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- W2949053103 abstract "Prolactinomas are the most commonly encountered pituitary adenomas in the clinical setting. While most can be controlled by dopamine agonists, a subset of prolactinomas are dopamine-resistant and very aggressive. In such tumors, the treatment of choice is neurosurgery and radiotherapy, with or without temozolomide. Here, we report a patient with an highly aggressive, dopamine-resistant prolactinoma, who only achieved biochemical and tumor control during pasireotide long-acting release (PAS-LAR) therapy, a second-generation somatostatin receptor ligand (SRL). Interestingly, cystic degeneration, tumor cell necrosis or both was observed after PAS-LAR administration suggesting an antitumor effect. This case shows that PAS-LAR therapy holds clinical potential in selective aggressive, dopamine-resistant prolactinomas that express somatostatin (SST) receptor subtype 5 and appears to be a potential new treatment option before starting temozolomide. In addition, PAS-LAR therapy may induce cystic degeneration, tumor cell necrosis or both in prolactinomas." @default.
- W2949053103 created "2019-06-14" @default.
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- W2949053103 date "2019-08-01" @default.
- W2949053103 modified "2023-10-15" @default.
- W2949053103 title "Excellent response to pasireotide therapy in an aggressive and dopamine-resistant prolactinoma" @default.
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- W2949053103 doi "https://doi.org/10.1530/eje-19-0279" @default.
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