Everolimus for Subependymal Giant-Cell Astrocytomas in Tuberous Sclerosis
By J. Stockman. 2012
595 citations recorded by the source corpus.
Subfields: Neurology, Physiology, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/5628b5bb2afcc4834d526e411e65a23147e18cb2
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Citations in the corpus
- Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference (2013, background): “Twelve subcommittees, each led by a clinician with advanced expertise in TSC and the relevant medical subspecialty, were organized to focus on specific disease focus topics that have important clinical management implications in TSC: (1) dermatology and dentistry; (2) nephrology; (3) pulmonology; (4”
- Multi-compartment microscopic diffusion imaging (2016, background): “Our findings have clear translational significance as SMT may help oversee treatment success in promising clinical trials (Franz et al., 2006; Bissler et al., 2008; Krueger et al., 2010; Tillema et al., 2012) where patients receive mTOR inhibitors such as everolimus and sirolimus.”
- Multifaceted role of mTOR (mammalian target of rapamycin) signaling pathway in human health and disease (2023, background): “gov, NCT00411619) in these patients.(268) Everolimus has reported promising anticancer efficacy in patients with pancreatic neuroendocrine tumors during clinical trials (RADIANT-3, NCT00510068) and received FDA approval.”
- Recent progress in pancreatic cancer (2013, background): “For example, the tyrosine kinase inhibitor sunitinib and the mammalian target of rapamycin (mTOR) pathway inhibitor everolimus have both been reported to significantly improve progression-free survival in patients with advanced PanNETs.72,73 Acinar carcinoma and pancreatoblastoma are rare usually so”
- Epidemiologic and Molecular Prognostic Review of Glioblastoma (2014, background): “The success of m-TOR pathway inhibition for subependymal giant-cell astrocytomas and the possibility of identifying a subtype of GBM sensitive to up-front treatment with bevacizumab are examples, but we need much more (142, 143).”