| Literature DB >> 34671804 |
Hideo Nakamura1, Hirokazu Takami2, Takaaki Yanagisawa3, Toshihiro Kumabe4, Takamitsu Fujimaki5, Yoshiki Arakawa6, Katsuyuki Karasawa7, Keita Terashima8, Hideaki Yokoo9, Kohei Fukuoka10, Yukihiko Sonoda11, Kaori Sakurada11, Yohei Mineharu6, Toshinori Soejima12, Motoaki Fujii13, Naoki Shinojima14, Junichi Hara15, Kai Yamasaki15, Junya Fujimura16, Fumiyuki Yamasaki17, Mayu Takahashi18, Tomonari Suzuki19, Iori Sato20, Ryo Nishikawa19, Kazuhiko Sugiyama21.
Abstract
Primary CNS germ cell tumors (GCTs) are rare neoplasms predominantly observed in the pediatric and young adult populations. In line with the hypothesis that the primordial germ cell is the cell-of-origin, histopathological examinations for this pathology involve a diverse range of components mirroring the embryogenic developmental dimensions. Chemotherapy and radiotherapy are the mainstays of treatment, with surgery having a limited role for diagnosis and debulking of residual tissue after treatment. While better management has been achieved over recent decades by modifying radiation coverage and selecting appropriate chemotherapy, standardization of treatment remains challenging, partly due to the low volume of cases encountered in each institution. As the incidence is higher in East Asia, including Japan, the Japan Society for Neuro-Oncology established a multidisciplinary task force to create an evidence-based guideline for CNS GCTs. This guideline provides recommendations for multiple dimensions of clinical management for CNS GCTs, with particular focus on diagnostic measures including serum markers, treatment algorithms including surgery, radiotherapy, and chemotherapy, and under-investigated but important areas such as treatment for recurrent cases, long-term follow-up protocols, and long-term sequelae. This guideline serves the purpose of helping healthcare professionals keep up to date with current knowledge and standards of management for patients with this rare disease in daily clinical practice, as well as driving future translational and clinical research by recognizing unmet needs concerning this tumor.Entities:
Keywords: CNS germ cell tumor; diagnosis; guideline; prognosis; treatment
Mesh:
Year: 2022 PMID: 34671804 PMCID: PMC8972225 DOI: 10.1093/neuonc/noab242
Source DB: PubMed Journal: Neuro Oncol ISSN: 1522-8517 Impact factor: 13.029