TY - JOUR
T1 - Pediatric Central Nervous System Cancers, Version 2.2023
AU - Gajjar, Amar
AU - Mahajan, Anita
AU - Abdelbaki, Mohamed
AU - Anderson, Clarke
AU - Antony, Reuben
AU - Bale, Tejus
AU - Bindra, Ranjit
AU - Bowers, Daniel C.
AU - Cohen, Kenneth
AU - Cole, Bonnie
AU - Dorris, Kathleen
AU - Ermoian, Ralph
AU - Franson, Andrea
AU - Helgager, Jeffrey
AU - Landi, Daniel
AU - Lin, Chi
AU - Metrock, Laura
AU - Nanda, Ronica
AU - Palmer, Joshua
AU - Partap, Sonia
AU - Plant, Ashley
AU - Pruthi, Sumit
AU - Reynolds, Renee
AU - Ruggieri, Paul
AU - Stearns, Duncan
AU - Storm, Phillip
AU - Wang, Anthony
AU - Warren, Katherine
AU - Whipple, Nicholas
AU - Zaky, Wafik
AU - McMillian, Nicole R.
AU - Pluchino, Lenora A.
N1 - Publisher Copyright:
© 2022 Harborside Press. All rights reserved.
PY - 2022/12
Y1 - 2022/12
N2 - Central nervous system (CNS) cancers account for approximately one quarter of all pediatric tumors and are the leading cause of cancerrelated death in children.More than 4,000 brain and CNS tumors are diagnosed each year in children and teens, and the incidence rate has remained stagnant in recent years. Themost commonmalignant pediatric CNS tumors are gliomas, embryonal tumors consisting of predominately medulloblastomas, and germ cell tumors. The inaugural version of the NCCNGuidelines for Pediatric CentralNervous SystemCancers focuses on the diagnosis and management of patients with pediatric diffuse high-grade gliomas. The information contained in the NCCN Guidelines is designed to help clinicians navigate the complex management of pediatric patients with diffuse high-grade gliomas. The prognosis for these highly aggressive tumors is generally poor, with 5-year survival rates of ,20% despite the use of combinedmodality therapies of surgery, radiation therapy and systemic therapy. Recent advances in molecular profiling has expanded the use of targeted therapies in patients whose tumors harbor certain alterations. However, enrollment in a clinical trial is the preferred treatment for eligible patients.
AB - Central nervous system (CNS) cancers account for approximately one quarter of all pediatric tumors and are the leading cause of cancerrelated death in children.More than 4,000 brain and CNS tumors are diagnosed each year in children and teens, and the incidence rate has remained stagnant in recent years. Themost commonmalignant pediatric CNS tumors are gliomas, embryonal tumors consisting of predominately medulloblastomas, and germ cell tumors. The inaugural version of the NCCNGuidelines for Pediatric CentralNervous SystemCancers focuses on the diagnosis and management of patients with pediatric diffuse high-grade gliomas. The information contained in the NCCN Guidelines is designed to help clinicians navigate the complex management of pediatric patients with diffuse high-grade gliomas. The prognosis for these highly aggressive tumors is generally poor, with 5-year survival rates of ,20% despite the use of combinedmodality therapies of surgery, radiation therapy and systemic therapy. Recent advances in molecular profiling has expanded the use of targeted therapies in patients whose tumors harbor certain alterations. However, enrollment in a clinical trial is the preferred treatment for eligible patients.
UR - http://www.scopus.com/inward/record.url?scp=85143994074&partnerID=8YFLogxK
U2 - 10.6004/jnccn.2022.0062
DO - 10.6004/jnccn.2022.0062
M3 - Article
C2 - 36509072
AN - SCOPUS:85143994074
SN - 1540-1405
VL - 20
SP - 1339
EP - 1362
JO - JNCCN Journal of the National Comprehensive Cancer Network
JF - JNCCN Journal of the National Comprehensive Cancer Network
IS - 12
ER -