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Status: Bibliographieeintrag

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Verfasst von:Ryba, Alice [VerfasserIn]   i
 Özdemir, Zeynep [VerfasserIn]   i
 Nissimov, Nitzan [VerfasserIn]   i
 Hönikl, Lisa [VerfasserIn]   i
 Neidert, Nicolas [VerfasserIn]   i
 Jakobs, Martin [VerfasserIn]   i
 Kalasauskas, Darius [VerfasserIn]   i
 Krigers, Aleksandrs [VerfasserIn]   i
 Thomé, Claudius [VerfasserIn]   i
 Freyschlag, Christian F [VerfasserIn]   i
 Ringel, Florian [VerfasserIn]   i
 Unterberg, Andreas [VerfasserIn]   i
 Dao Trong, Huy Philip [VerfasserIn]   i
 Beck, Jürgen [VerfasserIn]   i
 Heiland, Dieter Henrik [VerfasserIn]   i
 Meyer, Bernhard [VerfasserIn]   i
 Vajkoczy, Peter [VerfasserIn]   i
 Onken, Julia [VerfasserIn]   i
 Stummer, Walter [VerfasserIn]   i
 Suero Molina, Eric [VerfasserIn]   i
 Gempt, Jens [VerfasserIn]   i
 Westphal, Manfred [VerfasserIn]   i
 Schüller, Ulrich [VerfasserIn]   i
 Mohme, Malte [VerfasserIn]   i
Titel:Insights from a multicenter study on adult H3 K27M-mutated glioma
Titelzusatz:surgical resection’s limited influence on overall survival, ATRX as molecular prognosticator
Verf.angabe:Alice Ryba, Zeynep Özdemir, Nitzan Nissimov, Lisa Hönikl, Nicolas Neidert, Martin Jakobs, Darius Kalasauskas, Aleksandrs Krigers, Claudius Thomé, Christian F Freyschlag, Florian Ringel, Andreas Unterberg, Philip Dao Trong, Jürgen Beck, Dieter Henrik Heiland, Bernhard Meyer, Peter Vajkoczy, Julia Onken, Walter Stummer, Eric Suero Molina, Jens Gempt, Manfred Westphal, Ulrich Schüller, and Malte Mohme
E-Jahr:2024
Jahr:August 2024
Umfang:15 S.
Illustrationen:Illustrationen
Fussnoten:Veröffentlicht: 20 March 2024 ; Gesehen am 02.10.2024
Titel Quelle:Enthalten in: Neuro-Oncology
Ort Quelle:Oxford : Oxford Univ. Press, 1999
Jahr Quelle:2024
Band/Heft Quelle:26(2024), 8 vom: Aug., Seite 1479-1493
ISSN Quelle:1523-5866
Abstract:H3 K27M-mutated gliomas were first described as a new grade 4 entity in the 2016 World Health Organization classification. Current studies have focused on its typical appearance in children and young adults, increasing the need to better understand the prognostic factors and impact of surgery on adults. Here, we report a multicentric study of this entity in adults.We included molecularly confirmed H3 K27M-mutated glioma cases in patients ≥ 18 years diagnosed between 2016 and 2022. Clinical, radiological, and surgical features were analyzed. Univariate and multivariate analyses were performed to identify prognostic factors.Among 70 patients with a mean age of 36.1 years, the median overall survival (OS) was 13.6 ± 14 months. Gross-total resection was achieved in 14.3% of patients, whereas 30% had a subtotal resection and 54.3% a biopsy. Tumors located in telencephalon/diencephalon/myelencephalon were associated with a poorer OS, while a location in the mesencephalon/metencephalon showed a significantly longer OS (8.7 vs. 25.0 months, P = .007). Preoperative Karnofsky-Performance Score (KPS) ≤ 80 showed a reduced OS (4.2 vs. 18 months, P = .02). Furthermore, ATRX loss, found in 25.7%, was independently associated with an increased OS (31 vs. 8.3 months, P = .0029). Notably, patients undergoing resection showed no survival benefit over biopsy (12 vs. 11 months, P = .4006).The present study describes surgical features of H3 K27M-mutated glioma in adulthood in a large multicentric study. Our data reveal that ATRX status, location and KPS significantly impact OS in H3 K27M-mutated glioma. Importantly, our dataset indicates that resection does not offer a survival advantage over biopsy.
DOI:doi:10.1093/neuonc/noae061
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1093/neuonc/noae061
 DOI: https://doi.org/10.1093/neuonc/noae061
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1904186904
Verknüpfungen:→ Zeitschrift

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