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PMID: 33721151 Published · epublish English

Neurofibromatosis in the Era of Precision Medicine: Development of MEK Inhibitors and Recent Successes with Selumetinib.

Current oncology reports ·Vol. 23 ·No. 4 ·2021-00-15

Galvin R, Watson AL, Largaespada DA, Ratner N, Osum S, Moertel CL

Abstract

Patients with neurofibromatosis type 1 (NF1) are at increased risk for benign and malignant neoplasms. Recently, targeted therapy with the MEK inhibitor class has helped address these needs. We highlight recent successes with selumetinib while acknowledging ongoing challenges for NF1 patients and future directions. MEK inhibitors have demonstrated efficacy for NF1-related conditions, including plexiform neurofibromas and low-grade gliomas, two common causes of NF1-related morbidity. Active investigations for NF1-related neoplasms have benefited from advanced understanding of the genomic and cell signaling alterations in these conditions and development of sound preclinical animal models. Selumetinib has become the first FDA-approved targeted therapy for NF1 following its demonstrated efficacy for inoperable plexiform neurofibroma. Investigations of combination therapy and the development of a representative NF1 swine model hold promise for translating therapies for other NF1-associated pathology.

Keywords
Combination therapy Low-grade glioma MEK inhibitor Malignant peripheral nerve sheath tumor Neurofibromatosis Optic pathway glioma Plexiform neurofibroma Selumetinib
Article Info
Journal
Current oncology reports
Abbr.
Curr Oncol Rep
ISSN
1534-6269
Corresponding email
Published
2021-00-15
Language
English
Country/Region
United States
NLM ID
100888967
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