TY - JOUR
T1 - Revisiting prognostic factors of gliomatosis cerebri in adult-type diffuse gliomas
AU - Shin, Ilah
AU - Sim, Yongsik
AU - Choi, Seo Hee
AU - Park, Yae Won
AU - Lee, Narae
AU - Ahn, Sung Soo
AU - Chang, Jong Hee
AU - Kim, Se Hoon
AU - Lee, Seung Koo
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024.
PY - 2024/6
Y1 - 2024/6
N2 - Purpose: There is lack of comprehensive analysis evaluating the impact of clinical, molecular, imaging, and surgical data on survival of patients with gliomatosis cerebri (GC). This study aimed to investigate prognostic factors of GC in adult-type diffuse glioma patients. Methods: Retrospective chart and imaging review was performed in 99 GC patients from adult-type diffuse glioma (among 1,211 patients; 6 oligodendroglioma, 16 IDH-mutant astrocytoma, and 77 IDH-wildtype glioblastoma) from a single institution between 2005 and 2021. Predictors of overall survival (OS) of entire patients and IDH-wildtype glioblastoma patients were determined. Results: The median OS was 16.7 months (95% confidence interval [CI] 14.2–22.2) in entire patients and 14.3 months (95% CI 12.2–61.9) in IDH-wildtype glioblastoma patients. In entire patients, KPS (hazard ratio [HR] = 0.98, P = 0.004), no 1p/19q codeletion (HR = 10.75, P = 0.019), MGMTp methylation (HR = 0.54, P = 0.028), and hemorrhage (HR = 3.45, P = 0.001) were independent prognostic factors on multivariable analysis. In IDH-wildtype glioblastoma patients, KPS (HR = 2.24, P = 0.075) was the only independent prognostic factor on multivariable analysis. In subgroup of IDH-wildtype glioblastoma with CE tumors, total resection of CE tumor did not remain as a significant prognostic factor (HR = 1.13, P = 0.685). Conclusions: The prognosis of GC patients is determined by its underlying molecular type and patient performance status. Compared with diffuse glioma without GC, aggressive surgery of CE tumor in GC patients does not improve survival.
AB - Purpose: There is lack of comprehensive analysis evaluating the impact of clinical, molecular, imaging, and surgical data on survival of patients with gliomatosis cerebri (GC). This study aimed to investigate prognostic factors of GC in adult-type diffuse glioma patients. Methods: Retrospective chart and imaging review was performed in 99 GC patients from adult-type diffuse glioma (among 1,211 patients; 6 oligodendroglioma, 16 IDH-mutant astrocytoma, and 77 IDH-wildtype glioblastoma) from a single institution between 2005 and 2021. Predictors of overall survival (OS) of entire patients and IDH-wildtype glioblastoma patients were determined. Results: The median OS was 16.7 months (95% confidence interval [CI] 14.2–22.2) in entire patients and 14.3 months (95% CI 12.2–61.9) in IDH-wildtype glioblastoma patients. In entire patients, KPS (hazard ratio [HR] = 0.98, P = 0.004), no 1p/19q codeletion (HR = 10.75, P = 0.019), MGMTp methylation (HR = 0.54, P = 0.028), and hemorrhage (HR = 3.45, P = 0.001) were independent prognostic factors on multivariable analysis. In IDH-wildtype glioblastoma patients, KPS (HR = 2.24, P = 0.075) was the only independent prognostic factor on multivariable analysis. In subgroup of IDH-wildtype glioblastoma with CE tumors, total resection of CE tumor did not remain as a significant prognostic factor (HR = 1.13, P = 0.685). Conclusions: The prognosis of GC patients is determined by its underlying molecular type and patient performance status. Compared with diffuse glioma without GC, aggressive surgery of CE tumor in GC patients does not improve survival.
KW - Glioma
KW - Gliomatosis cerebri
KW - Magnetic resonance imaging
KW - Survival
KW - World Health Organization
UR - http://www.scopus.com/inward/record.url?scp=85191961346&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85191961346&partnerID=8YFLogxK
U2 - 10.1007/s11060-024-04656-9
DO - 10.1007/s11060-024-04656-9
M3 - Article
C2 - 38700610
AN - SCOPUS:85191961346
SN - 0167-594X
VL - 168
SP - 239
EP - 247
JO - Journal of Neuro-Oncology
JF - Journal of Neuro-Oncology
IS - 2
ER -