Clinical, Therapeutic, and Prognostic Experience in Patients With Glioblastoma

Background: Glioblastoma (GB) represents the most aggressive type of glioma with a poor prognosis despite the therapies used. As of today, data availability for therapeutic and prognosis experiences is limited. The cornerstone for this study is to create a framework overview of Mexico´s experience t...

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Veröffentlicht in:Curēus (Palo Alto, CA) CA), 2022-10, Vol.14 (10), p.e29856-e29856
Hauptverfasser: Mondragon-Soto, Michel, Rodríguez-Hernández, Luis A, Moreno Jiménez, Sergio, Gómez Amador, Juan Luis, Gutierrez-Aceves, Axayacatl, Montano-Tello, Humberto, Reyes-Moreno, Ignacio, Santos-Zambrano, Jose, Castro-Martinez, Elvira, Gonzalez-Aguilar, Alberto
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Sprache:eng
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Zusammenfassung:Background: Glioblastoma (GB) represents the most aggressive type of glioma with a poor prognosis despite the therapies used. As of today, data availability for therapeutic and prognosis experiences is limited. The cornerstone for this study is to create a framework overview of Mexico´s experience throughout 17 years of research.Methods: Retrospective analysis from 2000 to 2017 including patients with a histological diagnosis of GB was performed. Data were collected from the ABC Medical Center and the Neurology and Neurosurgery National Institute.Results: One hundred and thirty-seven patients were included with a mean age of 54 years. Histological diagnosis was made in all patients, of which 58.1% had a total resection, 31.6% had a partial resection, and 10.3% of them underwent biopsy. In all cases, patients received treatment under the following conditions: 10 patients were treated exclusively with stereotactic radiotherapy (RT). In 55 patients, a combination of RT and TMZ was used, the other 40 patients received RT plus CBP. Eighteen patients RT added to nitrosourea medication and lastly, 14 patients received a combination of RT/TMZ and Bevacizumab, a monoclonal antibody that inhibits the formation of blood vessels (BVZ). The progression-free survival (PFS) and overall survival (OS) were higher in the RT/TMZ/BVZ group (16.5 to 22.9 months) and the RT/TMZ group (11 to 17 months), the prognostic parameters included: Isocitrate dehydrogenase 1 mutation (IDH1), usage of BVZ and TMZ in the PLS and OS, considering as well, age range (
ISSN:2168-8184
2168-8184
DOI:10.7759/cureus.29856