Combined treatment for acromegaly with long-acting somatostatin analogs and pegvisomant: long-term safety for up to 4.5 years (median 2.2 years) of follow-up in 86 patients.
BACKGROUND: We previously reported on the efficacy, safety, and quality of life (QoL) of long-acting somatostatin analogs (SSA) and (twice) weekly pegvisomant (PEG-V) in acromegaly and improvement after the addition of PEG-V to long-acting SSA. OBJECTIVE: To assess the long-term safety in a larger group of acromegalic patients over a larger period of time: 29.2 (1.2-57.4) months (mean (range)). DESIGN: Pegvisomant was added to SSA monotherapy in 86 subjects (37 females), to normalize serum IGF1 concentrations (n=63) or to increase the QoL. The median dosage was 60.0 (20-200) mg weekly. RESULTS: After a mean treatment period of 29.2 months, 23 patients showed dose-independent PEG-V related transient liver enzyme elevations (TLEE). TLEE occurred only once during the continuation of combination therapy, but discontinuation and re-challenge induced a second episode of TLEE. Ten of these patients with TLEE also suffered from diabetes mellitus (DM). In our present series, DM had a 2.28 odds ratio (CI 1.16-9.22; p=0.03) higher risk for developing TLEE. During the combined therapy, a clinical significant decrease in tumor size by more than 20% was observed in 14 patients. Two of these patients were previously treated by pituitary surgery, 1 with additional radiotherapy and all other patients received primary medical treatment. CONCLUSION: Long-term combined treatment with SSA and twice weekly PEG-V up to more than 4 years seems to be safe. Patients with both acromegaly and DM have a 2.28 higher risk of developing TLEE. Clinical significant tumor shrinkage was observed in 14 patients during combined treatment.
|Keywords||acromegaly, adult, aged, angiopeptin, article, cyclopeptide, diabetes mellitus, drug antagonism, drug combination, drug derivative, electrocardiography, female, follow up, growth hormone receptor, human, human growth hormone, liver function test, male, middle aged, octreotide, pathophysiology, pegvisomant, somatostatin|
|Persistent URL||dx.doi.org/10.1530/EJE-08-0843, hdl.handle.net/1765/16093|
|Journal||European Journal of Endocrinology|
Neggers, S.J.C.M.M, de Herder, W.W, Janssen, J.A.M.J.L, Feelders, R.A, & van der Lely, A-J. (2009). Combined treatment for acromegaly with long-acting somatostatin analogs and pegvisomant: long-term safety for up to 4.5 years (median 2.2 years) of follow-up in 86 patients.. European Journal of Endocrinology (Vol. 160, pp. 529–533). doi:10.1530/EJE-08-0843