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Usage of tissue microRNAs for identification of patients who will benefit from the adjuvant radiotherapy after surgical resection of atypical meningioma

Project goals

Meningiomas comprise 13-30% of primary intracranial tumors. They are often asymptomatic and have slow growth. However, grade II and III meningiomas are more likely to develop invasive disease and present a higher recurrence rate after surgical treatment or adjuvant radiation therapy. Surgical resection is the mainstay treatment for symptomatic meningiomas and it is also option for young asymptomatic patients presenting accessible tumors, since there is a possibility of complete resection. Adjuvant RT is advocated in case of incomplete surgical resection and in the presence of grade II or III meningiomas, due to the greater risk of local recurrence. However, there are not biomarkers able to predict patients who develop early recurrence and who will benefit from adjuvant radiotherapy. MicroRNAs were described to be significantly deregulated in meningioma and to be involved in processes associated with radioresistance. From this perspective, analysis of microRNAs in meningioma presents a promising approach enabling more accurate prediction of risk of recurrence of meningioma patients.

Keywords

mikroRNAmicroRNAbiomarkerbiomarkerradioterapieradiotherapymeningeommeningioma

Public support

  • Provider

    Ministry of Health

  • Programme

    Programme to support medical applied research in 2015 to 2022

  • Call for proposals

    Zdravotnický AV 5 (SMZ0201900001)

  • Main participants

    Fakultní nemocnice Brno

  • Contest type

    VS - Public tender

  • Contract ID

    NV19-03-00559

Alternative language

  • Project name in Czech

    Využití tkáňových mikroRNA pro identifikaci pacientů majících benefit z adjuvantní radioterapie po chirurgickém odstranění atypického meningeomu

  • Annotation in Czech

    Meningeomy představují 13-30 % všech primárních intrakraniálních tumorů. Přesto, že jsou typické asymptomatickým průběhem a pomalým růstem, u meningeomů grade II a III dochází často k rozvoji invazivního onemocnění a významně vyššímu výskytu rekurence po chirurgické resekci nebo adjuvantní radioterapii. Chirurgická resekce představuje základní léčebnou modalitu u symptomatických meningeomů i mladých asymptomatických pacientů s přístupnými tumory z důvodu možnosti kompletní resekce. Adjuvantní radioterapie je indikována v případě neúplné chirurgické resekce tumoru a u meningeomů grade II a III kvůli většímu riziku lokální rekurence. V současnosti nejsou známy biomarkery schopné predikovat pacienty s časnou rekurencí a pacienty, kteří by těžili z adjuvantní terapie. Deregulace hladin mikroRNA byla pozorována jak v souvislosti s meningeomy, tak s radiorezistencí nádorových onemocnění. Analýza miRNA by z tohoto důvodu mohla sloužit jako slibný nástroj pro přesnější predikci rizika progrese meningeomu.

Scientific branches

  • R&D category

    AP - Applied research

  • OECD FORD - main branch

    30204 - Oncology

  • OECD FORD - secondary branch

  • OECD FORD - another secondary branch

  • FD - Oncology and haematology

Completed project evaluation

  • Provider evaluation

    U - Uspěl podle zadání (s publikovanými či patentovanými výsledky atd.)

  • Project results evaluation

    The project has met all the objectives set out in the approved proposal and the project has a practical impact on clinical medicine in the treatment of meningiomas. Specifically, miRNAs differential expression in atypical meningioma tissue is able to predict the occurrence of relapse within five years of surgical intervention in patients who have identically undergone adjuvant radiotherapy have been identified. At the same time, microRNAs associated with disease recurrence were identified in meningioma patients enrolled in the study regardless of their postoperative treatment. Beyond the planned outcomes, microRNAs with differential expression were identified in very stiff meningiomas compared with soft and well-surgically removable tumors. The achieved results were sequentially incorporated into 5 publications in open access journals with IF (3 manuscripts are under review), one article in proceedings and one book chapter.

Solution timeline

  • Realization period - beginning

    May 1, 2019

  • Realization period - end

    Dec 31, 2023

  • Project status

    U - Finished project

  • Latest support payment

    Apr 28, 2023

Data delivery to CEP

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

  • Data delivery code

    CEP24-MZ0-NV-U

  • Data delivery date

    Jul 3, 2024

Finance

  • Total approved costs

    8,319 thou. CZK

  • Public financial support

    8,289 thou. CZK

  • Other public sources

    0 thou. CZK

  • Non public and foreign sources

    30 thou. CZK