Diagnostic and Therapeutic Biomarkers in Glioblastoma: Current Status and Future Perspectives

被引:229
作者
Szopa, Wojciech [1 ]
Burley, Thomas A. [2 ]
Kramer-Marek, Gabriela [2 ]
Kaspera, Wojciech [1 ]
机构
[1] Med Univ Silesia, Reg Hosp, Dept Neurosurg, Sosnowiec, Poland
[2] Inst Canc Res, Div Radiotherapy & Imaging, London, England
关键词
GROWTH-FACTOR RECEPTOR; MGMT PROMOTER METHYLATION; INTEGRATED GENOMIC ANALYSIS; MULTICENTER PHASE-II; HIGH-GRADE GLIOMAS; DNA-REPAIR GENE; PROGNOSTIC-SIGNIFICANCE; MALIGNANT ASTROCYTOMAS; ADJUVANT TEMOZOLOMIDE; MOLECULAR BIOMARKERS;
D O I
10.1155/2017/8013575
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glioblastoma (GBM) is a primary neuroepithelial tumor of the central nervous system, characterized by an extremely aggressive clinical phenotype. Patients with GBM have a poor prognosis and only 3-5% of them survive for more than 5 years. The current GBM treatment standards include maximal resection followed by radiotherapy with concomitant and adjuvant therapies. Despite these aggressive therapeutic regimens, the majority of patients suffer recurrence due to molecular heterogeneity of GBM. Consequently, a number of potential diagnostic, prognostic, and predictive biomarkers have been investigated. Some of them, such as IDH mutations, 1p19q deletion, MGMT promoter methylation, and EGFRvIII amplification are frequently tested in routine clinical practice. With the development of sequencing technology, detailed characterization of GBM molecular signatures has facilitated a 6more personalized therapeutic approach and contributed to the development of a new generation of anti-GBM therapies such as molecular inhibitors targeting growth factor receptors, vaccines, antibody-based drug conjugates, and more recently inhibitors blocking the immune checkpoints. In this article, we review the exciting progress towards elucidating the potential of current and novel GBM biomarkers and discuss their implications for clinical practice.
引用
收藏
页数:13
相关论文
共 141 条
  • [1] Scatter factor/hepatocyte growth factor in brain tumor growth and angiogenesis
    Abounader, R
    Laterra, J
    [J]. NEURO-ONCOLOGY, 2005, 7 (04) : 436 - 451
  • [2] Overall Survival of Newly Diagnosed Glioblastoma Patients Receiving Carmustine Wafers Followed by Radiation and Concurrent Temozolomide Plus Rotational Multiagent Chemotherapy
    Affronti, Mary Lou
    Heery, Christopher R.
    Herndon, James E., II
    Rich, Jeremy N.
    Reardon, David A.
    Desjardins, Annick
    Vredenburgh, James J.
    Friedman, Allan H.
    Bigner, Darell D.
    Friedman, Henry S.
    [J]. CANCER, 2009, 115 (15) : 3501 - 3511
  • [3] Glioblastoma: pathology, molecular mechanisms and markers
    Aldape, Kenneth
    Zadeh, Gelareh
    Mansouri, Sheila
    Reifenberger, Guido
    von Deimling, Andreas
    [J]. ACTA NEUROPATHOLOGICA, 2015, 129 (06) : 829 - 848
  • [4] Glioblastoma multiforme: Pathogenesis and treatment
    Alifieris, Constantinos
    Trafalis, Dimitrios T.
    [J]. PHARMACOLOGY & THERAPEUTICS, 2015, 152 : 63 - 82
  • [5] [Anonymous], 2007, ACTA NEUROPATHOL, DOI DOI 10.1007/s00401-007-0243-4
  • [6] Molecular Pathways in Gliomagenesis and Their Relevance to Neuropathologic Diagnosis
    Appin, Christina L.
    Brat, Daniel J.
    [J]. ADVANCES IN ANATOMIC PATHOLOGY, 2015, 22 (01) : 50 - 58
  • [7] Net Clinical Benefit Analysis of Radiation Therapy Oncology Group 0525: A Phase III Trial Comparing Conventional Adjuvant Temozolomide With Dose-Intensive Temozolomide in Patients With Newly Diagnosed Glioblastoma
    Armstrong, Terri S.
    Wefel, Jeffrey S.
    Wang, Meihua
    Gilbert, Mark R.
    Won, Minhee
    Bottomley, Andrew
    Mendoza, Tito R.
    Coens, Corneel
    Werner-Wasik, Maria
    Brachman, David G.
    Choucair, Ali K.
    Mehta, Minesh
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (32) : 4076 - +
  • [8] Molecular and cellular heterogeneity: the hallmark of glioblastoma
    Aum, Diane J.
    Kim, David H.
    Beaumont, Thomas L.
    Leuthardt, Eric C.
    Dunn, Gavin P.
    Kim, Albert H.
    [J]. NEUROSURGICAL FOCUS, 2014, 37 (06)
  • [9] Percent Change of Perfusion Skewness and Kurtosis: A Potential Imaging Biomarker for Early Treatment Response in Patients with Newly Diagnosed Glioblastomas
    Baek, Hye Jin
    Kim, Ho Sung
    Kim, Namkug
    Choi, Young Jun
    Kim, Young Joong
    [J]. RADIOLOGY, 2012, 264 (03) : 834 - 843
  • [10] Differentiation of Recurrent Glioblastoma Multiforme from Radiation Necrosis after External Beam Radiation Therapy with Dynamic Susceptibility-weighted Contrast-enhanced Perfusion MR Imaging
    Barajas, Ramon F., Jr.
    Chang, Jamie S.
    Segal, Mark R.
    Parsa, Andrew T.
    McDermott, Michael W.
    Berger, Mitchel S.
    Cha, Soonmee
    [J]. RADIOLOGY, 2009, 253 (02) : 486 - 496