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@ARTICLE{Liu:291934,
      author       = {A. P. Y. Liu and B. K. Li and A. Vasiljevic and M. C. Dewan
                      and B. Tamrazi and B. Ertl-Wagner and J. R. Hansford and E.
                      Pfaff$^*$ and M. Mynarek and H.-K. Ng and D. S. Tsang and N.
                      G. Gottardo and A. Gajjar and E. Bouffet and C. Dufour and
                      B. Pizer and D. Schiff and M. D. Jenkinson and G. Lombardi
                      and P. Y. Wen and M. J. van den Bent and A. Huang},
      title        = {{SNO}-{EANO}-{EURACAN} consensus on management of pineal
                      parenchymal tumors.},
      journal      = {Neuro-Oncology},
      volume       = {26},
      number       = {12},
      issn         = {1522-8517},
      address      = {Oxford},
      publisher    = {Oxford Univ. Press},
      reportid     = {DKFZ-2024-01546},
      pages        = {2159-2173},
      year         = {2024},
      note         = {2024 Dec 5;26(12):2159-2173},
      abstract     = {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.},
      subtyp        = {Review Article},
      keywords     = {clinical treatment guidelines (Other) / papillary tumor of
                      pineal region (Other) / pineal cyst (Other) / pineal
                      parenchymal tumors (Other) / risk-stratification (Other)},
      cin          = {B360},
      ddc          = {610},
      cid          = {I:(DE-He78)B360-20160331},
      pnm          = {312 - Funktionelle und strukturelle Genomforschung
                      (POF4-312)},
      pid          = {G:(DE-HGF)POF4-312},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:39073785},
      doi          = {10.1093/neuonc/noae128},
      url          = {https://inrepo02.dkfz.de/record/291934},
}