Improving Diagnostic and Therapeutic Outcomes in Pediatric Brain Tumors.
Sydney T GrobJean M Mulcahy LevyPublished in: Molecular diagnosis & therapy (2018)
Pediatric brain tumors are the primary cause of cancer-related death during childhood. Unfortunately, the number of primary and metastatic brain tumors is steadily increasing while the mortality rates for many central nervous system (CNS) lesions have remained stagnant. Molecularly defined tumor classes have been added to the most recent 2016 World Health Organization (WHO) Classification System of Central Nervous System Brain Tumors, driving potential new treatments and identifying targets to improve survival for these patients. Focusing on the genetic mutations most commonly seen in the pediatric CNS tumor population provides the ability to better define tumors based on shared molecular characteristics. Consequently, there is the potential for greater efficacy in targeted therapy to treat these identified genetic aberrations. Understanding the growing importance of molecular diagnosis in pediatric CNS tumors is vital to successfully using novel targeted therapies and improving patient outcomes.
Keyphrases
- blood brain barrier
- end stage renal disease
- squamous cell carcinoma
- small cell lung cancer
- copy number
- ejection fraction
- genome wide
- type diabetes
- cardiovascular disease
- metabolic syndrome
- peritoneal dialysis
- dna methylation
- cardiovascular events
- human health
- adipose tissue
- skeletal muscle
- patient reported outcomes
- insulin resistance
- weight loss
- free survival