Pharmacological treatment strategies for subependymal giant cell astrocytoma (SEGA)

التفاصيل البيبلوغرافية
العنوان: Pharmacological treatment strategies for subependymal giant cell astrocytoma (SEGA)
المؤلفون: David Neal Franz, Daniel Ebrahimi-Fakhari
المصدر: Expert Opinion on Pharmacotherapy. 21:1329-1336
بيانات النشر: Informa UK Limited, 2020.
سنة النشر: 2020
مصطلحات موضوعية: medicine.medical_specialty, Antineoplastic Agents, Astrocytoma, Tuberous Sclerosis Complex 1 Protein, 03 medical and health sciences, Tuberous sclerosis, 0302 clinical medicine, Tuberous Sclerosis, Tuberous Sclerosis Complex 2 Protein, Cerebrospinal fluid diversion, Subependymal zone, Humans, Medicine, Pharmacology (medical), Child, Pharmacology, Everolimus, Subependymal giant cell astrocytoma, Brain Neoplasms, business.industry, TOR Serine-Threonine Kinases, General Medicine, medicine.disease, Hydrocephalus, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Sirolimus, Mutation, Radiology, TSC1, business, 030217 neurology & neurosurgery, medicine.drug
الوصف: Introduction Subependymal ependymal giant cell astrocytomas (SEGAs) occur almost exclusively in the setting of tuberous sclerosis (TSC). They are low-grade gliomas which typically produce clinical symptoms through either mass effect or hydrocephalus. As do other manifestations of tuberous sclerosis, these lesions result from mutations in either the TSC1 or the TSC2 gene. These mutations cause hyperactivation of the mechanistic target of rapamycin (mTOR). In view of their tendency to grow slowly, clinical symptoms usually only occur when the tumors reach a considerable size. Therapy can involve surgical resection, cerebrospinal fluid diversion, or medical therapy with an mTOR inhibitor. Areas covered Herein, the authors discuss the diagnosis, symptoms, and practical management of SEGAs as well as providing their expert opinion. Expert opinion mTOR inhibitors have largely replaced surgery as the primary modality for the management of SEGAs. Surgical treatment is largely limited to tumors that present with acute hydrocephalus and increased intracranial pressure. Patients with TSC should undergo periodic screening with CT or preferably MRI scans of the brain from childhood to approximately age 25 to identify SEGAs which require treatment. In addition to avoiding potential morbidity associated with surgical resection, mTOR inhibitors have the potential to improve the clinical status of tuberous sclerosis patients generally.
تدمد: 1744-7666
1465-6566
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc74d9cbb8bbf37fdb23039a7cacf2c9Test
https://doi.org/10.1080/14656566.2020.1751124Test
رقم الانضمام: edsair.doi.dedup.....dc74d9cbb8bbf37fdb23039a7cacf2c9
قاعدة البيانات: OpenAIRE