TY - JOUR
T1 - Long-term survivors of glioblastoma
T2 - Clinical features and molecular analysis
AU - Sonoda, Yukihiko
AU - Kumabe, Toshihiro
AU - Watanabe, Mika
AU - Nakazato, Yoichi
AU - Inoue, Tomoo
AU - Kanamori, Masayuki
AU - Tominaga, Teiji
N1 - Funding Information:
This work was supported in part by Grants-in-Aid for Cancer Research from the Ministry of Health and Welfare in Japan to T.T. We thank Nippon Gene Research Laboratories Inc. for QRT-PCR and direct sequencing analysis.
PY - 2009/11
Y1 - 2009/11
N2 - Background: Glioblastoma is a highly lethal neoplasm with a median survival of 12-14 months; only 2-5% of patients survive >3 years. Methods: At our institute, patients with glioblastoma are initially treated with maximum tumor resection followed by radiation and the intravenous injection of nimustine hydrochloride (ACNU). Results: Using this strategy, 18 of 123 (14.6%) patients treated at our hospital survived >3 years; 7 manifested no recurrence, and the other 11 had early recurrence and received additional therapies. To identify factors associated with prolonged survival, we compared these patients with 21 short-term (<1.5 years) glioblastoma survivors. In the long-term survivors, the MGMT promoter methylation was significantly more frequent. The rate of p53 mutation was lower, and the rate of PTEN mutations and the proliferation index were slightly higher in short-term survivors. Conclusion: By multivariate analysis, we found that a younger age and MGMT promoter methylation were significant favorable factors in patients with glioblastoma.
AB - Background: Glioblastoma is a highly lethal neoplasm with a median survival of 12-14 months; only 2-5% of patients survive >3 years. Methods: At our institute, patients with glioblastoma are initially treated with maximum tumor resection followed by radiation and the intravenous injection of nimustine hydrochloride (ACNU). Results: Using this strategy, 18 of 123 (14.6%) patients treated at our hospital survived >3 years; 7 manifested no recurrence, and the other 11 had early recurrence and received additional therapies. To identify factors associated with prolonged survival, we compared these patients with 21 short-term (<1.5 years) glioblastoma survivors. In the long-term survivors, the MGMT promoter methylation was significantly more frequent. The rate of p53 mutation was lower, and the rate of PTEN mutations and the proliferation index were slightly higher in short-term survivors. Conclusion: By multivariate analysis, we found that a younger age and MGMT promoter methylation were significant favorable factors in patients with glioblastoma.
KW - Glioblastoma
KW - Long-term survival
KW - MGMT
KW - P53
KW - PTEN
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U2 - 10.1007/s00701-009-0387-1
DO - 10.1007/s00701-009-0387-1
M3 - Article
C2 - 19730774
AN - SCOPUS:70449521966
SN - 0001-6268
VL - 151
SP - 1349
EP - 1358
JO - Acta Neurochirurgica
JF - Acta Neurochirurgica
IS - 11
ER -