Therapeutic efforts for NF-1-associated tumors have centered around inhibiting Ras output, leading to the clinical success of downstream MEK inhibition for plexiform neurofibromas and low-grade gliomas. However, MEK inhibition and similar molecular monotherapy approaches that block Ras signaling do not work for all patients and show limited efficacy for more aggressive cancers such as malignant peripheral nerve sheath tumors and high-grade gliomas, motivating novel treatment approaches. We highlight the current therapeutic landscape for NF-1-associated tumors, broadly categorizing treatment into past strategies for serial Ras pathway blockade, current approaches targeting parallel oncogenic and tumor suppressor pathways, and future avenues of investigation leveraging biologic and technical innovations in immunotherapy, pharmacology, and gene delivery.
Keyphrases
- high grade
- low grade
- signaling pathway
- pi k akt
- peripheral nerve
- lps induced
- oxidative stress
- nuclear factor
- end stage renal disease
- combination therapy
- rheumatoid arthritis
- wild type
- randomized controlled trial
- clinical trial
- chronic kidney disease
- single molecule
- current status
- quality improvement
- young adults
- cancer therapy