TY  - JOUR
AU  - Liu, Anthony P Y
AU  - Li, Bryan K
AU  - Vasiljevic, Alexandre
AU  - Dewan, Michael C
AU  - Tamrazi, Benita
AU  - Ertl-Wagner, Birgit
AU  - Hansford, Jordan R
AU  - Pfaff, Elke
AU  - Mynarek, Martin
AU  - Ng, Ho-Keung
AU  - Tsang, Derek S
AU  - Gottardo, Nicholas G
AU  - Gajjar, Amar
AU  - Bouffet, Eric
AU  - Dufour, Christelle
AU  - Pizer, Barry
AU  - Schiff, David
AU  - Jenkinson, Michael D
AU  - Lombardi, Giuseppe
AU  - Wen, Patrick Y
AU  - van den Bent, Martin J
AU  - Huang, Annie
TI  - SNO-EANO-EURACAN consensus on management of pineal parenchymal tumors.
JO  - Neuro-Oncology
VL  - 26
IS  - 12
SN  - 1522-8517
CY  - Oxford
PB  - Oxford Univ. Press
M1  - DKFZ-2024-01546
SP  - 2159-2173
PY  - 2024
N1  - 2024 Dec 5;26(12):2159-2173
AB  - Pineal parenchymal tumors are rare neoplasms for which evidence-based treatment recommendations are lacking. These tumors vary in biology, clinical characteristics, and prognosis, requiring treatment that ranges from surgical resection alone to intensive multimodal antineoplastic therapy. Recently, international collaborative studies have shed light on the genomic landscape of these tumors, leading to refinement in molecular-based disease classification in the 5th edition of the World Health Organization (WHO) classification of tumors of the central nervous system. In this review, we summarize the literature on diagnostic and therapeutic approaches, and suggest pragmatic recommendations for the clinical management of patients presenting with intrinsic pineal region masses including parenchymal tumors (pineocytoma, pineal parenchymal tumor of intermediate differentiation, and pineoblastoma), pineal cyst, and papillary tumors of the pineal region.
KW  - clinical treatment guidelines (Other)
KW  - papillary tumor of pineal region (Other)
KW  - pineal cyst (Other)
KW  - pineal parenchymal tumors (Other)
KW  - risk-stratification (Other)
LB  - PUB:(DE-HGF)16
C6  - pmid:39073785
DO  - DOI:10.1093/neuonc/noae128
UR  - https://inrepo02.dkfz.de/record/291934
ER  -