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      Karnofsky Performance Scale and Neurological Assessment of Neuro-Oncology Scale as Early Predictor in Glioma

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          Abstract

          Objective:

          Glioma is one of the most frequent and disabling primary brain tumour. Patients are not only dealing with survival, but also quality of life, which remains another major concern. Karnofsky Performance Scale (KPS) is one of the most commonly used scale to assess patients’ quality of life. A recent scale, known as Neurological Assessment of Neuro-Oncology Scale, has surfaced to examine neurological disability caused by brain tumour. Previous study showed this scale to be superior to KPS in predicting survival. However, these scales have never been used to foresee functional scale improvement during disease progression. We sought to determine whether initial KPS and NANO Scale can predict functional scale improvement 2 months after surgery.

          Methods:

          Patients with glioma grade II-IV were included in the study. IDH mutation and MGMT methylation were tested. KPS and NANO scale were examined before surgery and 2 months after surgery. Favorable outcome (FO) was defined as improvement in functional scale 2 months after surgery. Patients initial functional scales were analyzed towards favorable outcome.

          Results:

          Glioma WHO grade II, III and IV was found in 17 patients (36.2%), 3 patients (6.4%) and 27 patients (57.4%) respectively. Median KPS before and 2 months after surgery were 50 (30-80) and 60 (0-100), whereas median NANO scale before and 2 months after surgery were 5 (0-12) and 3 (0-12). Favorable outcome was found in 63.8% (KPS) and 78.7% (NANO Scale). Patients initial functional scales were significantly related to FO.

          Conclusion:

          Good initial functional scales are 4 to 5 times likely of having a favorable outcome 2 months after surgery.

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          Most cited references19

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          IDH1 and IDH2 mutations in gliomas.

          A recent genomewide mutational analysis of glioblastomas (World Health Organization [WHO] grade IV glioma) revealed somatic mutations of the isocitrate dehydrogenase 1 gene (IDH1) in a fraction of such tumors, most frequently in tumors that were known to have evolved from lower-grade gliomas (secondary glioblastomas). We determined the sequence of the IDH1 gene and the related IDH2 gene in 445 central nervous system (CNS) tumors and 494 non-CNS tumors. The enzymatic activity of the proteins that were produced from normal and mutant IDH1 and IDH2 genes was determined in cultured glioma cells that were transfected with these genes. We identified mutations that affected amino acid 132 of IDH1 in more than 70% of WHO grade II and III astrocytomas and oligodendrogliomas and in glioblastomas that developed from these lower-grade lesions. Tumors without mutations in IDH1 often had mutations affecting the analogous amino acid (R172) of the IDH2 gene. Tumors with IDH1 or IDH2 mutations had distinctive genetic and clinical characteristics, and patients with such tumors had a better outcome than those with wild-type IDH genes. Each of four tested IDH1 and IDH2 mutations reduced the enzymatic activity of the encoded protein. Mutations of NADP(+)-dependent isocitrate dehydrogenases encoded by IDH1 and IDH2 occur in a majority of several types of malignant gliomas. 2009 Massachusetts Medical Society
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            CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2011–2015

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              • Article: not found

              CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2008-2012.

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                Author and article information

                Journal
                Asian Pac J Cancer Prev
                Asian Pac J Cancer Prev
                APJCP
                Asian Pacific Journal of Cancer Prevention : APJCP
                West Asia Organization for Cancer Prevention (Iran )
                1513-7368
                2476-762X
                November 2020
                : 21
                : 11
                : 2287-3392
                Affiliations
                [1 ] Department of Neurology, Faculty of Medicine, Universitas Pelita Harapan, Jl. M.H.Thamrin Boulevard 1100, Lippo Village, Tangerang 15811, Indonesia.
                [2 ] Department of Neurosurgery, Faculty of Medicine, Universitas Hasanuddin, Jl.Perintis Kemerdekaan KM 10, Makassar, Indonesia.
                [3 ] Department of Neurosurgery, Faculty of Medicine, Universitas Pelita Harapan, Jl. M.H.Thamrin Boulevard 1100, Lippo Village, Tangerang 15811, Indonesia.
                [4 ] Department of Physiology, Faculty of Medicine, Universitas Hasanuddin, Jl.Perintis Kemerdekaan KM 10, Makassar, Indonesia.
                [5 ] Molecular Biology and Immunology Laboratory, Faculty of Medicine, Universitas Hasanuddin, Jl.Perintis Kemerdekaan KM 10, Makassar, Indonesia.
                [6 ] 6 Department of Neurology, Faculty of Medicine, Universitas Indonesia. Jl. Diponegoro No.71, Jakarta, Indonesia.
                Author notes
                [* ]For Correspondence: pricilla.gunawan@uph.edu
                Article
                10.31557/APJCP.2020.21.11.3387
                8033113
                33247700
                1054cf43-07a9-4b23-8723-ecfabcd49b49

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License, ( http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 August 2020
                : 6 November 2020
                Categories
                Research Article

                functional scale,kps,nano scale,glioma
                functional scale, kps, nano scale, glioma

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