Skip to main content
Dryad

Gene alterations, clinical informations and survival data of gliomas with/without corpus callosum involvement

Data files

Jun 24, 2021 version files 116.98 KB

Abstract

The raw dataset of this study contained the gene alterations, clinical informations and survival data of glioma patients. Gene alterations data were obtained by Next-generation DNA sequencing of glioma samples of patients. Clinical informations were obtained from Electronic medical records and follow-up. The survival data were obtained by follow-up of patients. In order to explore gene alterations and their correlation with the survival of glioblastoma (GBM) of corpus callosum (CC) involvement (ccGBM), this dataset was analyzed in detail. A total of 30 ccGBM and 88 non-ccGBM were finally included. The ccGBM had higher incidence of PDGFRA (33.3% versus 9.1%, P=0.004) alterations than non-ccGBM. PDGFRA amplification (PDGFRAamp, 33.3% versus 9.1%, P=0.004) and missense mutation (PDGFRAmut, 20.0% versus 3.4%, P=0.011) both had higher incidence in ccGBM than in non-ccGBM. PDGFRA alteration was significantly associated with the occurrence of ccGBM (OR=4.91 [95%CI: 1.55-15.52], P=0.007). The ccGBM of PDGFRAamp achieved shorter median PFS (8.6 versus 13.5 months, P=0.025) and OS (12.4 versus 17.9 months, P=0.022) than non-ccGBM of PDGFRAnon-amp. The ccGBM of PDGFRAamp combined with PDGFRAmut (PDGFRAamp-mut) had shorter median PFS (7.6 versus 8.9 months, P=0.022) and OS (9.6 versus 17.8 months, P=0.006) than non-ccGBM of PDGFRA wild type and non-amplification (PDGFRA-w, non-amp). Compared to ccGBM of PDGFRA-w, non-amp, the ccGBM of PDGFRAamp and PDGFRAamp-mut both had shorter median PFS and OS (P<0.05). Hazard ratios (HRs) of PDGFRAamp for PFS and OS of ccGBM were 3.08 (95%CI: 1.02-9.35, P=0.047) and 5.07 (95%CI: 1.52-16.89, P=0.008) respectively, HRs of PDGFRAamp-mut for PFS and OS were 13.16 (95%CI: 3.19-54.40, P<0.001) and 16.36 (95%CI: 2.66-100.70, P=0.003) respectively. The PDGFRA alterations is significantly associated with the occurrence and poor prognosis of ccGBM.