Abstract
Context
Treatment with somatostatin receptor ligands (SRLs) is often given before pituitary surgery to patients with acromegaly.
Objective
To study whether the response to treatment with SRLs is predictive of surgical outcome.
Design
Retrospective, observational study.
Setting
Tertiary care center.
Patients
We investigated 272 patients with acromegaly who had been treated with an SRL between 1990 and 2018.
Intervention
All patients underwent pituitary surgery performed by a skilled neurosurgeon.
Main outcome measure
Outcome of pituitary surgery in patients who had normalization of insulin-like growth factor 1 (IGF-1) levels during SRL therapy in comparison with patients who did not normalize IGF-1 levels.
Results
Normalization of IGF-1 levels during SRL treatment occurred in 62 patients (22.8%) and was similar for the 3 different types of SRL (P = .88). Surgical remission occurred in 59.6% of the patients. Patients who normalized IGF-1 levels during SRL treatment had a higher probability of surgical cure than patients without IGF-1 normalization (83.9% vs 52.4%, respectively; P < .001). Multivariate analysis confirmed that lack of cavernous sinus invasion, small maximum tumor diameter, and IGF-1 normalization during SRL therapy were the only factors independently associated with a favorable surgical outcome.
Conclusions
Our study demonstrates that the normalization of IGF-1 levels during treatment with SRLs is an independent predictive factor of a favorable surgical outcome. The underlying mechanisms remain unclear, but an optimal response to medical therapy may be a characteristic of less aggressive tumors that are more likely to be entirely removed at surgery.
Overview publication
| Title | Normal Insulin-like Growth Factor 1 During Somatostatin Receptor Ligand Treatment Predicts Surgical Cure in Acromegaly |
| Date | September 1st, 2020 |
| Issue name | The Journal of Clinical Endocrinology & Metabolism |
| Issue number | v105.9 pe3339-e3347 |
| DOI | 10.1210/clinem/dgaa424 |
| Authors | |
| MTGs | MTG6 |
| Read | Read publication |
