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Pediatric Disease Annotations & Medicines



   gliosarcoma
  

Disease ID 697
Disease gliosarcoma
Definition
Rare mixed tumors of the brain and rarely the spinal cord which contain malignant neuroectodermal (glial) and mesenchymal components, including spindle-shaped fibrosarcoma cells. These tumors are highly aggressive and present primarily in adults as rapidly expanding mass lesions. They may arise in tissue that has been previously irradiated. (From Br J Neurosurg 1995 Apr;9(2):171-8)
Synonym
[m]gliosarcoma
glioblastoma with a sarcomatous component
glioblastoma with sarcomatous component
glioblastoma with sarcomatous component (disorder)
glioma, sarcomatous
gliomas, sarcomatous
gliosarcoma (morphologic abnormality)
gliosarcoma [disease/finding]
gliosarcomas
sarcomatous glioma
sarcomatous gliomas
Orphanet
DOID
UMLS
C0206726
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:4)
C0035412  |  rhabdomyosarcoma  |  1
C0028945  |  oligodendroglioma  |  1
C1261473  |  sarcomas  |  1
C0206655  |  alveolar rhabdomyosarcoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:15)
TP53  |  7157  |  ORPHANET
FGFR1  |  2260  |  ORPHANET
IDH1  |  3417  |  ORPHANET
VEGFA  |  7422  |  CTD_human
POR  |  5447  |  CTD_human
FGFR3  |  2261  |  ORPHANET
PPARG  |  5468  |  ORPHANET
EGFR  |  1956  |  ORPHANET
CYP2B6  |  1555  |  CTD_human
LZTR1  |  8216  |  ORPHANET
MGMT  |  4255  |  ORPHANET
TACC3  |  10460  |  ORPHANET
NFKBIA  |  4792  |  ORPHANET
TACC1  |  6867  |  ORPHANET
CYP2C18  |  1562  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:106)
6591  |  SNAI2  |  DISEASES
123876  |  ACSM2A  |  DISEASES
5296  |  PIK3R2  |  DISEASES
51200  |  CPA4  |  DISEASES
3558  |  IL2  |  DISEASES
4940  |  OAS3  |  DISEASES
3820  |  KLRB1  |  DISEASES
3565  |  IL4  |  DISEASES
1958  |  EGR1  |  DISEASES
3998  |  LMAN1  |  DISEASES
2670  |  GFAP  |  DISEASES
2521  |  FUS  |  DISEASES
1022  |  CDK7  |  DISEASES
5156  |  PDGFRA  |  DISEASES
1019  |  CDK4  |  DISEASES
23205  |  ACSBG1  |  DISEASES
7057  |  THBS1  |  DISEASES
9360  |  PPIG  |  DISEASES
3417  |  IDH1  |  DISEASES
2581  |  GALC  |  DISEASES
6855  |  SYP  |  DISEASES
3827  |  KNG1  |  DISEASES
5924  |  RASGRF2  |  DISEASES
29999  |  FSCN3  |  DISEASES
5925  |  RB1  |  DISEASES
7157  |  TP53  |  DISEASES
55435  |  AP1AR  |  DISEASES
1956  |  EGFR  |  DISEASES
1030  |  CDKN2B  |  DISEASES
23082  |  PPRC1  |  DISEASES
341640  |  FREM2  |  DISEASES
2697  |  GJA1  |  DISEASES
1562  |  CYP2C18  |  DISEASES
3242  |  HPD  |  DISEASES
886  |  CCKAR  |  DISEASES
25976  |  TIPARP  |  DISEASES
308  |  ANXA5  |  DISEASES
1437  |  CSF2  |  DISEASES
3636  |  INPPL1  |  DISEASES
2587  |  GALR1  |  DISEASES
89927  |  C16orf45  |  DISEASES
11318  |  GPR182  |  DISEASES
4255  |  MGMT  |  DISEASES
23179  |  RGL1  |  DISEASES
1448  |  CSN3  |  DISEASES
646  |  BNC1  |  DISEASES
947  |  CD34  |  DISEASES
80153  |  EDC3  |  DISEASES
1351  |  COX8A  |  DISEASES
6657  |  SOX2  |  DISEASES
1555  |  CYP2B6  |  DISEASES
3326  |  HSP90AB1  |  DISEASES
2187  |  FANCB  |  DISEASES
8905  |  AP1S2  |  DISEASES
8811  |  GALR2  |  DISEASES
8519  |  IFITM1  |  DISEASES
63827  |  BCAN  |  DISEASES
3418  |  IDH2  |  DISEASES
23545  |  ATP6V0A2  |  DISEASES
4600  |  MX2  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
887  |  CCKBR  |  DISEASES
200162  |  SPAG17  |  DISEASES
1576  |  CYP3A4  |  DISEASES
3091  |  HIF1A  |  DISEASES
23583  |  SMUG1  |  DISEASES
2537  |  IFI6  |  DISEASES
309  |  ANXA6  |  DISEASES
80781  |  COL18A1  |  DISEASES
4763  |  NF1  |  DISEASES
56474  |  CTPS2  |  DISEASES
2157  |  F8  |  DISEASES
779  |  CACNA1S  |  DISEASES
1870  |  E2F2  |  DISEASES
5287  |  PIK3C2B  |  DISEASES
10763  |  NES  |  DISEASES
8771  |  TNFRSF6B  |  DISEASES
8945  |  BTRC  |  DISEASES
2334  |  AFF2  |  DISEASES
1580  |  CYP4B1  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
1503  |  CTPS1  |  DISEASES
1678  |  TIMM8A  |  DISEASES
896  |  CCND3  |  DISEASES
139596  |  UPRT  |  DISEASES
1896  |  EDA  |  DISEASES
2550  |  GABBR1  |  DISEASES
80036  |  TRPM3  |  DISEASES
168400  |  DDX53  |  DISEASES
9636  |  ISG15  |  DISEASES
10186  |  LHFP  |  DISEASES
161003  |  STOML3  |  DISEASES
7187  |  TRAF3  |  DISEASES
3161  |  HMMR  |  DISEASES
4938  |  OAS1  |  DISEASES
1029  |  CDKN2A  |  DISEASES
5270  |  SERPINE2  |  DISEASES
4193  |  MDM2  |  DISEASES
85476  |  GFM1  |  DISEASES
5447  |  POR  |  DISEASES
10480  |  EIF3M  |  DISEASES
6510  |  SLC1A5  |  DISEASES
2108  |  ETFA  |  DISEASES
4782  |  NFIC  |  DISEASES
440900  |  LINC01191  |  DISEASES
Locus
Symbol | Locus(Total Locus:12)
NFKBIA  |  14q13.2
SEPT14  |  7p11.2
LZTR1  |  22q11.21
EGFR  |  7p11.2
TP53  |  17p13.1
FGFR3  |  4p16.3
PPARG  |  3p25.2
TACC1  |  8p11.22
MGMT  |  10q26.3
TACC3  |  4p16.3
FGFR1  |  8p11.23
IDH1  |  2q34
Disease ID 697
Disease gliosarcoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:5)
HP:0001510  |  Growth deficiency  |  1
HP:0002859  |  Rhabdomyosarcoma  |  1
HP:0004948  |  Twisted blood vessels  |  1
HP:0009733  |  Glioma  |  1
HP:0006779  |  Alveolar rhabdomyosarcoma  |  1
Disease ID 697
Disease gliosarcoma
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:3)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0206726carmustineD002330154-93-8gliosarcomaMESH:D018316therapeutic15133626
C0206726cyclophosphamideD00352050-18-0gliosarcomaMESH:D018316therapeutic11389073
C0206726temozolomideC04724685622-93-1gliosarcomaMESH:D018316therapeutic20173548
FDA approved drug and dosage information(Total Drugs:2)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D018316temodartemozolomide5MGCAPSULE;ORALPrescriptionABYesNo
MESH:D018316temodartemozolomide100MG/VIALPOWDER;INTRAVENOUSPrescriptionNoneYesYes
FDA labeling changes(Total Drugs:2)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D01831611/3/2003temodartemozolomideRecurrent CNS tumorsTemozolomide effectiveness in children has not been demonstrated New data from 2 open-label Phase 2 studies in pediatric patients 3-18 years of age. In one study there were 29 patients with recurrent brain stem glioma and 34 patients with recurrent high grade astrocyoma. In a second study there were 122 patients enrolled with various types of tumors; 113 CNS tumors and 9 non-CNS tumors. The temozolomide toxicity profile in children is similar to adultsLabelingB---Schering11/20/2002FALSE'
MESH:D01831611/3/2003temodartemozolomideRecurrent CNS tumorsTemozolomide effectiveness in children has not been demonstrated New data from 2 open-label Phase 2 studies in pediatric patients 3-18 years of age. In one study there were 29 patients with recurrent brain stem glioma and 34 patients with recurrent high grade astrocyoma. In a second study there were 122 patients enrolled with various types of tumors; 113 CNS tumors and 9 non-CNS tumors. The temozolomide toxicity profile in children is similar to adultsLabelingB---Schering11/20/2002FALSE'