ForeSENTIA: Pan-Cancer Advanced

Synonyms: -
Material
Material:
FFPE tissue sections
Untersuchungsdauer
TAT:
2-3 weeks
Contact
Methode
Method:
NGS
Overview

The ForeSENTIA Pan-Cancer Advanced panel analyses single nucleotide variants, insertions, deletions, copy number alterations, and rearrangements in 392 genes associated with different types of cancers. It can help identify mutations that can be responsible for cancer development and therapy resistance in solid tumours. The clinical significance of the genes tested has been previously emphasised by professional bodies including , , and . Depending on the type of cancer and the genetic alterations identified, different /-approved drugs as well as eligible clinical trials are available.

Microsatellite instability (MSI) immunotherapy biomarker is also tested in this panel. /-approved immunotherapies are also available such as pembrolizumab for patients with MSI-high status depending on their type of cancer.

This panel also tests for Tumour Mutational Burden (TMB). TMB score can have a prognostic value for patients with any type of solid tumour. Studies have suggested that patients with TMB-H tumors should be considered for immunotherapy regardless of the tumours’ origin. For example, it was previously shown that TMB-H in ovarian cancer and cutaneous melanoma patients has an important role in prognosis. TMB-H status was also found to be associated with improved survival in different types of cancer – including NSCLC, head and neck cancer, melanoma, colorectal and other cancers – when treated with immunotherapy inhibitors. TMB is considered a new emerging tumour-agnostic biomarker. The -approved immunotherapy drug pembrolizumab can be used to treat all solid tumours with TMB-H, regardless of origin.

ForeSENTIA: Pan-Cancer Advanced
392 Gene(s)*
ABL1
ABL2
AKT1
AKT2
AKT3
ALK
ANKRD26
APC
AR
ARAF
ARID1A
ARID1B
ARID2
ARID5B
ASXL1
ATM
ATR
ATRIP
ATRX
AURKA
AURKB
AXIN2
B2M
BAP1
BARD1
BCL10
BCL2
BCL2L1
BCL2L11
BCL2L2
BCL6
BCOR
BCORL1
BCR
BLM
BMPR1A
BRAF
BRCA1
BRCA2
BRD4
BRINP1
BRIP1
BUB1B
CALR
CASP8
CBFB
CBL
CBLB
CBLC
CCAR2
CCND1
CCND2
CCND3
CCNE1
CD22
CD274
CD276
CD70
CD74
CD79A
CD79B
CDC25C
CDC73
CDH1
CDK12
CDK4
CDK6
CDK8
CDKN1A
CDKN1B
CDKN2A
CDKN2B
CDKN2C
CEBPA
CGAS
CHD2
CHD4
CHEK1
CHEK2
CIC
CREBBP
CSF1R
CSF3R
CTLA4
CTNNB1
CUX1
CXCR4
DCK
DDR2
DDX3X
DDX41
DEK
DHX15
DICER1
DNMT1
DNMT3A
DNMT3B
DPYD
DUSP22
E2F3
EGFR
EIF1AX
EP300
EPCAM
ERBB2
ERBB3
ERBB4
ERCC1
ERCC2
ERCC3
ERCC4
ERCC5
ERG
ESR1
ETNK1
ETV1
ETV4
ETV6
EWSR1
EZH1
EZH2
FANCA
FANCC
FANCD2
FANCE
FANCF
FANCG
FANCI
FANCL
FAS
FAT1
FBXW7
FGF1
FGF10
FGF12
FGF13
FGF14
FGF19
FGF2
FGF23
FGF3
FGF4
FGF5
FGF6
FGF7
FGF8
FGF9
FGFR1
FGFR2
FGFR3
FGFR4
FH
FLCN
FLT1
FLT3
FLT4
FOXA1
FOXL2
FOXO1
FRS2
FUBP1
GATA1
GATA2
GATA3
GATA4
GATA6
GEN1
GNA11
GNAQ
GNAS
GPC3
GREM1
GSK3B
H3F3A
HDAC1
HDAC2
HIST1H3B
HIST1H3C
HOXB13
HRAS
ID3
IDH1
IDH2
IFNGR1
IGF1
IGF1R
IGF2
IKZF1
IL10
IL3
IL7R
INHA
INSRR
IRF2
IRF4
IRS1
IRS2
JAK1
JAK2
JAK3
JUN
KAT6A
KDM5A
KDM5C
KDM6A
KDR
KEAP1
KIF5B
KIT
KLF5
KMT2A
KMT2B
KMT2C
KMT2D
KRAS
LATS1
LATS2
LTK
LUC7L2
MALT1
MAP2K1
MAP2K2
MAP2K4
MAP3K1
MAP3K13
MAP3K14
MAP3K4
MAPK1
MAPK3
MCL1
MDC1
MDM2
MDM4
MECOM
MED12
MEN1
MET
MGMT
MITF
MLH1
MLH3
MLLT3
MPL
MRE11
MSH2
MSH3
MSH6
MTAP
MTHFR
MTOR
MUTYH
MYC
MYCN
MYD88
MYH11
MYOD1
NBN
NCOA3
NCOR1
NCOR2
NF1
NF2
NFE2L2
NFKBIA
NOTCH1
NPM1
NRAS
NRG1
NTHL1
NTRK1
NTRK2
NTRK3
NUP214
NUTM1
PALB2
PARP1
PARP2
PARP3
PAX8
PBX1
PDCD1
PDCD1LG2
PDGFRA
PDGFRB
PGR
PHF6
PIK3CA
PIK3CB
PIK3CD
PIK3R1
PML
PMS2
POLD1
POLE
POLQ
PPM1D
PPP2R1A
PRKN
PRMT5
PSMB1
PSMB5
PTCH1
PTEN
PTPN11
RAC1
RAD21
RAD50
RAD51
RAD51B
RAD51C
RAD51D
RAD52
RAD54L
RAF1
RARA
RB1
RBBP6
RBM10
RECQL4
REL
RET
RHOA
RICTOR
RNF43
ROS1
RPS14
RUNX1
RUNX1T1
SDHA
SDHAF2
SDHB
SDHC
SDHD
SETBP1
SF3B1
SH2B3
SHOC2
SLC29A1
SMAD2
SMAD3
SMAD4
SMARCA4
SMARCB1
SMARCD1
SMC1A
SMC3
SMO
SOS1
SOX10
SPOP
SRC
SRSF2
STAG1
STAG2
STAT3
STAT4
STAT5A
STAT5B
STK11
SUFU
SUZ12
TCF3
TCL1A
TERT
TET2
TFRC
TGFBR1
TGFBR2
TMEM127
TMEM173
TMPRSS2
TOP1
TOP2A
TP53
TP63
TRAF2
TRAF7
TSC1
TSC2
TYMS
U2AF1
VEGFA
VHL
WRN
WT1
XPA
XPC
XPO1
XRCC2
YAP1
ZNF217
ZRSR2


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Our editorial team consists of medical specialists and scientists in the field of human genetics. All content is created and reviewed in accordance with current scientific standards.

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