Immunohistochemical evaluation of O6-methylguanine DNA methyltransferase (MGMT) expression in 117 cases of glioblastoma

被引:18
|
作者
Miyazaki, Masaya [1 ]
Nishihara, Hiroshi [2 ,9 ]
Terasaka, Shunsuke [3 ]
Kobayashi, Hiroyuki [3 ]
Yamaguchi, Shigeru [3 ]
Ito, Tamio [4 ]
Kamoshima, Yuuta [5 ]
Fujimoto, Shin [6 ]
Kaneko, Sadao [6 ]
Katoh, Masahito [7 ]
Ishii, Nobuaki [8 ]
Mohri, Hiromi [9 ]
Tanino, Mishie [1 ]
Kimura, Taichi [1 ]
Tanaka, Shinya [1 ,2 ]
机构
[1] Hokkaido Univ, Dept Canc Pathol, Grad Sch Med, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Dept Translat Pathol, Grad Sch Med, Sapporo, Hokkaido 0608638, Japan
[3] Hokkaido Univ, Dept Neurosurg, Grad Sch Med, Sapporo, Hokkaido 0608638, Japan
[4] Nakamura Mem Hosp, Sapporo, Hokkaido, Japan
[5] Sapporo Azabu Neurosurg Hosp, Sapporo, Hokkaido, Japan
[6] Kashiwaba Neurosurg Hosp, Sapporo, Hokkaido, Japan
[7] Hokkaido Neurosurg Mem Hosp, Sapporo, Hokkaido, Japan
[8] Keiwakai Ebetsu Hosp, Ebetsu, Hokkaido, Japan
[9] Hokuto Hosp, Lab Oncol, Obihiro, Hokkaido, Japan
关键词
glioblastoma; immunohistochemistry; MGMT; survival analysis; temozolomide; PROMOTER METHYLATION; PROTEIN EXPRESSION; O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE; PROGNOSTIC-SIGNIFICANCE; ADJUVANT TEMOZOLOMIDE; MALIGNANT GLIOMA; MISMATCH REPAIR; SURVIVAL; RADIOTHERAPY; CONCOMITANT;
D O I
10.1111/neup.12091
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Temozolomide (TMZ) is an oral alkylating agent which is widely used in the treatment of glioblastoma (GBM) and is composed of astrocytic and/or oligodendroglial tumors, and the evaluation of O6-methylguanine DNA methyltransferase (MGMT) expression is important to predict the response to TMZ therapy. In this study, we conducted immunohistochemical analysis of 117 cases of Japanese GBM including 19 cases of GBM with oligodendroglioma component (GBMO), using a scoring system for quantitative evaluation of staining intensity and proportion of MGMT, and performed survival analysis of these patients. Immunohistochemically, 55 cases (47%) were positive for MGMT with various intensities and proportions (total score (TS)2), while 62 cases (53%) were negative (TS=0). The distribution of MGMT expression pattern was not affected by any clinicopathological parameters such as the histological subtype (GBM vs. GBMO), age and gender. The survival analysis of these patients revealed that the minimal expression of MGMT (TS2) was a significant unfavorable prognostic factor (P<0.001) as well as resectability (P=0.004). Moreover, multivariate analysis showed that minimal MGMT expression in GBM was the most potent independent predictor for progression free survival (P<0.001) and also overall patient survival (P<0.001). This is the first report employing the scoring system for both staining intensity and proportion to evaluate immunohistochemical MGMT expression in GBM. In addition, our results emphases the clinicopathological values of the immunohistochemical approach for MGMT expression in glioma patients as a routine laboratory examination.
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页码:268 / 276
页数:9
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