SNO-EANO-EURACAN consensus on management of pineal parenchymal tumors

Anthony P.Y. Liu; Bryan K. Li; Alexandre Vasiljevic; Michael C. Dewan; Benita Tamrazi; Birgit Ertl-Wagner; Jordan R. Hansford; Elke Pfaff; Martin Mynarek; Ho Keung Ng; Derek S. Tsang; Nicholas G. Gottardo; Amar Gajjar; Eric Bouffet; Christelle Dufour; Barry Pizer; David Schiff; Michael D. Jenkinson; Giuseppe Lombardi; Patrick Y. Wen; Martin J. van den Bent; Annie Huang

doi:10.1093/neuonc/noae128

SNO-EANO-EURACAN consensus on management of pineal parenchymal tumors

Anthony P.Y. Liu, Bryan K. Li, Alexandre Vasiljevic, Michael C. Dewan, Benita Tamrazi, Birgit Ertl-Wagner, Jordan R. Hansford, Elke Pfaff, Martin Mynarek, Ho Keung Ng, Derek S. Tsang, Nicholas G. Gottardo, Amar Gajjar, Eric Bouffet, Christelle Dufour, Barry Pizer, David Schiff, Michael D. Jenkinson, Giuseppe Lombardi, Patrick Y. WenMartin J. van den Bent, Annie Huang

Résultats de recherche: Contribution à un journal › Article 'review' › Revue par des pairs

Résumé

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.

langue originale	Anglais
Pages (de - à)	2159-2173
Nombre de pages	15
journal	Neuro-Oncology
Volume	26
Numéro de publication	12
Les DOIs	https://doi.org/10.1093/neuonc/noae128
état	Publié - 1 déc. 2024

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10.1093/neuonc/noae128

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Contient cette citation

Liu, A. P. Y., Li, B. K., Vasiljevic, A., Dewan, M. C., Tamrazi, B., Ertl-Wagner, B., Hansford, J. R., Pfaff, E., Mynarek, M., Ng, H. K., Tsang, D. S., Gottardo, N. G., Gajjar, A., Bouffet, E., Dufour, C., Pizer, B., Schiff, D., Jenkinson, M. D., Lombardi, G., ... Huang, A. (2024). SNO-EANO-EURACAN consensus on management of pineal parenchymal tumors. Neuro-Oncology, 26(12), 2159-2173. https://doi.org/10.1093/neuonc/noae128

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title = "SNO-EANO-EURACAN consensus on management of pineal parenchymal tumors",

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.",

keywords = "clinical treatment guidelines, papillary tumor of pineal region, pineal cyst, pineal parenchymal tumors, risk-stratification",

author = "Liu, {Anthony P.Y.} and Li, {Bryan K.} and Alexandre Vasiljevic and Dewan, {Michael C.} and Benita Tamrazi and Birgit Ertl-Wagner and Hansford, {Jordan R.} and Elke Pfaff and Martin Mynarek and Ng, {Ho Keung} and Tsang, {Derek S.} and Gottardo, {Nicholas G.} and Amar Gajjar and Eric Bouffet and Christelle Dufour and Barry Pizer and David Schiff and Jenkinson, {Michael D.} and Giuseppe Lombardi and Wen, {Patrick Y.} and {van den Bent}, {Martin J.} and Annie Huang",

year = "2024",

month = dec,

day = "1",

doi = "10.1093/neuonc/noae128",

language = "English",

volume = "26",

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journal = "Neuro-Oncology",

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Liu, APY, Li, BK, Vasiljevic, A, Dewan, MC, Tamrazi, B, Ertl-Wagner, B, Hansford, JR, Pfaff, E, Mynarek, M, Ng, HK, Tsang, DS, Gottardo, NG, Gajjar, A, Bouffet, E, Dufour, C, Pizer, B, Schiff, D, Jenkinson, MD, Lombardi, G, Wen, PY, van den Bent, MJ & Huang, A 2024, 'SNO-EANO-EURACAN consensus on management of pineal parenchymal tumors', Neuro-Oncology, VOL. 26, Numéro 12, p. 2159-2173. https://doi.org/10.1093/neuonc/noae128

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T1 - SNO-EANO-EURACAN consensus on management of pineal parenchymal tumors

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

PY - 2024/12/1

Y1 - 2024/12/1

N2 - 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.

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

KW - papillary tumor of pineal region

KW - pineal cyst

KW - pineal parenchymal tumors

KW - risk-stratification

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