期刊
CHILDS NERVOUS SYSTEM
卷 36, 期 10, 页码 2443-2452出版社
SPRINGER
DOI: 10.1007/s00381-020-04731-2
关键词
Trial design; Neurofibromatosis 1; Plexiform neurofibroma; MEK inhibitor; Clinical trial
资金
- Center for Cancer Research, NCI, NIH Intramural Research Program
- NATIONAL CANCER INSTITUTE [ZIABC010801] Funding Source: NIH RePORTER
Background Neurofibromatosis type 1 (NF1)-related plexiform neurofibromas (pNF) can be debilitating and until recently, surgery was the only potentially effective therapy for these tumors. Methods We review critical steps in the path towards the FDA approval of the first medical therapy for NF1 pNF and the current status of MEK inhbitor therapy. Results Sustained efforts by the NF community have resulted in a detailed understanding of the natural history and biology of NF1-related peripheral nerve sheath tumors. This work provided the basis for the development of meaningful clinical trials targeting pNF. Inhibition of the RAS/MAPK signaling pathway with MEK inhibitors identified the first medical therapy which resulted in shrinkage in the majority of children with NF1 and large inoperable pNF. Based on this finding and subsequent demonstration of clinical benefit, the MEK inhibitor selumetinib recently received approval by the United States Food and Drug Administration (FDA) for children with symptomatic pNF. Conclusions Sustained efforts and collaborations have resulted in identification of MEK inhibitors as effective therapy for NF1 pNF. Future work work will be directed at prevention of pNF morbidity and deepening the reponse in symptomatic pNF.
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