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Recent Update in Pharmacological Agents for Optic Pathway Glioma

Optic pathway gliomas (OPGs) are insidious, debilitating low-grade tumors. They can affect the optic nerve, optic chiasm, and optic tracts and can be sporadic or associated with neurofibromatosis type 1 (NF1). The location of OPGs within the optic pathway typically precludes complete resection or op...

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Autor principal: Park, Meerim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098979/
https://www.ncbi.nlm.nih.gov/pubmed/35545829
http://dx.doi.org/10.14791/btrt.2022.0006
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author Park, Meerim
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description Optic pathway gliomas (OPGs) are insidious, debilitating low-grade tumors. They can affect the optic nerve, optic chiasm, and optic tracts and can be sporadic or associated with neurofibromatosis type 1 (NF1). The location of OPGs within the optic pathway typically precludes complete resection or optimal radiation dose. Treatment is unnecessary for sporadic and NF1-related OPGs that do not cause visual impairments. Chemotherapy is the mainstay of treatment for patients with progressive disease. However, outcomes following standard treatments have been mixed, and standardized outcome measurements are lacking. In recent years, newer molecularly targeted therapies such as anti-vascular endothelial growth factor (VEGF) monoclonal antibody, mitogen-activated protein kinase (MAPK) inhibitor, and mammalian target of rapamycin (mTOR) inhibitor, represent a promising treatment modality.
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spelling pubmed-90989792022-05-19 Recent Update in Pharmacological Agents for Optic Pathway Glioma Park, Meerim Brain Tumor Res Treat Review Article Optic pathway gliomas (OPGs) are insidious, debilitating low-grade tumors. They can affect the optic nerve, optic chiasm, and optic tracts and can be sporadic or associated with neurofibromatosis type 1 (NF1). The location of OPGs within the optic pathway typically precludes complete resection or optimal radiation dose. Treatment is unnecessary for sporadic and NF1-related OPGs that do not cause visual impairments. Chemotherapy is the mainstay of treatment for patients with progressive disease. However, outcomes following standard treatments have been mixed, and standardized outcome measurements are lacking. In recent years, newer molecularly targeted therapies such as anti-vascular endothelial growth factor (VEGF) monoclonal antibody, mitogen-activated protein kinase (MAPK) inhibitor, and mammalian target of rapamycin (mTOR) inhibitor, represent a promising treatment modality. The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology 2022-04 2022-04-29 /pmc/articles/PMC9098979/ /pubmed/35545829 http://dx.doi.org/10.14791/btrt.2022.0006 Text en Copyright © 2022 The Korean Brain Tumor Society, The Korean Society for Neuro-Oncology, and The Korean Society for Pediatric Neuro-Oncology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Park, Meerim
Recent Update in Pharmacological Agents for Optic Pathway Glioma
title Recent Update in Pharmacological Agents for Optic Pathway Glioma
title_full Recent Update in Pharmacological Agents for Optic Pathway Glioma
title_fullStr Recent Update in Pharmacological Agents for Optic Pathway Glioma
title_full_unstemmed Recent Update in Pharmacological Agents for Optic Pathway Glioma
title_short Recent Update in Pharmacological Agents for Optic Pathway Glioma
title_sort recent update in pharmacological agents for optic pathway glioma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098979/
https://www.ncbi.nlm.nih.gov/pubmed/35545829
http://dx.doi.org/10.14791/btrt.2022.0006
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