Blood-based biomarkers for malignant gliomas

被引:36
作者
Holdhoff, Matthias [1 ]
Yovino, Susannah G. [1 ,2 ]
Boadu, Osei [1 ]
Grossman, Stuart A. [1 ]
机构
[1] Johns Hopkins Univ, Brain Canc Program, Dept Oncol, Sidney Kimmel Comprehens Canc Ctr,Sch Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Radiat Oncol & Mol Radiat Sci, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21287 USA
关键词
Malignant glioma; Glioblastoma; Circulating tumor DNA; Circulating tumor cells; Circulating biomarker; Blood-based biomarker; Pseudo-progression; HIGH-GRADE GLIOMAS; PHASE-II TRIAL; GLIOBLASTOMA-MULTIFORME; PROGNOSTIC VALUE; SERUM-LEVELS; PLASMA; DNA; THALIDOMIDE; GROWTH; MATRIX-METALLOPROTEINASE-9;
D O I
10.1007/s11060-013-1144-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant gliomas remain incurable and present unique challenges to clinicians, radiologists and clinical and translational investigators. One of the major problems in treatment of these tumors is our limited ability to reliably assess tumor response or progression. The most frequently used neuro-imaging studies (contrast-enhanced MRI and CT) rely on changes of blood-brain barrier (BBB) integrity, providing only an indirect assessment of tumor burden. In addition, the BBB can be altered by commonly used interventions including radiation, glucocorticoids and vascular endothelial growth factor inhibitors, further complicating the interpretation of scans. Newer radiologic techniques including PET and magnetic resonance spectroscopy are theoretically promising but thus far have not meaningfully changed the assessment of patients with malignant gliomas. A tumor-specific, blood-based biomarker would be of immediate use to clinicians and investigators if sufficiently sensitive and specific. This review discusses the potential utility of such a biomarker, the general classes of tumor-derived blood-based biomarkers and it summarizes the currently available data on circulating tumor cells, circulating nucleic acids and circulating proteins in patients with malignant gliomas. It is unclear which marker or marker class appears to be the most promising for these tumors. This article provides thoughts on how novel candidate blood-based markers could be discovered and tested in a more comprehensive way and why these efforts should be among the top priorities in neuro-oncologic research in the coming years.
引用
收藏
页码:345 / 352
页数:8
相关论文
共 44 条
[11]   Detection of IDH1 mutation in the plasma of patients with glioma [J].
Boisselier, Blandine ;
Perez-Larraya, Jaime Gallego ;
Rossetto, Marta ;
Labussiere, Marianne ;
Ciccarino, Pietro ;
Marie, Yannick ;
Delattre, Jean-Yves ;
Sanson, Marc .
NEUROLOGY, 2012, 79 (16) :1693-1698
[12]   Clinical features, mechanisms, and management of pseudoprogression in malignant gliomas [J].
Brandsma, Dieto ;
Stalpers, Lukas ;
Taal, Walter ;
Sminia, Peter ;
van den Bent, Martinj .
LANCET ONCOLOGY, 2008, 9 (05) :453-461
[13]   Serum levels of glial fibrillary acidic protein correlate to tumour volume of high-grade gliomas [J].
Brommeland, T. ;
Rosengren, L. ;
Fridlund, S. ;
Hennig, R. ;
Isaksen, V. .
ACTA NEUROLOGICA SCANDINAVICA, 2007, 116 (06) :380-384
[14]  
BURGER PC, 1983, APPL NEUROPHYSIOL, V46, P180
[15]   Myeloid Biomarkers Associated with Glioblastoma Response to Anti-VEGF Therapy with Aflibercept [J].
de Groot, John F. ;
Piao, Yuji ;
Hai Tran ;
Gilbert, Mark ;
Wu, Hua-Kang ;
Liu, Jun ;
Bekele, B. Nebiyou ;
Cloughesy, Tim ;
Mehta, Minesh ;
Robins, H. Ian ;
Lassman, Andrew ;
DeAngelis, Lisa ;
Camphausen, Kevin ;
Chen, Alice ;
Yung, W. K. A. ;
Prados, Michael ;
Wen, Patrick Y. ;
Heymach, John V. .
CLINICAL CANCER RESEARCH, 2011, 17 (14) :4872-4881
[16]   Circulating mutant DNA to assess tumor dynamics [J].
Diehl, Frank ;
Schmidt, Kerstin ;
Choti, Michael A. ;
Romans, Katharine ;
Goodman, Steven ;
Li, Meng ;
Thornton, Katherine ;
Agrawal, Nishant ;
Sokoll, Lori ;
Szabo, Steve A. ;
Kinzler, Kenneth W. ;
Vogelstein, Bert ;
Diaz, Luis A., Jr. .
NATURE MEDICINE, 2008, 14 (09) :985-990
[17]   BEAMing: single-molecule PCR on microparticles in water-in-oil emulsions [J].
Diehl, Frank ;
Li, Meng ;
He, Yiping ;
Kinzler, Kenneth W. ;
Vogelstein, Bert ;
Dressman, Devin .
NATURE METHODS, 2006, 3 (07) :551-559
[18]   Phase II trial of the antiangiogenic agent thalidomide in patients with recurrent high-grade gliomas [J].
Fine, HA ;
Figg, WD ;
Jaeckle, K ;
Wen, PY ;
Kyritsis, AP ;
Loeffler, JS ;
Levin, VA ;
Black, PM ;
Kaplan, R ;
Pluda, JM ;
Yung, WKA .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (04) :708-715
[19]   A North American brain tumor consortium (NABTC 99-04) phase II trial of temozolomide plus thalidomide for recurrent glioblastoma multiforme [J].
Groves, Morris D. ;
Puduvalli, Vinay K. ;
Chang, Susan M. ;
Conrad, Charles A. ;
Gilbert, Mark R. ;
Tremont-Lukats, Ivo W. ;
Liu, Ta-Jen ;
Peterson, Pamela ;
Schiff, David ;
Cloughesy, Timothy F. ;
Wen, Patrick Y. ;
Greenberg, Harry ;
Abrey, Lauren E. ;
DeAngelis, Lisa M. ;
Hess, Kenneth R. ;
Lamborn, Kathleen R. ;
Prados, Michael D. ;
Yung, W. K. Alfred .
JOURNAL OF NEURO-ONCOLOGY, 2007, 81 (03) :271-277
[20]   Transmission of tumours by transplantation [J].
Healey, PJ ;
Davis, CL .
LANCET, 1998, 352 (9121) :2-3