Radiological features combined with IDH1 status for predicting the survival outcome of glioblastoma patients.

BACKGROUND Radiological characteristics may reflect the biological features of brain tumors and may be associated with genetic alterations that occur in tumorigenesis. This study aimed to investigate the relationship between radiological features and IDH1 status as well as their predictive value for survival of glioblastoma patients. METHODS The clinical information and MR images of 280 patients with histologically confirmed glioblastoma were retrospectively reviewed. The radiological characteristics of tumors were examined on MR images, and the IDH1 status was determined using DNA sequencing for all cases. The Kaplan-Meier method and Cox regression model were used to identify prognostic factors for progression-free and overall survival. RESULTS The IDH1 mutation was associated with longer progression-free survival (P = .022; hazard ratio, 0.602) and overall survival (P = .018; hazard ratio, 0.554). In patients with the IDH1 mutation, tumor contrast enhancement and peritumoral edema indicated worse progression-free survival (P = .015 and P = .024, respectively) and worse overall survival (P = .024 and P = .032, respectively). For tumors with contrast enhancement, multifocal contrast enhancement of the tumor lesion was associated with poor progression-free survival (P = .002) and poor overall survival (P = .010) in patients with wild-type IDH1 tumors. CONCLUSIONS Combining the radiological features and IDH1 status of a tumor allows more accurate prediction of survival outcomes in glioblastoma patients. The complementary roles of genetic changes and radiological features of tumors should be considered in future studies.

[1]  Y. Fujii,et al.  Immunohistochemical profiles of IDH1, MGMT and P53: Practical significance for prognostication of patients with diffuse gliomas , 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

[2]  T. Jiang,et al.  Genome-wide transcriptional analyses of Chinese patients reveal cell migration is attenuated in IDH1-mutant glioblastomas. , 2015, Cancer letters.

[3]  T. Jiang,et al.  IDH1/2 mutation is associated with seizure as an initial symptom in low-grade glioma: A report of 311 Chinese adult glioma patients , 2015, Epilepsy Research.

[4]  S. Artan,et al.  IDH1 mutations is prognostic marker for primary glioblastoma multiforme but MGMT hypermethylation is not prognostic for primary glioblastoma multiforme. , 2015, Gene.

[5]  S. Choi,et al.  Prognosis of Glioblastoma With Oligodendroglioma Component is Associated With the IDH1 Mutation and MGMT Methylation Status1 , 2014, Translational oncology.

[6]  Sibel Karaca,et al.  Comparison of linear accelerator and helical tomotherapy plans for glioblastoma multiforme patients. , 2014, Asian Pacific journal of cancer prevention : APJCP.

[7]  Pieter Wesseling,et al.  The combination of IDH1 mutations and MGMT methylation status predicts survival in glioblastoma better than either IDH1 or MGMT alone. , 2014, Neuro-oncology.

[8]  M. Chamberlain Prognostic or predictive value of MGMT promoter methylation in gliomas depends on IDH1 mutation , 2014, Neurology.

[9]  Caroline Dehais,et al.  Contrast enhancement in 1p/19q-codeleted anaplastic oligodendrogliomas is associated with 9p loss, genomic instability, and angiogenic gene expression. , 2014, Neuro-oncology.

[10]  R. Kaneva,et al.  IDH1/IDH2 but Not TP53 Mutations Predict Prognosis in Bulgarian Glioblastoma Patients , 2014, BioMed research international.

[11]  S. Qi,et al.  Isocitrate dehydrogenase mutation is associated with tumor location and magnetic resonance imaging characteristics in astrocytic neoplasms , 2014, Oncology letters.

[12]  K. Black,et al.  Cystic Glioblastoma : An Evaluation of IDH 1 Status and Prognosis , 2013 .

[13]  J. Uhm,et al.  Adult Low-grade Glioma: 19-year Experience at a Single Institution , 2013, American journal of clinical oncology.

[14]  G. Reifenberger,et al.  Prognostic or predictive value of MGMT promoter methylation in gliomas depends on IDH1 mutation , 2013, Neurology.

[15]  Zhi Wang,et al.  IDH1 mutation is associated with improved overall survival in patients with glioblastoma: a meta-analysis , 2013, Tumor Biology.

[16]  K. Aldape,et al.  Significance of complete 1p/19q co-deletion, IDH1 mutation and MGMT promoter methylation in gliomas: use with caution , 2013, Modern Pathology.

[17]  P. Gibbs,et al.  Clinical trial participation and outcome for patients with glioblastoma: Multivariate analysis from a comprehensive dataset , 2013, Journal of Clinical Neuroscience.

[18]  Zhe Zhang,et al.  Differential molecular genetic analysis in glioblastoma multiforme of long- and short-term survivors: a clinical study in Chinese patients , 2013, Journal of Neuro-Oncology.

[19]  D. Cahill,et al.  From genomics to the clinic: biological and translational insights of mutant IDH1/2 in glioma. , 2013, Neurosurgical focus.

[20]  T. Jiang,et al.  Correlation of IDH1/2 mutation with clinicopathologic factors and prognosis in anaplastic gliomas: a report of 203 patients from China , 2013, Journal of Cancer Research and Clinical Oncology.

[21]  S. Cha,et al.  Relationship of glioblastoma multiforme to the subventricular zone is associated with survival. , 2013, Neuro-oncology.

[22]  B. Neyns,et al.  Correlation of EGFR, IDH1 and PTEN status with the outcome of patients with recurrent glioblastoma treated in a phase II clinical trial with the EGFR-blocking monoclonal antibody cetuximab. , 2012, International Journal of Oncology.

[23]  T. Cloughesy,et al.  Relationship between Tumor Enhancement, Edema, IDH1 Mutational Status, MGMT Promoter Methylation, and Survival in Glioblastoma , 2012, American Journal of Neuroradiology.

[24]  Lei Wang,et al.  Correlation of IDH1 Mutation with Clinicopathologic Factors and Prognosis in Primary Glioblastoma: A Report of 118 Patients from China , 2012, PloS one.

[25]  Joel H. Saltz,et al.  Integrative, Multimodal Analysis of Glioblastoma Using TCGA Molecular Data, Pathology Images, and Clinical Outcomes , 2011, IEEE Transactions on Biomedical Engineering.

[26]  Vahid Afaghi,et al.  The impact of molecular and clinical factors on patient outcome in oligodendroglioma from 20years’ experience at a single centre , 2011, Journal of Clinical Neuroscience.

[27]  G. Reifenberger,et al.  Patients with IDH 1 wild type anaplastic astrocytomas exhibit worse prognosis than IDH 1-mutated glioblastomas , and IDH 1 mutation status accounts for the unfavorable prognostic effect of higher age : implications for classification of gliomas , 2010 .

[28]  R. Wilson,et al.  Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. , 2010, Cancer cell.

[29]  S. Gabriel,et al.  Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. , 2010, Cancer cell.

[30]  Ru-Fang Yeh,et al.  Glioblastoma multiforme regional genetic and cellular expression patterns: influence on anatomic and physiologic MR imaging. , 2010, Radiology.

[31]  R. McLendon,et al.  IDH1 and IDH2 mutations in gliomas. , 2009, The New England journal of medicine.

[32]  Xin-gang Li,et al.  Survival analysis of 205 patients with glioblastoma multiforme: Clinical characteristics, treatment and prognosis in China , 2009, Journal of Clinical Neuroscience.

[33]  Stanley F. Nelson,et al.  Stem cell associated gene expression in glioblastoma multiforme: relationship to survival and the subventricular zone , 2009, Journal of Neuro-Oncology.

[34]  Christian Mawrin,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 , 2009, Acta Neuropathologica.

[35]  A. Marchetti,et al.  IDH1 mutations at residue p.R132 (IDH1R132) occur frequently in high‐grade gliomas but not in other solid tumors , 2009, Human mutation.

[36]  Andrey Korshunov,et al.  Analysis of the IDH1 codon 132 mutation in brain tumors , 2008, Acta Neuropathologica.

[37]  S. Horvath,et al.  Gene expression analysis of glioblastomas identifies the major molecular basis for the prognostic benefit of younger age , 2008, BMC Medical Genomics.

[38]  Paul S Mischel,et al.  Relationship between gene expression and enhancement in glioblastoma multiforme: exploratory DNA microarray analysis. , 2008, Radiology.

[39]  K. Aldape,et al.  Identification of noninvasive imaging surrogates for brain tumor gene-expression modules , 2008, Proceedings of the National Academy of Sciences.

[40]  D. Reardon,et al.  Diagnosis and treatment of high-grade astrocytoma. , 2007, Neurologic clinics.

[41]  Catherine Dumur,et al.  Microarray Analysis of MRI-defined Tissue Samples in Glioblastoma Reveals Differences in Regional Expression of Therapeutic Targets , 2006, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

[42]  K. Fujii,et al.  Pathological and clinical features of cystic and noncystic glioblastomas , 2006, Brain Tumor Pathology.

[43]  Thomas D. Wu,et al.  Molecular subclasses of high-grade glioma predict prognosis, delineate a pattern of disease progression, and resemble stages in neurogenesis. , 2006, Cancer cell.

[44]  Paul S Mischel,et al.  MR imaging correlates of survival in patients with high-grade gliomas. , 2005, AJNR. American journal of neuroradiology.

[45]  Martin J. van den Bent,et al.  Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. , 2005, The New England journal of medicine.

[46]  Raymond Sawaya,et al.  Cystic glioblastoma multiforme: survival outcomes in 22 cases. , 2004, Journal of neurosurgery.

[47]  Raymond Sawaya,et al.  Prognostic significance of preoperative MRI scans in glioblastoma multiforme , 2004, Journal of Neuro-Oncology.

[48]  Z L Gokaslan,et al.  A multivariate analysis of 416 patients with glioblastoma multiforme: prognosis, extent of resection, and survival. , 2001, Journal of neurosurgery.

[49]  N. Leeds,et al.  Imaging patterns of multifocal gliomas. , 1993, European journal of radiology.