دورية أكاديمية

Management of neurofibromatosis type 1-associated plexiform neurofibromas

التفاصيل البيبلوغرافية
العنوان: Management of neurofibromatosis type 1-associated plexiform neurofibromas
المؤلفون: Fisher, Michael J, Blakeley, Jaishri O, Weiss, Brian D, Dombi, Eva, Ahlawat, Shivani, Akshintala, Srivandana, Belzberg, Allan J, Bornhorst, Miriam, Bredella, Miriam A, Cai, Wenli, Ferner, Rosalie E, Gross, Andrea M, Harris, Gordon J, Listernick, Robert, Ly, Ina, Martin, Staci, Mautner, Victor F, Salamon, Johannes M, Salerno, Kilian E, Spinner, Robert J, Staedtke, Verena, Ullrich, Nicole J, Upadhyaya, Meena, Wolters, Pamela L, Yohay, Kaleb, Widemann, Brigitte C
المساهمون: AstraZeneca, Array BioPharma, Exelixis
المصدر: Neuro-Oncology ; volume 24, issue 11, page 1827-1844 ; ISSN 1522-8517 1523-5866
بيانات النشر: Oxford University Press (OUP)
سنة النشر: 2022
الوصف: Plexiform Neurofibromas (PN) are a common manifestation of the genetic disorder neurofibromatosis type 1 (NF1). These benign nerve sheath tumors often cause significant morbidity, with treatment options limited historically to surgery. There have been tremendous advances over the past two decades in our understanding of PN, and the recent regulatory approvals of the MEK inhibitor selumetinib are reshaping the landscape for PN management. At present, there is no agreed upon PN definition, diagnostic evaluation, surveillance strategy, or clear indications for when to initiate treatment and selection of treatment modality. In this review, we address these questions via consensus recommendations from a panel of multidisciplinary NF1 experts.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1093/neuonc/noac146
DOI: 10.1093/neuonc/noac146/45048002/noac146.pdf
الإتاحة: https://doi.org/10.1093/neuonc/noac146Test
https://academic.oup.com/neuro-oncology/article-pdf/24/11/1827/46694452/noac146.pdfTest
رقم الانضمام: edsbas.1B1BC578
قاعدة البيانات: BASE