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Updated: Aug 15, 2026

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
Treatment strategies for acromegaly
Ferdinand Roelfsema1, Nienke R Biermasz, Johannes A Romijn
1Department of Endocrinology and Metabolic Diseases, Leiden University Medical Center, The Netherlands. f.roelfsema@lumc.nl
Acromegaly, caused by excess growth hormone (GH), increases mortality risk. Treatments include surgery, radiotherapy, and medications like somatostatin analogs and GH-receptor blockers, aiming to normalize GH and IGF-1 levels.
Area of Science:
- Endocrinology
- Oncology
- Cardiovascular Medicine
Background:
- Acromegaly is a chronic disorder from pituitary adenomas causing excess growth hormone (GH).
- Active acromegaly significantly elevates mortality risk, primarily due to cardiovascular disease.
- Surgical cure rates for acromegaly are around 60%, necessitating alternative and adjuvant therapies.
Purpose of the Study:
- To review the pathophysiology of acromegaly.
- To evaluate current medical treatments, including somatostatin analogs and pegvisomant.
- To discuss emerging therapeutic agents for acromegaly management.
Main Methods:
- Literature review of acromegaly pathophysiology and treatment modalities.
- Analysis of safety and efficacy data for somatostatin analogs and GH-receptor antagonists.
- Examination of clinical trial data for novel acromegaly therapeutics.
Main Results:
- Transsphenoidal surgery offers rapid cure but does not achieve universal success.
- Somatostatin analogs are effective in 50-60% of patients but lack mortality data.
- Pegvisomant normalizes IGF-1 in nearly all patients, representing a significant advancement.
Conclusions:
- Acromegaly management requires a multi-modal approach due to incomplete surgical efficacy.
- Medical therapies, including somatostatin analogs and pegvisomant, play crucial roles in controlling GH excess.
- Ongoing research into new drugs promises improved outcomes for acromegaly patients.
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