Comparative assessment of 5 methods (methylation-specific polymerase chain reaction, methylight, pyrosequencing, methylation-sensitive high-resolution melting, and immunohistochemistry) to analyze O6-methylguanine-DNA-methyltranferase in a series of 100 glioblastoma patients

被引:167
作者
Quillien, Veronique [1 ,2 ]
Lavenu, Audrey [3 ]
Karayan-Tapon, Lucie [4 ,5 ]
Carpentier, Catherine [6 ]
Labussiere, Marianne [6 ]
Lesimple, Thierry
Chinot, Olivier [7 ,8 ]
Wager, Michel [4 ]
Honnorat, Jerome [9 ,10 ]
Saikali, Stephan
Fina, Frederic [11 ]
Sanson, Marc [6 ]
Figarella-Branger, Dominique [7 ,8 ]
机构
[1] Ctr Eugene Marquis, Dept Biol, CS 44229, F-35042 Rennes, France
[2] Univ Rennes 1, CNRS, UMR6061, Rennes, France
[3] Univ Rennes 1, INSERM, CIC 0203, Rennes, France
[4] Univ Poitiers, INSERM, U935, Poitiers, France
[5] Univ Hosp Poitiers, Poitiers, France
[6] Univ Paris 06, INSERM, U975, CNRS,CRICM,UMR 7225,UMR S975, Paris, France
[7] Aix Marseille Univ, AP HM, CHU Timone, Neurooncol Team, Marseille, France
[8] Aix Marseille Univ, INSERM, U911, CRO2, Marseille, France
[9] Univ Lyon 1, Lyon Neurosci Res Ctr, INSERM, CNRS,UMR 5292,U1028, F-69372 Lyon, France
[10] Hosp Civils Lyon, Neurooncol Team, Neurol Hosp, Bron, France
[11] AP HM N Hosp, Oncol Transfert Lab, Marseille, France
关键词
glioblastoma; MGMT; promoter methylation; immunohistochemistry; survival; MGMT PROMOTER METHYLATION; NEWLY-DIAGNOSED GLIOBLASTOMA; O-6-METHYLGUANINE-DNA METHYLTRANSFERASE; PROGNOSTIC-SIGNIFICANCE; MALIGNANT GLIOMAS; EXPRESSION; SURVIVAL; DNA; TEMOZOLOMIDE; ASSOCIATION;
D O I
10.1002/cncr.27392
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: There is a strong need to determine the best technique for O6-methylguanine-DNA-methyltranferase (MGMT) analysis, because MGMT status is currently used in clinical trials and occasionally in routine clinical practice for glioblastoma patients. METHODS: The authors compared analytical performances and predictive values of 5 techniques in a series of 100 glioblastoma patients who received standard of care treatment (Stupp protocol). RESULTS: MGMT promoter was considered methylated in 33%, 33%, 42%, and 60% of patients by methylation-sensitive high-resolution melting, MethyLight, pyrosequencing (with an optimal risk cutoff at 8% for the average percentage of the 5 CpGs tested), and methylation-specific polymerase chain reaction (MS-PCR), respectively. Fifty-nine percent of the samples had <23% (the optimal risk cutoff) of MGMT-positive tumor cells. The best predictive values for overall survival (OS), after adjustment for age and performance status, were obtained by pyrosequencing (hazard ratio [HR], 0.32; P < .0001), MS-PCR (HR, 0.37; P < .0001), and immunohistochemistry (HR, 0.43; P = .0005) as compared with methylation-sensitive high-resolution melting (HR, 0.52 P = .02) and MethyLight (HR, 0.6; P = .05). For progression-free survival (PFS), the best predictive values were obtained with pyrosequencing (HR, 0.35; P < .0001), methylation-sensitive high-resolution melting (HR, 0.46; P = .002), and MS-PCR (HR, 0.49; P = .002). Combining pyrosequencing and immunohistochemistry slightly improved predictive power for OS, but not for PFS. Poor reproducibility and interobserver variability were, however, observed for immunohistochemistry. CONCLUSIONS: Good prediction of survival in addition to high reproducibility and sensitivity made pyrosequencing the best among the 5 techniques tested in this study. Cancer 2012. (c) 2012 American Cancer Society
引用
收藏
页码:4201 / 4211
页数:11
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