Evidence map›Paper›PMID 39082175›Full record

ArticleEndocrine, metabolic & immune disorders drug targets2025

Long-term Remission in Functioning Pituitary Adenomas after Medical Therapy Withdrawal: A Chance for Cushing's Disease.

Alessandro Mondin, Filippo Ceccato, Carla Scaroni, Mattia Barbot

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Article in Endocrine, metabolic & immune disorders drug targets, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Alessandro MondinDepartment of Medicine-DIMED, University of Padova, Padova, Italy.ORCID 0000-0002-6046-5198
Filippo CeccatoDepartment of Medicine-DIMED, University of Padova, Padova, Italy.ORCID 0000-0003-1456-8716
Carla ScaroniDepartment of Medicine-DIMED, University of Padova, Padova, Italy.ORCID 0000-0001-9396-3815
Mattia BarbotDepartment of Medicine-DIMED, University of Padova, Padova, Italy.ORCID 0000-0002-1081-5727

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe possibility of sustained disease remission in functioning pituitary adenomas after drug withdrawal is well-known for prolactinomas and it has also been described in a subset of acromegalic patients. On the contrary, medical treatment for Cushing's Disease (CD) is generally considered a life-long measure except for previously radio-treated patients. Sparse evidence of spontaneous remissions in CD has been reported, mainly related to a possible pituitary tumor apoplexy. To the best of our knowledge, none of these cases has included the use of a pituitary targeting agent. CASE PRESENTATION: Herein, we have reported the case of a radiotherapy-naïve patient with persistent CD after pituitary surgery who participated in the CSOMG230 trials, presenting sustained remission after Long-acting Release (LAR) pasireotide withdrawal. Under monthly pasireotide LAR 40 mg, the patient achieved urinary hormone control and clinical signs of cortisol excess normalization. After 8 years of treatment, the patient completed the study protocol and had to withdraw the drug as it was no longer available for CD in Italy. Before starting new therapies, we reassessed hormone levels that were surprisingly within normal ranges. At 24 months after the last dose of pasireotide, the patient was still in clinical and biochemical full remission. We have also briefly reviewed previous cases of sustained remission after somatostatin analogues withdrawal in other functioning pituitary adenomas.

conclusionFar from the general rule, this case suggests that prolonged treatment with pasireotide LAR might induce a durable CD remission. A dose down-titration/suspension might be considered in patients well-controlled on long-term therapy and with negative pituitary imaging. However, close monitoring is recommended given the high rate of complications in untreated patients.

Indexed as

AdenomaPituitary ACTH HypersecretionPituitary NeoplasmsSomatostatinWithholding TreatmentHumansRemission InductionTime FactorsTreatment OutcomepasireotideSomatostatinCD remissionCushing’s diseasemedical therapypasireotide LARpituitary adenomas.somatostatin analogues

Identifiers

PMID39082175
PMCPMC12376123

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