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Aggressive prolactinomas: how to manage?
Hélène Lasolle1,2,3, Mirela Diana Ilie4, Gérald Raverot5,6,7
1INSERM U1052, CNRS UMR5286, Cancer Research Center of Lyon, 69008, Lyon, Auvergne-Rhône-Alpes, France.
Aggressive prolactinomas are rare, invasive tumors. Temozolomide offers a treatment option, controlling growth in 50% of cases, but new therapies are needed for resistant or recurring pituitary tumors.
Area of Science:
- Endocrinology
- Neuro-oncology
- Oncology
Background:
- Aggressive prolactinomas are invasive pituitary tumors resistant to standard treatments.
- Prolactin carcinomas, a form of pituitary carcinoma, can metastasize.
Purpose of the Study:
- To review current treatment strategies for aggressive pituitary prolactinomas and carcinomas.
- To identify effective therapies beyond standard dopamine agonist treatment, surgery, and radiotherapy.
Main Methods:
- Literature search on the treatment of aggressive prolactinomas and carcinomas.
- Review of data on efficacy and outcomes of various therapeutic interventions.
Main Results:
- Temozolomide is the current best option for aggressive prolactinomas, controlling tumor growth in approximately 50% of patients.
- Long-term complete response to temozolomide is limited; alternative drugs like pasireotide or peptide receptor radionuclide therapy may be considered.
- Temozolomide improves overall survival but does not guarantee a cure for all patients.
Conclusions:
- Despite temozolomide's benefits, a significant proportion of aggressive prolactinomas remain resistant or recur.
- There is a persistent need for novel therapeutic agents to manage these rare and aggressive pituitary tumors.
- Access to clinical trials for rare cancers, including tyrosine kinase inhibitors and immunotherapy, is crucial for patients with aggressive prolactinomas.
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