 mg/26 days Somavert same 39.06 (S) 246 +0.45
Dec-11 SOM230 same Somavert same 21.2 (OGTT) 342 +1.91
(S): mean spontaneous GH concentration; (OGTT): lowest GH concentration during oral glucose tolerance test.

Declaration of interest: The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research project.

Funding: This research did not receive any specific grant from any funding agency in the public, commercial or not-for-profit sector.

Volume 29

15th International & 14th European Congress of Endocrinology

European Society of Endocrinology 

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