TMIC-17. DISCOVERING DOMINANT TUMOR CHARACTERISTICS IN CYSTIC GLIOBLASTOMA

التفاصيل البيبلوغرافية
العنوان: TMIC-17. DISCOVERING DOMINANT TUMOR CHARACTERISTICS IN CYSTIC GLIOBLASTOMA
المؤلفون: Zhihua Chen, Yifeng Miao, Shun Yao, Denis O’Meally, David Frankhouser, Biao Tang, MingHui Li, Paul Frankel, Mari Shahmanyan, Yongming Qiu, Russell C Rockne
المصدر: Neuro-Oncology. 24:vii274-vii275
بيانات النشر: Oxford University Press (OUP), 2022.
سنة النشر: 2022
مصطلحات موضوعية: Cancer Research, Oncology, Neurology (clinical)
الوصف: BACKGROUND As a rare subtype of glioblastoma (GBM), the genetic features and outcomes in cystic GBM (cGBM) are largely unknown. This study aimed to evaluate the survival of cystic features, investigate genomic patterns and the immune microenvironment in patients with cGBM. METHODS Gd T1-weighted, T2-weighted, T2-Flair, DWI or ADC images were used to classify cGBM or noncystic GBM (non-cGBM). Clinical information from IvyGAP, EGA databases and Chinese cohort were used for survival analysis. Fresh cystic fluid and residual tumor tissue were collected to evaluate immunological components, pathological and genomic differences between cGBM and non-cGBM. Data from IvyGAP were included to determine difference of molecular feature among substructure. RESULTS 143 cases with cGBM and non-cGBM were screened to compare survival outcomes. Cystic features were to confer a survival benefit. It was an independent prognostic factor irrespective of IDH, MGMT and therapeutic regimen. cGBM patients have a hypomethylation state compared to non-cGBM. Active immune cells such as CD4+, CD8+ T cells were present in the cystic fluid and infiltrated into tumor. 10 cytokines/chemokines were only detected in cystic fluid, 8 cytokines/chemokines increased two-fold in cystic fluid than in peripheral blood serum (PBPs). Much differential methylated position (DMPs), differentially expressed genes (DEGs), Gene Set Enrichment Analysis (GSAE), Functional Epigenetic Modules (FEM) networks and molecular feature of substructural regions were different between cGBM and non-cGBM. CONCLUSION These results imply that cGBM could be a new subtype and has distinctive immune microenvironment which may have potential value correlating with prognosis.
تدمد: 1523-5866
1522-8517
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::fc664f8dbfeebdb43af1c210fb085ed2Test
https://doi.org/10.1093/neuonc/noac209.1061Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........fc664f8dbfeebdb43af1c210fb085ed2
قاعدة البيانات: OpenAIRE