Egyszerű nézet

dc.contributor.author Kafatos G
dc.contributor.author Niepel D
dc.contributor.author Lowe K
dc.contributor.author Jenkins-Anderson S
dc.contributor.author Westhead H
dc.contributor.author Tímár, József
dc.contributor.author Tóth, Erika
dc.date.accessioned 2019-06-20T06:22:36Z
dc.date.available 2019-06-20T06:22:36Z
dc.date.issued 2017
dc.identifier.citation pagination=751-760; journalVolume=11; journalIssueNumber=9; journalTitle=BIOMARKERS IN MEDICINE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5129
dc.identifier.uri doi:10.2217/bmm-2016-0358
dc.description.abstract 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.
dc.relation.ispartof urn:issn:1752-0363
dc.title RAS mutation prevalence among patients with metastatic colorectal cancer: a meta-analysis of real-world data
dc.type Journal Article
dc.date.updated 2018-03-12T14:24:07Z
dc.language.rfc3066 en
dc.identifier.mtmt 3273953
dc.identifier.wos 000411390700008
dc.identifier.pubmed 28747067
dc.contributor.department SE/AOK/I/II. Sz. Patológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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