-
Je něco špatně v tomto záznamu ?
RAS mutation prevalence among patients with metastatic colorectal cancer: a meta-analysis of real-world data
G. Kafatos, D. Niepel, K. Lowe, S. Jenkins-Anderson, H. Westhead, T. Garawin, Z. Traugottová, A. Bilalis, E. Molnar, J. Timar, E. Toth, N. Gouvas, G. Papaxoinis, S. Murray, N. Mokhtar, H. Vosmikova, P. Fabian, A. Skalova, P. Wójcik, A....
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, metaanalýza, práce podpořená grantem
NLK
PubMed Central
od 2015 do Před 1 rokem
ProQuest Central
od 2007-06-01 do 2021-01-31
Health & Medicine (ProQuest)
od 2007-06-01 do 2021-01-31
Public Health Database (ProQuest)
od 2007-06-01 do 2021-01-31
PubMed
28747067
DOI
10.2217/bmm-2016-0358
Knihovny.cz E-zdroje
- MeSH
- exony MeSH
- kolorektální nádory epidemiologie mortalita patologie MeSH
- lidé MeSH
- míra přežití MeSH
- mutace MeSH
- nádorové biomarkery genetika MeSH
- prevalence MeSH
- protoonkogenní proteiny B-raf genetika MeSH
- protoonkogenní proteiny p21(ras) genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
- práce podpořená grantem MeSH
AIM: A confirmed wild-type RAS tumor status is commonly required for prescribing anti-EGFR treatment for metastatic colorectal cancer. This noninterventional, observational research project estimated RAS mutation prevalence from real-world sources. MATERIALS & METHODS: Aggregate RAS mutation data were collected from 12 sources in three regions. Each source was analyzed separately; pooled prevalence estimates were then derived from meta-analyses. RESULTS: The pooled RAS mutation prevalence from 4431 tumor samples tested for RAS mutation status was estimated to be 43.6% (95% CI: 38.8-48.5%); ranging from 33.7% (95% CI: 28.4-39.3%) to 54.1% (95% CI: 51.7-56.5%) between sources. CONCLUSION: The RAS mutation prevalence estimates varied among sources. The reasons for this are not clear and highlight the need for further research.
Adelphi Research Manchester UK
Amgen Hellas EPE Athens Greece
Amgen Inc Thousand Oaks CA USA
Amgen s r o Prague Czech Republic
Bioptická laboratoř Plzeň Czech Republic
Centrum Onkologii Instytut im Marii Sklodowskiej Curie Warsaw Poland
Gastrointestinal Cancer Study Group Heraklion Crete Greece
Hellenic Cooperative Oncology Group University of Athens Athens Greece
Masaryk Memorial Cancer Institute Brno Czech Republic
National Cancer Institute Cairo University Cairo Egypt
National Institute of Oncology Budapest Hungary
Oncogene Diagnostics Sp z o o Krakow Poland
Radboud University Medical Center Nijmegen The Netherlands
Semmelweis Medical University Budapest Hungary
University Hospital Frankfurt Germany
University Hospital Hradec Kralove Hradec Kralove Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19028771
- 003
- CZ-PrNML
- 005
- 20190819121331.0
- 007
- ta
- 008
- 190813s2017 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.2217/bmm-2016-0358 $2 doi
- 035 __
- $a (PubMed)28747067
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Kafatos, George $u Amgen Ltd, Uxbridge, UK.
- 245 10
- $a RAS mutation prevalence among patients with metastatic colorectal cancer: a meta-analysis of real-world data / $c G. Kafatos, D. Niepel, K. Lowe, S. Jenkins-Anderson, H. Westhead, T. Garawin, Z. Traugottová, A. Bilalis, E. Molnar, J. Timar, E. Toth, N. Gouvas, G. Papaxoinis, S. Murray, N. Mokhtar, H. Vosmikova, P. Fabian, A. Skalova, P. Wójcik, A. Tysarowski, M. Barugel, JH. van Krieken, J. Trojan,
- 520 9_
- $a AIM: A confirmed wild-type RAS tumor status is commonly required for prescribing anti-EGFR treatment for metastatic colorectal cancer. This noninterventional, observational research project estimated RAS mutation prevalence from real-world sources. MATERIALS & METHODS: Aggregate RAS mutation data were collected from 12 sources in three regions. Each source was analyzed separately; pooled prevalence estimates were then derived from meta-analyses. RESULTS: The pooled RAS mutation prevalence from 4431 tumor samples tested for RAS mutation status was estimated to be 43.6% (95% CI: 38.8-48.5%); ranging from 33.7% (95% CI: 28.4-39.3%) to 54.1% (95% CI: 51.7-56.5%) between sources. CONCLUSION: The RAS mutation prevalence estimates varied among sources. The reasons for this are not clear and highlight the need for further research.
- 650 _2
- $a nádorové biomarkery $x genetika $7 D014408
- 650 _2
- $a kolorektální nádory $x epidemiologie $x mortalita $x patologie $7 D015179
- 650 _2
- $a exony $7 D005091
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mutace $7 D009154
- 650 _2
- $a prevalence $7 D015995
- 650 _2
- $a protoonkogenní proteiny B-raf $x genetika $7 D048493
- 650 _2
- $a protoonkogenní proteiny p21(ras) $x genetika $7 D016283
- 650 _2
- $a míra přežití $7 D015996
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a metaanalýza $7 D017418
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Niepel, Daniela $u Amgen GmbH, Vienna, Austria.
- 700 1_
- $a Lowe, Kimberley $u Amgen Inc., Thousand Oaks, CA, USA.
- 700 1_
- $a Jenkins-Anderson, Sophie $u Adelphi Research (Global), Manchester, UK.
- 700 1_
- $a Westhead, Hal $u Adelphi Research (Global), Manchester, UK.
- 700 1_
- $a Garawin, Tamer $u Amgen Inc., Thousand Oaks, CA, USA.
- 700 1_
- $a Traugottová, Zuzana $u Amgen s.r.o., Prague, Czech Republic.
- 700 1_
- $a Bilalis, Antonios $u Amgen Hellas EPE, Athens, Greece.
- 700 1_
- $a Molnar, Edit $u Amgen Kft, Budapest, Hungary.
- 700 1_
- $a Timar, Jozsef $u Semmelweis Medical University, Budapest, Hungary.
- 700 1_
- $a Toth, Erika $u National Institute of Oncology, Budapest, Hungary.
- 700 1_
- $a Gouvas, Nikolaos $u Gastrointestinal Cancer Study Group, Heraklion, Crete, Greece.
- 700 1_
- $a Papaxoinis, George $u Hellenic Cooperative Oncology Group, University of Athens, Athens, Greece.
- 700 1_
- $a Murray, Samuel $u Biomarker Solutions, London, UK.
- 700 1_
- $a Mokhtar, Nadia $u National Cancer Institute, Cairo University, Cairo, Egypt.
- 700 1_
- $a Vosmikova, Hana $u University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
- 700 1_
- $a Fabian, Pavel $u Masaryk Memorial Cancer Institute, Brno, Czech Republic.
- 700 1_
- $a Skalova, Alena $u Bioptická laboratoř, Plzeň, Czech Republic.
- 700 1_
- $a Wójcik, Piotr $u Oncogene Diagnostics Sp.z.o.o., Krakow, Poland.
- 700 1_
- $a Tysarowski, Andrzej $u Centrum Onkologii Instytut im. Marii Sklodowskiej Curie, Warsaw, Poland.
- 700 1_
- $a Barugel, Mario $u Tecnofarma, Santiago, Chile.
- 700 1_
- $a van Krieken, J Han $u Radboud University Medical Center, Nijmegen, The Netherlands.
- 700 1_
- $a Trojan, Jörg $u University Hospital, Frankfurt, Germany.
- 773 0_
- $w MED00172897 $t Biomarkers in medicine $x 1752-0371 $g Roč. 11, č. 9 (2017), s. 751-760
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28747067 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190813 $b ABA008
- 991 __
- $a 20190819121605 $b ABA008
- 999 __
- $a ok $b bmc $g 1433920 $s 1067231
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 11 $c 9 $d 751-760 $e 20170727 $i 1752-0371 $m Biomarkers in medicine $n Biomark Med $x MED00172897
- LZP __
- $a Pubmed-20190813