Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Mar;6(3):1719.
doi: 10.18103/mra.v6i3.1719. Epub 2018 Mar 15.

Primary Central Nervous System Germ Cell Tumors: A Review and Update

Affiliations

Primary Central Nervous System Germ Cell Tumors: A Review and Update

Kaleigh Fetcko et al. Med Res Arch. 2018 Mar.

Abstract

Importance: Primary central nervous system (CNS) germ cell tumors (GCT) are a heterogeneous group of tumors that are still poorly understood. In North America, GCTs comprise approximately 1% of primary brain tumors in pediatric and young adult patients. GCTs can occur as pure or mixed subtypes; they are divided into germinomas, which are the most common subtype, and non-germinomatous germ cell tumors (NGGCTs), which consist of approximately one-third of GCTs and include teratomas, embryonal carcinomas, choriocarcinomas, and yolk sac tumors.

Observations: While the etiology of primary CNS GCT is not entirely clear, the various subtypes are lineage-related and may involve progenitor germ cells that fail to migrate and become trapped in midline locations. Primary CNS GCT most commonly arises in the pineal region but also occur in other areas. Presenting symptoms can include headache, Parinaud syndrome, diabetes insipidus, precosious puberty, ataxia, or hemiparesis. Diagnosis of primary CNS GCTs can be difficult and is often delayed. Various imaging studies and tumor markers can assist in specific diagnosis. Treatment plans differ depending on the subtype of GCT and may vary among physicians and institutions. Germinomas have a favorable prognosis with a greater than 90% overall survival, while NGGCTs only have survival rates ranging from 40-70%.

Conclusions and relevance: Germinomas seem to be most effectively treated with chemotherapy and radiation, while NGGCT usually require surgical resection, chemotherapy, and radiation with the exception of mature teratomas frequently curable with surgery alone. Gamma knife radiosurgery is a promising treatment that may be an effective additional treatment option. Cytogenic and molecular analyses are attempting to further specify the different GCT subtypes and are helping to direct the development of distinct therapeutic targets to improve treatment and prognosis.

Keywords: CNS germ cell tumor; germinomas; intracranial germ cell tumor; nongerminomas.

PubMed Disclaimer

Conflict of interest statement

Disclosure Authors declare no conflict of interest.

References

    1. McCarthy BJ, Shibui S, Kayama T, et al. Primary CNS germ cell tumors in Japan and the United States: an analysis of 4 tumor registries. Neuro-oncology. 2012;14(9):1194–1200. - PMC - PubMed
    1. Goodwin TL, Sainani K, Fisher PG. Incidence patterns of central nervous system germ cell tumors: a SEER Study. Journal of pediatric hematology/oncology. 2009;31(8):541–544. - PubMed
    1. Murray MJ, Bartels U, Nishikawa R, Fangusaro J, Matsutani M, Nicholson JC. Consensus on the management of intracranial germ-cell tumours. The Lancet. Oncology. 2015;16(9):e470–e477. - PubMed
    1. Al-Hussaini M, Sultan I, Abuirmileh N, Jaradat I, Qaddoumi I. Pineal gland tumors: experience from the SEER database. Journal of neuro-oncology. 2009;94(3):351–358. - PMC - PubMed
    1. Bohrnsen F, Enders C, Ludwig HC, Bruck W, Fuzesi L, Gutenberg A. Common molecularcytogenetic alterations in tumors originating from the pineal region. Oncology letters. 2015;10(3):1853–1857. - PMC - PubMed

LinkOut - more resources