Pediatric Neurofibromatosis: What’s Next for the Rare Tumor Syndrome? – Oncology Nursing News

Until recently, there was no FDA-approved therapy for pediatric patients with neurofibromatosis type 1 (NF1), a genetic disorder that causes tumor growth – which could become cancerous – in young children.

On April 10, the FDA approved selumetinib (Koselugo) for children over the age of 2 who have inoperable or symptomatic plexiform (PNs) – tumors on nerve sheaths. NF1-related tumors can drastically impair a patient’s daily function, be incredibly painful, and turn into cancerous tumors as well.

Click here to read full article https://www.oncnursingnews.com/web-exclusives/pediatric-neurofibromatosis-whats-next-for-the-rare-tumor-syndrome

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