Poster Presentation ESA-SRB Conference 2015

Acromegaly: Outcomes from a single pituitary surgeon service in Christchurch New Zealand (#248)

Thomas Upton 1 , Steven Soule 1 , Penny Hunt 1
  1. Canterbury District Health Board, Christchurch, New Zealand

Background: Acromegaly is characterised by excess growth hormone secretion and is associated with increased morbidity and mortality. Current guidelines define cure or control as normal IGF-1 and random growth hormone concentrations <1microg/L (1).

Objective: To audit the immediate and long-term outcomes of patients treated surgically for acromegaly at Christchurch Hospital, New Zealand, a small tertiary referral centre with a single pituitary neurosurgeon.

Methods: We undertook a retrospective case review of all cases of acromegaly treated via endoscopic transnasal transphenoidal surgery between May 2000 and August 2013. Biochemical and clinical data concerning pre-operative findings, post-surgical outcome and long-term follow-up was collected.

Results: 40 patients (15 male, 25 female) were identified. 12 tumours were microadenomas, and 28 macroadenomas. All patients had at least one measurement of random GH and IGF-1 within 6 months of surgery (mean 44 days, range 2-105). 50% (6/12) of microadenomas met cure criteria compared with 35% of macroadenomas (10/28). Three patients with invasive tumours underwent stereotactic radiotherapy and 8 patients commenced medical therapy within 6 months of surgery.

Average follow-up was 70.1 months for 36/40 patients. 41% of patients were on medical therapy (octreotide, cabergoline or in combination), 50% of macroadenomas, 30% of microadenomas. 64% of patients had both IGF-1 and GH within target range; 54% of macroadenomas and 83% of microadenomas. 3 macroadenomas were controlled with cabergoline alone. 33/36 tumours had normal IGF-1. Mean random GH concentrations for macroadenomas was 0.90ug/L, for invasive tumours 1.66ug/L, and 0.58ug/L for microadenomas.

Conclusions: Surgical cure rates for microadenoma are lower than reported elsewhere in the literature but may not reflect true growth hormone status as many patients were assessed less than 3 months following surgery. Consistent measurement of growth parameters at least 3-6 months after surgery is recommended. Most patients achieved good biochemical control at long term follow-up although many require ongoing medical therapy. Cabergoline is an effective therapy even in patients with macroadenoma.

  1. Katznelson, L., Laws, E. R., Melmed, S., Molitch, M. E., Murad, M. H., Utz, A., & Wass, J. a. H. (2014). Acromegaly: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology & Metabolism, (October), jc.2014–2700. doi:10.1210/jc.2014-2700