Long-term pasireotide therapy in acromegaly: extensive real-life experience of a referral center.
- 1. Dipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Diabetologia, Andrologia e Nutrizione, Università Federico II di Napoli, Via S. Pansini 5, 80131, Naples, Italy.
- 2. UNESCO Chair for Health Education and Sustainable Development, Federico II University, Naples, Italy.
- 3. Dipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Diabetologia, Andrologia e Nutrizione, Università Federico II di Napoli, Via S. Pansini 5, 80131, Naples, Italy. colao@unina.it.
- 4. UNESCO Chair for Health Education and Sustainable Development, Federico II University, Naples, Italy. colao@unina.it.
Description
Pasireotide is a novel therapeutic option for patients with acromegaly resistant to first-generation somatostatin receptor ligands. To date, real-life data are still scant, therefore, the aim of the current study is to evaluate the impact of long-term pasireotide therapy on disease control, pituitary tumor size, gluco-insulinemic and lipid profile in a real-life setting.
Retrospective study of data prospectively collected, evaluating hormonal, tumoral, and metabolic data of 28 patients with acromegaly administered with pasireotide in a pituitary tertiary referral center.
Within the first 12 months of treatment, 70.4% of patients achieved normal IGF-I levels, which was maintained at 36-month evaluation in these responders patients. Patients who started with pasireotide 60 mg monthly exhibited significantly lower IGF-I levels after 36 months (p = 0.05) as compared to patients administered first with pasireotide 20 or 40 mg monthly. The maximal tumoral diameter was significantly decreased after 12 months of pasireotide (p < 0.001) and a further reduction was registered throughout the following months, with 41.2% of patients achieving a significant reduction (> 25% of baseline measurement) after 36 months of treatment. Fasting glucose significantly increased during the first 6 months (p < 0.001) with a gradual rise in diabetes prevalence during the following months, resulting diabetes prevalence after 36 months of pasireotide significantly increased compared to baseline (p = 0.003), although with glycated hemoglobin levels within the normal range. Diabetes was managed using oral glucose-lowering drugs or glucagon-like peptide 1 agonists, with no patient requiring insulin therapy. Pasireotide improved lipid profile, mainly during the first 12 months of treatment, by increasing HDL and decreasing triglycerides levels.
Pasireotide is effective and safe in the long-term. Hyperglycemia is a common event and is manageable even without insulin treatment.
© 2024. The Author(s).
Open Access
Licence Attribution (CC BY)
Publisher Website
Access full text
Publication Details
Journal article
Journal:
Journal of endocrinological investigation
Publisher:
Springer Science and Business Media LLC
ISSN:
17208386
Volume:
47
Pages:
1887-1901
Persistent Identifiers
Funding
Financial Support
Università degli Studi di Napoli Federico II
Read more
References
Araujo-Castro M, Pian H, Ruz-Caracuel I, Acitores Cancela A, Pascual-Corrales E,...
Read more
Katznelson L, Laws ER Jr, Melmed S, Molitch ME, Murad MH, Utz A, Wass JA, Endocr...
Read more
Colao A, Pivonello R, Auriemma RS, De Martino MC, Bidlingmaier M, Briganti F, To...
Read more
Henry RR, Ciaraldi TP, Armstrong D, Burke P, Ligueros-Saylan M, Mudaliar S (2013...
Read more
Colao A, Grasso LFS, Giustina A, Melmed S, Chanson P, Pereira AM, Pivonello R. (...
Read more
Showing first 5 of 53 references.
Scholarly Citations
MeSH Terms
MeSH (Medical Subject Headings) is the NLM controlled vocabulary for indexing biomedical articles.
Click any term to view its definition and hierarchy.
Chemical Substances
4 chemical substances identified from Medical Subject Headings (MeSH).