The role of liquid biopsy in the diagnosis of glioblastoma progression
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Published:2022-06-29
Issue:3
Volume:21
Page:104-116
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ISSN:2312-3168
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Container-title:Siberian journal of oncology
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language:
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Short-container-title:Sib. onkol. ž.
Author:
Ryabova A. I.1ORCID, Novikov V. A.2ORCID, Choynzonov E. L.2ORCID, Spirina L. V.2ORCID, Yunusova N. V.2ORCID, Ponomareva A. A.1ORCID, Tamkovich S. N.3, Gribova O. V.1ORCID
Affiliation:
1. Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences 2. Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences; Siberian State Medical University of the Ministry of Health of Russia 3. Siberian Branch of Russian Academy of Sciences; Department of Clinical Biochemistry, Novosibirsk State University
Abstract
Purpose: to summarize available data on the diagnostic value of various circulating biomarkers for the detection of glioblastoma recurrence. Material and Methods. A literature search was conducted using PubMED ExoCarta and SILVA databases. Results. Glioblastoma multiforme (GBM) is the most common glioma in adults with an unfavorable prognosis. Treatment of tumor recurrence can improve the survival of patients. Neuroimaging is the standard method of diagnosing brain tumor recurrence. However, a neuroimaging method to clearly distinguish between pseudo progression and tumor progression has not been found to date. Current molecular tumor profling relies heavily on tissue resection or biopsy. Tissue profling has several disadvantages in the central nervous system’s tumors, including the challenge associated with invasive biopsy, the heterogeneous nature of many malignancies where a small biopsy can under represent the mutational profle. Liquid biopsy is a promising method in diagnosing malignant tumors. Blood collection is a simple, minimally invasive procedure, but cerebrospinal fuid allows tumor markers to be detected more confdently. However, collection of cerebrospinal fuid is a complex and invasive procedure that can be accompanied by serious complications. Conclusion. Biological fuid markers such as circulating tumor cells, extracellular vesicles, cell-free DNA and cell-free RNA allow for the detection of GMB, determination of molecular genetic features of cancer during response to therapy, and early detection of GBM recurrence.
Publisher
Tomsk Cancer Research Institute
Subject
Cancer Research,Oncology
Reference115 articles.
1. Ostrom Q.T., Cioff G., Gittleman H., Patil N., Waite K., Kruchko C., Barnholtz-Sloan J.S. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2012– 2016. Neuro Oncol. 2019; 21(5):1–100. doi: 10.1093/neuonc/noz150. 2. Chinot O.L., Wick W., Mason W., Henriksson R., Saran F., Nishikawa R., Carpentier A.F., Hoang-Xuan K., Kavan P., Cernea D., Brandes A.A., Hilton M., Abrey L., Cloughesy T. Bevacizumab plus radiotherapytemozolomide for newly diagnosed glioblastoma. N Engl J Med. 2014; 370(8): 709–22. doi: 10.1056/NEJMoa1308345. 3. Gilbert M.R., Dignam J.J., Armstrong T.S., Wefel J.S., Blumenthal D.T., Vogelbaum M.A., Colman H., Chakravarti A., Pugh S., Won M., Jeraj R., Brown P.D., Jaeckle K.A., Schiff D., Stieber V.W., Brachman D.G., WernerWasik M., Tremont-Lukats I.W., Sulman E.P., Aldape K.D., Curran W.J. Jr., Mehta M.P. A randomized trial of bevacizumab for newly diagnosed glioblastoma. N Engl J Med. 2014; 370(8): 699–708. doi: 10.1056/ NEJMoa1308573. 4. Stupp R., Taillibert S., Kanner A., Read W., Steinberg D., Lhermitte B., Toms S., Idbaih A., Ahluwalia M.S., Fink K., Di Meco F., Lieberman F., Zhu J.J., Stragliotto G., Tran D., Brem S., Hottinger A., Kirson E.D., Lavy-Shahaf G., Weinberg U., Kim C.Y., Paek S.H., Nicholas G., Bruna J., Hirte H., Weller M., Palti Y., Hegi M.E., Ram Z. Efect of Tumor-Treating Fields Plus Maintenance Temozolomide vs Maintenance Temozolomide Alone on Survival in Patients With Glioblastoma: A Randomized Clinical Trial. JAMA. 2017; 318(23): 2306–16. doi: 10.1001/jama.2017.18718. 5. Louis D.N., Perry A., Reifenberger G., von Deimling A., FigarellaBranger D., Cavenee W.K., Ohgaki H., Wiestler O.D., Kleihues P., Ellison D.W. The 2016 World Health Organization Classifcation of Tumors of the Central Nervous System: a summary. Acta Neuropathol. 2016; 131(6): 803–20. doi: 10.1007/s00401-016-1545-1.
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