Cargando…

Molecular features of glioblastomas in long-term survivors compared to short-term survivors—a matched-pair analysis

BACKGROUND: Although glioblastoma (GB) is associated with a devastating prognosis, a small proportion of patients achieve long-term survival rates. We herein present a matched-pair analysis of molecular factors found in long- and short-term survivors (LTS, STS). METHODS: We performed a cross-institu...

Descripción completa

Detalles Bibliográficos
Autores principales: Sommerlath, Vivien N., Buergy, Daniel, Etminan, Nima, Brehmer, Stefanie, Reuss, David, Sarria, Gustavo R., Guiot, Marie-Christin, Hänggi, Daniel, Wenz, Frederik, Petrecca, Kevin, Giordano, Frank A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785532/
https://www.ncbi.nlm.nih.gov/pubmed/35073955
http://dx.doi.org/10.1186/s13014-022-01984-w
Descripción
Sumario:BACKGROUND: Although glioblastoma (GB) is associated with a devastating prognosis, a small proportion of patients achieve long-term survival rates. We herein present a matched-pair analysis of molecular factors found in long- and short-term survivors (LTS, STS). METHODS: We performed a cross-institutional analysis of 262 patient records and matched a group of 91 LTS (≥ 3 years) with two groups of STS (STS-1, n = 91; STS-2, n = 80). Matching was performed according to age, Karnofsky Performance Status, initial therapy and adjuvant therapy. Molecular factors were compared between LTS (total of 91 patients) v. STS-1, and LTS (subgroup of 80 patients) v. STS-2. We included glial fibrillary acidic protein (GFAP), O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation, isocitrate dehydrogenase 1 (IDH-1); furthermore, the proliferation index was analyzed (Ki-67/MIB-1). RESULTS: IDH-1 and decreased Ki-67 were numerically associated with LTS but the difference was only significant compared to STS-1 (n.s. v. STS-2). LTS was associated with MGMT promoter hypermethylation (p = 0.013 and p = 0.022) and GFAP expression (p < 0.001 and p = 0.001). Positivity for both factors combined compared to negativity for one factor occurred more often in the LTS group (p = 0.002 and p = 0.006); negativity for both factors combined did not occur in the LTS group. CONCLUSION: In this retrospective analysis, GFAP expression and MGMT promoter methylation were associated with LTS. Given the hypothesis-generating nature of our study, these observations should be confirmed in prospective clinical trials. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13014-022-01984-w.