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[Aggressive pituitary tumors and carcinomas: modern classification, advances and prospects in treatment]. / Agressivnye opukholi i kartsinomy gipofiza: sovremennaya klassifikatsiya, dostizheniya i perspektivy v lechenii.
Astafyeva, L I; Kalinin, P L; Kobyakov, G L; Trunin, Yu Yu; Ryzhova, M V.
Affiliation
  • Astafyeva LI; Burdenko Neurosurgical Center, Moscow, Russia.
  • Kalinin PL; Burdenko Neurosurgical Center, Moscow, Russia.
  • Kobyakov GL; Burdenko Neurosurgical Center, Moscow, Russia.
  • Trunin YY; Burdenko Neurosurgical Center, Moscow, Russia.
  • Ryzhova MV; Burdenko Neurosurgical Center, Moscow, Russia.
Zh Vopr Neirokhir Im N N Burdenko ; 88(3): 103-110, 2024.
Article in Ru | MEDLINE | ID: mdl-38881023
ABSTRACT
Despite slow growth of most pituitary tumors and high rates of total resection and/or effective therapy, pituitary neoplasms are characterized by aggressive behavior with high growth rate, frequent relapses and resistance to standard treatments in 10% of cases. In modern WHO classifications of tumors of the central nervous system, endocrine and neuroendocrine tumors, the authors propose the definition «pituitary neuroendocrine tumor¼ instead of previous «pituitary adenoma¼ and «metastasizing pituitary neuroendocrine tumor¼ instead of «pituitary carcinoma¼. Currently, there are no effective prognostic markers of aggressive tumors. This complicates early diagnosis. It is proposed to apply a five-stage prognostic classification based on proliferation rate (including mitotic count, Ki-67 index and p53 immunoexpression) and morphometric markers of invasiveness for all resected pituitary neoplasms. This approach would be valuable for earlier detection of aggressive tumors and pituitary carcinomas. Compression of visual pathways, third ventricle and brain stem due to rapid growth of aggressive tumors usually requires redo surgeries with subsequent radiotherapy. Hormonally active tumors require therapy with somatostatin analogues and dopamine agonists in maximum possible doses. Chemotherapy with temozolomide as first-line option is recommended if standard treatment is ineffective. Alternative treatment includes peptide receptor radionuclide therapy (PRRT), molecular targeted therapy (bevacizumab, tyrosine kinase inhibitors, everolimus and cyclin-dependent kinase inhibitors) and immunotherapy (checkpoint inhibitors). Considering the need for combined treatment, these cases should always be discussed by a multidisciplinary team (neurosurgeon, endocrinologist, radiotherapist, oncologist, pathologist) with necessary qualifications and experience in treating these patients. Treatment of aggressive tumors and pituitary carcinomas is becoming an active and rapidly developing direction in neurosurgery, endocrinology and oncology.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pituitary Neoplasms Limits: Humans Language: Ru Journal: Zh Vopr Neirokhir Im N N Burdenko Year: 2024 Document type: Article Affiliation country: Rusia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pituitary Neoplasms Limits: Humans Language: Ru Journal: Zh Vopr Neirokhir Im N N Burdenko Year: 2024 Document type: Article Affiliation country: Rusia