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Circulating MACC1 transcripts in glioblastoma patients predict prognosis and treatment response

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Item Type:Article
Title:Circulating MACC1 transcripts in glioblastoma patients predict prognosis and treatment response
Creators Name:Hagemann, C. and Neuhaus, N. and Dahlmann, M. and Kessler, A.F. and Kobelt, D. and Herrmann, P. and Eyrich, M. and Freitag, B. and Linsenmann, T. and Monoranu, C.M. and Ernestus, R.I. and Löhr, M. and Stein, U.
Abstract:Glioblastoma multiforme is the most aggressive primary brain tumor of adults, but lacks reliable and liquid biomarkers. We evaluated circulating plasma transcripts of metastasis-associated in colon cancer-1 (MACC1), a prognostic biomarker for solid cancer entities, for prediction of clinical outcome and therapy response in glioblastomas. MACC1 transcripts were significantly higher in patients compared to controls. Low MACC1 levels clustered together with other prognostically favorable markers. It was associated with patients' prognosis in conjunction with the isocitrate dehydrogenase (IDH) mutation status: IDH1 R132H mutation and low MACC1 was most favorable (median overall survival (OS) not yet reached), IDH1 wildtype and high MACC1 was worst (median OS 8.1 months), while IDH1 wildtype and low MACC1 was intermediate (median OS 9.1 months). No patients displayed IDH1 R132H mutation and high MACC1. Patients with low MACC1 levels receiving standard therapy survived longer (median OS 22.6 months) than patients with high MACC1 levels (median OS 8.1 months). Patients not receiving the standard regimen showed the worst prognosis, independent of MACC1 levels (low: 6.8 months, high: 4.4 months). Addition of circulating MACC1 transcript levels to the existing prognostic workup may improve the accuracy of outcome prediction and help define more precise risk categories of glioblastoma patients.
Keywords:Metastasis-Associated in Colon Cancer 1 (MACC1), Glioblastoma Multiforme, Liquid Biopsy, Therapy Response, Prognostic Marker
Page Range:825
Date:13 June 2019
Official Publication:https://doi.org/10.3390/cancers11060825
PubMed:View item in PubMed

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