Open Access

Prognostic significance of IDH-1 and MGMT in patients with glioblastoma: One step forward, and one step back?

  • Stephanie E Combs1Email author,
  • Stefan Rieken1,
  • Wolfgang Wick2,
  • Amir Abdollahi1,
  • Andreas von Deimling3, 4,
  • Jürgen Debus1 and
  • Christian Hartmann3, 4
Radiation Oncology20116:115

DOI: 10.1186/1748-717X-6-115

Received: 2 April 2011

Accepted: 13 September 2011

Published: 13 September 2011

Abstract

A group of 160 patients with primary glioblastoma treated with radiotherapy and temozolomide was analyzed for the impact of O6-methly-guanly-methyl-transferase (MGMT)-promoter methylation as well as isocitrate dehydrogenase (IDH)1-mutational status. Unexpectedly, overall survival or progression-free survival were not longer in the group with methylated MGMT-promoter as compared to patients without that methylation. IDH-1 mutations were significantly associated with increased overall survival.

Keywords

Glioblastoma radiation temozolomide MGMT IDH

Introduction

Over recent years, the search for outcome factors in patients with glioblastomas (GBM) has identified at least two candidates that have shown to be prognostic for progression-free and overall survival or predictive for response to a particular therapeutic modality, that is alkylating chemotherapy, in patients with high-grade gliomas. The O6-methylguanine-DNA-methyltransferase (MGMT) gene encodes MGMT, a protein with DNA repair activity, which removes alkyl groups from several residues, of which the O6-position of guanine might be most relevant for the action of an extensively used chemotherapeutic drug, temozolomide, by an irreversible transfer of the alkyl group to a cystein residue at it's active side [1, 2]. The MGMT expression level and its activity varies widely between different tissues, cell types, and in particular, between different tumors [3, 4]. It has been shown that glial brain tumors are characterized by a low expression of MGMT, however, the activity of MGMT is commonly increased in relation to surrounding normal tissue [4, 5].

MGMT-activity is partly mediated through methylation of the MGMT promoter region; this epigenetic mechanism contributing to a loss of MGMT-expression has been described by Esteller et al. [6]. The epigenetically mediated silencing of the MGMT gene in GBM has been shown to correlate with an increased survival: Some studies have shown significant correlation with MGMT-promoter methylation and outcome to alkylating chemotherapeutic substances such as temozolomide (TMZ) [7]. Moreover, a correlation with outcome independently of treatment choice, i.e. chemotherapy or radiotherapy, has been postulated by some authors [7, 8].

However, until now, most reports on the prognostic value of MGMT-promoter methylation have answered this question in a retrospective manner. Additionally, several methods of MGMT-promoter methylation confirmation have been used within the different studies, and comparative analyses have shown substantial heterogeneity in results after MGMT-testing. In the literature, some authors have reported that MGMT promoter methylation might not be correlated with outcome, either after treatment with radiotherapy, or with alkylating chemotherapeutic substances [9, 10].

Only recently, mutations of the IDH1 gene encoding cytosolic NADP+-dependent isocitrate dehydrogenase have been show to correlate with outcome in patients with malignant gliomas [11, 12]. It has been proposed that IDH1 mutations can be used to distinguish primary from secondary GBM, since IDH1 mutations are associated with diffuse gliomas WHO Grade II and III as well as with secondary GBM, whereas primary GBM rarely show IDH1 mutations.

We have treated a large group of patients with primary GBM with radiotherapy and chemotherapy with temozolomide. To determine the prognostic value of MGMT-promoter methylation and IDH1 mutational status, we analyzed both markers in a homogenous group of 160 patients with primary GBM treated with radiation and TMZ and correlated results with outcome.

Materials and methods

Patient population

Between 1999 and 2007, 160 consecutive patients with primary, histologically confirmed GBM were treated with radiation and temozolomide as reported previously [13, 14].

After neurosurgical resection, which was complete in 51 patients and subtotal in 66 patients, patients were treated with 3D-conformal radiation therapy based on CT- and MRI-based treatment planning. The median age of the patients included was 56 years at primary diagnosis (range 20-76 months). Patients' characteristics are shown in table 1.
Table 1

Patients' characteristics of 160 patients treated with radiation and temozolomide for primary glioblastoma.

Characteristic

N (%)

Age - years

 

median

56

range

20-76

Age - no. (%)

 

< 50

38 (24)

≥ 50

122 (76)

Sex - number (%)

 

female

66 (41)

male

94 (59)

Karnofsky Performance Score

 

≥ 70

115 (72)

< 70

45 (28)

Extent of surgery - no. (%)

 

biopsy

43 (27)

complete resection

51 (32)

partial resection

66 (41)

RPA/EORTC-Classification

 

III

33 (21)

IV

90 (56)

V

37 (23)

Time from diagnosis to RT - days

 

median

24

range

7-98

Corticosteroid therapy - no. (%)

 

yes

113 (71)

no

47 (29)

Anti-seizure medication - no. (%)

 

yes

75 (47)

no

85 (53)

A median dose of 60 Gy in 2 Gy single fractions was applied. All patients were treated with concomitant TMZ, and adjuvant TMZ was given in 34 patients. At this time, a phase II trial evaluation radiation and chemotherapy with TMZ at a dose of 50 mg/m2 without adjuvant TMZ was performed in our institution, therefore 124 patients had been treated according to this regimen, and 36 patients received TMZ according to the Stupp regimen [13, 15, 16]. A detailed report on patient and treatment characteristics has been published previously [14].

Molecular analyses and immunohistochemistry

Tumor tissue for molecular analysis of MGMT-promoter methylation was available from 127 out of 160 patients (80%). MGMT status was determined using methylation-specific polymerase chain reaction [6]. Details are described elsewhere [17].

To determine the IDH1-mutational status we used either immunohistochemistry with an antibody specifically binding the R132H mutational variant of IDH1 (n = 125) or direct sequencing (n = 15). To determine the IDH1 status by immunohistochemistry, sections were cut to 4 μm, dried at 80°C for 15 min and further processed on a Ventana BenchMark XT immunostainer (Ventana Medical Systems, Tucson, AZ, USA). After 60 min pretreatment with cell conditioner 2 (pH 6) the slides were incubated with 1:30 diluted H09 antibody (Dianova, Hamburg, Germany) at 37°C for 32 min. Antibody incubation was followed by Ventana standard signal amplification, UltraWash, counterstaining with one drop of hematoxylin for 4 min and one drop of bluing reagent for 4 min. For chromogenic detection UltraViewTMUniversal DAB Detection Kit (Ventana) was used. Slides were removed from the immunostainer and mounted. A strong cytoplasmic immunoreaction product was scored positive. A weak diffuse staining and staining of macrophages were not scored positive. Figure 1 depicts an example of the immunohistochemistry as well as sequencing results.
Figure 1

GBM sample with an IDH1 R132H mutation demonstrated by IHC and sequencing.

Statistical Analysis

All patients were seen for regular follow-up and clinical data was collected in the institutions's database. For the present analysis, we correlated status of MGMT-promoter methylation as well as IDH-1 mutational status with patients' characteristics and outcome.

Overall survival (OS) was calculated from the date of primary diagnosis until death or last observation during follow up (censored data). Progression-free survival (PFS) was determined from the time of the beginning of radiotherapy and chemotherapy until tumor progression or to last observation or death if none occurred (censored data). OS and PFS were calculated using the Kaplan-Meier-Method. Survival curves for prognostic factors were compared using a two-sided log rank test. All statistical analyses were performed using the Statistica 6.1 software (Statsoft, Tulsa, OK, USA).

Results

Molecular analyses: MGMT Promoter Methylation

Of the 127 patients analyzed, the MGMT-promoter was methylated in 43 patients (34%) and was unmethylated in 84 patients (66%).

MGMT-promoter methylation did not correlate with overall survival (OS; p = 0.18 (Figure 2A)). Additionally progression-free-survival was not influenced by MGMT-promoter methylation status (p = 0.93; Figure 2B).
Figure 2

Correlation of overall survival (A) and progression-free survival (B) with MGMT-promotor methylation. For both endpoints, MGMT-activity did not significantly influence outcome.

Looking at subgroups, we analyzed the impact of MGMT- promoter methylation on OS and PFS in patients ≤ 60 yrs. (n = 85; 53%) and > 60 yrs. (n = 75; 47%). In the younger age group MGMT-promoter methylation did not influence OS (p = 0.93) or PFS (p = 0.69). However, in older patients, MGMT-promoter methylation was associated with a significant increase in OS (p = 0.02), however PFS was comparable (p = 0.11).

Molecular analyses and immunohistochemistry: IDH1

Four of the 140 patients (3%) showed an IDH1 mutation; all mutations were of the R132H variant. The 4 patients with a positive IDH1 mutations status showed significantly longer OS (p = 0.002; Figure 3A), but unaltered PFS (p = 0.25) than patients with wildtype IDH1.
Figure 3

IDH-1 mutational status did influcence overall survival in 160 patients treated with radiation and temozolomide (p = 0.002).

Discussion

In the present analysis we evaluated the impact of MGMT-promother methylation as well as IDH1-mutational status on outcome in 160 patients with GBM treated with radiation and temozolomide. IDH1 mutations occur in approximately 60 - 80% of diffusely infiltrating gliomas of the WHO grades II and III and in secondary GBM but only in around 5% of primary GBM [11, 1822]. In our series we identified in 4 of 140 patients (3%) IDH-1 mutations. Currently, it remains unclear if at least some of the patients with clinically defined primary GBM and IDH1 mutations may actually have suffered from secondary GBM that rapidly progressed from less malignant precursor lesions that escaped diagnosis [23]. In summary, IDH1 is a sufficient marker that allows a better separation of primary GBM from other malignant astrocytomas than any other marker and will help to define more accurately this tumor entity in upcoming studies. The low number of primary GBM exhibiting IDH1 mutations in our series indicates that our sample set consists indeed predominately of these tumors. IDH1 mutations in GBM were found in general in younger patients and were associated with a better prognosis [2224]. This has been confirmed in the present study, showing that IDH1 mutational status, although only positive in few patients, is associated with younger age and lower survival times than in the group of patients with wildtype IDH1. Therefore, the pattern of IDH1 mutations confirm that the present group of 160 patients with GBM is a very homogeneous group with respect to histological clasification.

In contrast to most studies, MGMT-promoter methylation was not associated with an increase in OS or PFS; both endpoints were comparable in patients with active MGMT or with MGMT silencing. The only subgroup of patients showing a significant impact of MGMT-promoter methylation on survival were patients older than 60 years, where MGMT-promoter methylation was associated with an increase in OS. This is in contrary to the results published by Stupp and colleagues [7, 15]. Therefore, the strong impact on MGMT-promoter methylation might not hold true for all age groups of patients with GBM. The EORTC 26981/22981/NCIC CE.3 study by Stupp et al. determining the role for chemoradiation with temozolomide has shown MGMT-promoter methylation to be strongly associated with an improved outcome [7, 15]. In contrast, other studies in anaplastic gliomas have shown that MGMT-methylation status dose not only influence outcome after alkylkating chemotherapies but also radiotherapy and may therefore be prognostic rather than predictive. This is reported by numerous other studies [8]. However, controversial results have also been published in groups of GBM patients, in which MGMT-status is not associated with differences in outcome: Costa et al. reports on 90 GBM-patients treated with temozolomide-based chemoradiation where MGMT promoter methylation was not associated with increased outcome [10]. Park et al. published 48 patients treated with alkylating chemotherapy and could not confirm a significant impact of methylation status of MGMT gene promoter [9]. Many arguments may be brought forward to explain these differing clinical data, including the various methods of measurement of MGMT-activity sometimes showing discrepant results, differences between frozen or paraffin embedded tissues. Additionally, when analyzing different chemotherapeutic combinations, substances such as cisplatinum might inactivate or attenuate MGMT-status thus influencing the clinical outcome when combined with alkylating chemotherapies. An important differential explanation is the variation of the treatment in our cohort as compared to the published data [7, 16, 17, 25, 26] with a lower exposure of our patients to alkylating chemotherapy both in the concomitant phase (50 mg in 78% and 75 mg in only 22%) as well as in the maintenance phase (no adjuvant treatment in 79% and a mean of 6 cycles in 21% of patients). However, inspite of this difference, outcome between the two dosing groups of temozolomide was identical, therefore counteracting this argument.

In conclusion, controversial results exist on the impact of MGMT-promoter methylation status in patients with GBM, and further studies will hopefully further clarify these differences. At this time, in spite of the strong evidence for a high impact of MGMT-promoter methylation, differentiating treatment strategies based on MGMT-promoter methylation status should therefore be applied within the framework of clinical studies only.

Conflict of interests

The authors declare that they have no competing interests.

Declarations

Authors’ Affiliations

(1)
Department of Radiation Oncology, University Hospital of Heidelberg
(2)
Department of Neurooncology, University Hospital of Heidelberg
(3)
Clinical Cooperation Unit Neuropathology, German Cancer Research Center
(4)
Department of Neuropathology, University Hospital of Heidelberg

References

  1. Pegg AE: Repair of O(6)-alkylguanine by alkyltransferases. Mutat Res 2000, 462: 83-100. 10.1016/S1383-5742(00)00017-XView ArticlePubMedGoogle Scholar
  2. Ludlum DB: DNA alkylation by the haloethylnitrosoureas: nature of modifications produced and their enzymatic repair or removal. Mutat Res 1990, 233: 117-26. 10.1016/0027-5107(90)90156-XView ArticlePubMedGoogle Scholar
  3. Margison GP, Povey AC, Kaina B, Santibanez Koref MF: Variability and regulation of O6-alkylguanine-DNA alkyltransferase. Carcinogenesis 2003, 24: 625-35. 10.1093/carcin/bgg005View ArticlePubMedGoogle Scholar
  4. Citron M, Decker R, Chen S, Schneider S, Graver M, Kleynerman L, et al.: O6-methylguanine-DNA methyltransferase in human normal and tumor tissue from brain, lung, and ovary. Cancer Res 1991, 51: 4131-4.PubMedGoogle Scholar
  5. Silber JR, Mueller BA, Ewers TG, Berger MS: Comparison of O6-methylguanine-DNA methyltransferase activity in brain tumors and adjacent normal brain. Cancer Res 1993, 53: 3416-20.PubMedGoogle Scholar
  6. Esteller M, Hamilton SR, Burger PC, Baylin SB, Herman JG: Inactivation of the DNA repair gene O6-methylguanine-DNA methyltransferase by promoter hypermethylation is a common event in primary human neoplasia. Cancer Res 1999, 59: 793-7.PubMedGoogle Scholar
  7. Hegi ME, Diserens AC, Gorlia T, Hamou MF, de Tribolet N, Weller M, et al.: MGMT gene silencing and benefit from temozolomide in glioblastoma. N Engl J Med 2005, 352: 997-1003. 10.1056/NEJMoa043331View ArticlePubMedGoogle Scholar
  8. Wick W, Hartmann C, Engel C, Stoffels M, Felsberg J, Stockhammer F, et al.: NOA-04 randomized phase III trial of sequential radiochemotherapy of anaplastic glioma with procarbazine, lomustine, and vincristine or temozolomide. J Clin Oncol 2009, 27: 5874-80. 10.1200/JCO.2009.23.6497View ArticlePubMedGoogle Scholar
  9. Park CK, Park SH, Lee SH, Kim CY, Kim DW, Paek SH, et al.: Methylation status of the MGMT gene promoter fails to predict the clinical outcome of glioblastoma patients treated with ACNU plus cisplatin. Neuropathology 2009, 29: 443-9. 10.1111/j.1440-1789.2008.00998.xView ArticlePubMedGoogle Scholar
  10. Costa BM, Caeiro C, Guimaraes I, Martinho O, Jaraquemada T, Augusto I, et al.: Prognostic value of MGMT promoter methylation in glioblastoma patients treated with temozolomide-based chemoradiation: a Portuguese multicentre study. Oncol Rep 2010, 23: 1655-62.PubMedGoogle Scholar
  11. Hartmann C, Meyer J, Balss J, Capper D, Mueller W, Christians A, et al.: Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: a study of 1,010 diffuse gliomas. Acta Neuropathol 2009, 118: 469-74. 10.1007/s00401-009-0561-9View ArticlePubMedGoogle Scholar
  12. Capper D, Weissert S, Balss J, Habel A, Meyer J, Jager D, et al.: Characterization of R132H mutation-specific IDH1 antibody binding in brain tumors. Brain Pathol 2010, 20: 245-54. 10.1111/j.1750-3639.2009.00352.xView ArticlePubMedGoogle Scholar
  13. Combs SE, Gutwein S, Schulz-Ertner D, van Kampen M, Thilmann C, Edler L, et al.: Temozolomide combined with irradiation as postoperative treatment of primary glioblastoma multiforme. Phase I/II study. Strahlenther Onkol 2005, 181: 372-7. 10.1007/s00066-005-1359-xView ArticlePubMedGoogle Scholar
  14. Combs SE, Wagner J, Bischof M, Welzel T, Edler L, Rausch R, et al.: Radiochemotherapy in patients with primary glioblastoma comparing two temozolomide dose regimens. Int J Radiat Oncol Biol Phys 2008, 71: 999-1005. 10.1016/j.ijrobp.2007.11.064View ArticlePubMedGoogle Scholar
  15. Stupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, Taphoorn MJ, et al.: Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med 2005, 352: 987-96. 10.1056/NEJMoa043330View ArticlePubMedGoogle Scholar
  16. Stupp R, Hegi ME, Mason WP, van den Bent MJ, Taphoorn MJ, Janzer RC, et al.: Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. Lancet Oncol 2009, 10: 459-66. 10.1016/S1470-2045(09)70025-7View ArticlePubMedGoogle Scholar
  17. Weiler M, Hartmann C, Wiewrodt D, Herrlinger U, Gorlia T, Bahr O, et al.: Chemoradiotherapy of newly diagnosed glioblastoma with intensified temozolomide. Int J Radiat Oncol Biol Phys 2010, 77: 670-6. 10.1016/j.ijrobp.2009.05.031View ArticlePubMedGoogle Scholar
  18. Balss J, Meyer J, Mueller W, Korshunov A, Hartmann C, von Deimling A: Analysis of the IDH1 codon 132 mutation in brain tumors. Acta Neuropathol 2008, 116: 597-602. 10.1007/s00401-008-0455-2View ArticlePubMedGoogle Scholar
  19. Ichimura K, Pearson DM, Kocialkowski S, Backlund LM, Chan R, Jones DT, et al.: IDH1 mutations are present in the majority of common adult gliomas but rare in primary glioblastomas. Neuro Oncol 2009, 11: 341-7. 10.1215/15228517-2009-025PubMed CentralView ArticlePubMedGoogle Scholar
  20. Parsons DW, Jones S, Zhang X, Lin JC, Leary RJ, Angenendt P, et al.: An integrated genomic analysis of human glioblastoma multiforme. Science 2008, 321: 1807-12. 10.1126/science.1164382PubMed CentralView ArticlePubMedGoogle Scholar
  21. Watanabe T, Nobusawa S, Kleihues P, Ohgaki H: IDH1 mutations are early events in the development of astrocytomas and oligodendrogliomas. Am J Pathol 2009, 174: 1149-53. 10.2353/ajpath.2009.080958PubMed CentralView ArticlePubMedGoogle Scholar
  22. Yan H, Parsons DW, Jin G, McLendon R, Rasheed BA, Yuan W, et al.: IDH1 and IDH2 mutations in gliomas. N Engl J Med 2009, 360: 765-73. 10.1056/NEJMoa0808710PubMed CentralView ArticlePubMedGoogle Scholar
  23. Nobusawa S, Watanabe T, Kleihues P, Ohgaki H: IDH1 mutations as molecular signature and predictive factor of secondary glioblastomas. Clin Cancer Res 2009, 15: 6002-7. 10.1158/1078-0432.CCR-09-0715View ArticlePubMedGoogle Scholar
  24. Sanson M, Marie Y, Paris S, Idbaih A, Laffaire J, Ducray F, et al.: Isocitrate dehydrogenase 1 codon 132 mutation is an important prognostic biomarker in gliomas. J Clin Oncol 2009, 27: 4150-4. 10.1200/JCO.2009.21.9832View ArticlePubMedGoogle Scholar
  25. Glas M, Happold C, Rieger J, Wiewrodt D, Bahr O, Steinbach JP, et al.: Long-term survival of patients with glioblastoma treated with radiotherapy and lomustine plus temozolomide. J Clin Oncol 2009, 27: 1257-61. 10.1200/JCO.2008.19.2195View ArticlePubMedGoogle Scholar
  26. Herrlinger U, Rieger J, Koch D, Loeser S, Blaschke B, Kortmann RD, et al.: Phase II trial of lomustine plus temozolomide chemotherapy in addition to radiotherapy in newly diagnosed glioblastoma: UKT-03. J Clin Oncol 2006, 24: 4412-7. 10.1200/JCO.2006.06.9104View ArticlePubMedGoogle Scholar

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© Combs et al; licensee BioMed Central Ltd. 2011

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