4.3 Article

De-escalation treatment with pasireotide for acromegaly: a long-term experience

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ENDOCRINE
卷 80, 期 3, 页码 505-510

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SPRINGER
DOI: 10.1007/s12020-023-03325-7

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Acromegaly; Pasireotide LAR; High dose; Somatostatin receptors; Somatostatin analogues; Aggressive acromegaly

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This study reports three cases of resistant acromegaly treated with a de-escalation approach using pasireotide LAR. The results showed that de-escalation treatment with pasireotide LAR may allow a greater proportion of patients to achieve control of acromegaly, especially in clinically aggressive cases. Although there may be a risk of hyperglycemia, it can be controlled with oral antidiabetic medications.
IntroductionPasireotide long-acting release (LAR) is approved for second-line treatment of acromegaly. Starting pasireotide LAR 40 mg every 4 weeks is recommended and then up-titrate to 60 mg monthly in case of IGF-I uncontrolled levels. We present three patients treated with a de-escalation approach with pasireotide LAR.Case 1A 61-year-old female diagnosed with resistant acromegaly was treated with pasireotide LAR 60 mg every 28 days. When IGF-I reached the lower age range, therapy was decreased to pasireotide LAR 40 mg and then to 20 mg. In 2021 and 2022, IGF-I value remained within the normal range.Case 2A 40-year-old female diagnosed with resistant acromegaly underwent three neurosurgeries. In 2011, she was enrolled in the PAOLA study and assigned to pasireotide LAR 60 mg. Due to IGF-I overcontrol and radiological stability, therapy was downscaled to 40 mg in 2016 and to 20 mg in 2019. The patient developed hyperglycemia, which was treated with metformin.Case 3A 37-year-old male diagnosed with resistant acromegaly was treated with pasireotide LAR 60 mg in 2011. In 2018, therapy was decreased to 40 mg due to IGF-I overcontrol and in 2022 to 20 mg. He developed hyperglycemia, but HbA1c values remained under 48 nmol/L for 7 years.ConclusionDe-escalation treatment with pasireotide LAR may allow a greater proportion of patients to achieve control of acromegaly, particularly in selected cases of clinically aggressive acromegaly potentially responsive to pasireotide (high IGF-I values, invasion of the cavernous sinuses, partial resistance to first-line somatostatin analogues and positive expression of somatostatin receptor 5). Another benefit may be IGF-I oversuppression overtime. The major risk seems to be hyperglycemia.

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