biomarkers associated to treatment response and prognosis in

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26% 24% 50% Q3 Q2 Q1 Articles distribution in Quartile in Category Biomarkers associated to treatment response and prognosis in Glioblastoma Multiforme J. Pérez-Morales 1 , R. López-Sepúlveda 1 , M. Cañadas-Garre 1 , F.J. Orantes-Casado de Amezua 1 , A. Madrid-Paredes 1 , M.A. Calleja-Hernández 1 . 1 Hospital Universitario Virgen de las Nieves, Pharmacy, Granada, Spain. BACKGROUND: Gliomas represents more of 80% of malignant tumors of central nervous system. Glioblastoma Multiforme is the most aggressive glioma with an overage overall survival (OS) of 12 months, and the most prevalent, about 60-70% of all gliomas.chromosomal, genetic and epigenetic mutations in GBM are under investigation to determinate their role in clinical practice. PURPOSE Determine the main biomarkers evaluated for possible clinical utility in GBM MATERIAL AND METHODS Bibliographic review focused on biomarkers associated to treatment response/prognosis in GBM published in 2009 or later in a third or upper quartile in its category. RESULTS 42 Articles reviewed The main biomarkers identified Mutations involving isocitrate dehydrogenase 1p/19q deletion status O-6-methylguanine- DNA methyltransferase (MGMT) promoter methylation status MGMT status is the most acknowledged, being considered as predictive factor to chemotherapy response. MGMT gene encodes an enzyme that repairs the damage induced by O(6)-alkylating agents, as temozolomide. About 50% of patients show this promoter methylated in tumoral cells, resulting in low expression of this enzyme. Several studies show higher OS and free survival progression (FSP) in patients with methylated promoter. The most accepted method to determine promoter status is polymerase chain reaction after extraction of DNA and sodium bisulphite conversion. CONCLUSION MGMT promoter methylation status could help therapeutic managing of GBM patients. Although the role of this biomarker in GBM response to temozolomide is well known, it is not yet implemented in clinical routine for decision making CP-116

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Page 1: Biomarkers associated to treatment response and prognosis in

26%

24%

50% Q3

Q2

Q1

Articles distribution in Quartile in Category

Biomarkers associated to treatment response and prognosis in Glioblastoma Multiforme

J. Pérez-Morales1, R. López-Sepúlveda1, M. Cañadas-Garre1, F.J. Orantes-Casado de

Amezua1, A. Madrid-Paredes1, M.A. Calleja-Hernández1. 1Hospital Universitario Virgen de las Nieves, Pharmacy, Granada, Spain.

BACKGROUND:

Gliomas represents more of 80% of malignant tumors of central nervous system. Glioblastoma Multiforme is

the most aggressive glioma with an overage overall survival (OS) of 12 months, and the most prevalent,

about 60-70% of all gliomas.chromosomal, genetic and epigenetic mutations in GBM are under investigation

to determinate their role in clinical practice.

PURPOSE

Determine the main biomarkers evaluated for possible clinical utility in GBM

MATERIAL AND METHODS Bibliographic review focused on biomarkers associated to treatment response/prognosis in GBM published in 2009 or later in a third or upper quartile in its category.

RESULTS

42 Articles reviewed

The main biomarkers identified

Mutations involving isocitrate

dehydrogenase

1p/19q deletion status

O-6-methylguanine-DNA

methyltransferase (MGMT) promoter methylation status

MGMT status is the most acknowledged, being considered as predictive factor to chemotherapy response.

MGMT gene encodes an enzyme that repairs the damage induced by O(6)-alkylating agents, as temozolomide.

About 50% of patients show this promoter methylated in tumoral cells, resulting in low expression of this enzyme.

Several studies show higher OS and free survival progression (FSP) in patients with methylated promoter.

The most accepted method to determine promoter status is polymerase chain reaction after extraction of DNA and sodium bisulphite conversion.

CONCLUSION

MGMT promoter methylation status could help therapeutic managing of GBM patients. Although the role of this biomarker in GBM response to temozolomide is well known, it is not yet implemented in clinical routine for decision making

CP-116