Long-term survivors in 976 supratentorial glioblastoma, IDH-wildtype patients

被引:2
作者
Aboubakr, Oumaima [1 ,2 ,3 ]
Moiraghi, Alessandro [1 ,2 ]
Elia, Angela [1 ,2 ]
Tauziede-Espariat, Arnault [3 ]
Roux, Alexandre [1 ,2 ]
Leclerc, Arthur [2 ,4 ,5 ]
Planet, Martin [1 ,2 ]
Bedioui, Aziz [1 ,2 ]
Simboli, Giorgia Antonia [1 ,2 ]
Dhermain, Frederic [6 ]
Parraga, Eduardo [1 ,2 ]
Benevello, Chiara [7 ]
Fathallah, Houssem [1 ,2 ]
Muto, Jun [8 ]
Chretien, Fabrice [1 ,3 ]
Dezamis, Edouard [1 ,2 ]
Oppenheim, Catherine [1 ,9 ]
Varlet, Pascale [1 ,3 ]
Zanello, Marc [1 ,2 ]
Pallud, Johan [1 ,2 ]
机构
[1] Univ Paris Cite, Inst Psychiat & Neurosci Paris IPNP, INSERM, Paris, France
[2] GHU Paris Psychiat & Neurosci, Dept Neurosurg, Paris, France
[3] GHU Paris Psychiat & Neurosci, Dept Neuropathol, Paris, France
[4] Caen Univ Hosp, Dept Neurosurg, Caen, France
[5] Normandy Univ, Unicaen, ISTCT, CERVOxy Grp,UMR6030,GIP CYCERON, Caen, France
[6] Gustave Roussy Univ Hosp, Dept Radiat Oncol, Canc Campus Grand Paris, Villejuif, France
[7] European Hosp Paris Roseraie, Dept Neurosurg, Aubervilliers, France
[8] Fujita Hlth Univ, Dept Neurosurg, Aichi, Aichi, Japan
[9] GHU Paris Psychiat & Neurosci, Dept Neuroradiol, Paris, France
关键词
glioblastoma; isocitrate dehydrogenase; overall survival; surgery; survival analysis; oncology; tumor; ADJUVANT TEMOZOLOMIDE; GLIOBLASTOMA; GLIOMAS; RADIOTHERAPY; CONCOMITANT; TUMORS;
D O I
10.3171/2024.5.JNS24393
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE Glioblastoma, isocitrate dehydrogenase (IDH)-wildtype is the most aggressive glioma with poor outcomes. The authors explored survival rates and factors associated with long-term survival in patients harboring a METHODS In an observational, retrospective, single-center study, the authors examined the medical records of 976 adults newly diagnosed with supratentorial glioblastomas, IDH-wildtype between January 2000 and January 2021. They analyzed clinical-, imaging-, and treatment-related factors associated with 2-year and 5-year survival. RESULTS The median overall survival was 11.2 months (12.2 months for patients included after 2005 and the introduction of standard combined chemoradiotherapy). The median progression-free survival was 9.4 months (10.0 months for patients included after 2005). Overall, 17.6% of patients reached a 2-year overall survival, while 2.2% of patients reached a 5-year overall survival. Furthermore, 6.6% of patients survived 2 years without progression, while 1.1% of patients survived 5 years without progression. Two factors that were consistently associated with 2-year and 5-year survival were first-line oncological treatment with standard combined chemoradiotherapy and methylated O6-methylguanineDNA methyltransferase promoter. Other factors that were significantly associated with 2-year or 5-year survival were age at diagnosis <= 60 years, headaches or signs of raised intracranial pressure at diagnosis, cortical contact of contrast enhancement, no contrast enhancement crossing the midline on initial imaging, total or subtotal tumor resection, and a second line of oncological treatment at recurrence. Within 21 cases of 5-year survival, 18 were confirmed to be glioblastomas, IDH-wildtype, and 7 of the 5-year survivors (38.9%) had additional genetic alterations: 3 cases had an FGFR mutation or fusion, 3 cases had a PIK3CA mutation, 1 case had a PTPN11 mutation, and 1 case had a PMS2 mutation in CONCLUSIONS Five-year overall survival in patients with glioblastoma, IDH-wildtype is extremely low. Predictors of a longer survival are mostly treatment factors, emphasizing the importance of a complete oncological treatment plan, when achievable. Glioblastoma, IDH-wildtype 5-year survivors could be screened for actionable targets in case of recurrence.
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收藏
页码:174 / 186
页数:13
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