Evidence map›Paper›PMID 22022941›Full record

ArticleExpert review of molecular diagnostics2011

Detection of KRAS and BRAF mutations in advanced colorectal cancer by allele-specific single-base primer extension.

Katharina Balschun, Ann-Kathrin Wenke, Christoph Röcken, Jochen Haag

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Article in Expert review of molecular diagnostics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Katharina BalschunInstitute of Pathology, Christian-Albrechts-University, Arnold-Heller-Str. 3, D-24105 Kiel, Germany.
Ann-Kathrin Wenke
Christoph Röcken
Jochen Haag

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evaluation of: Magnin S, Viel E, Baraquin A et al. A multiplex SNaPshot assay as a rapid method for detecting KRAS and BRAF mutations in advanced colorectal cancers. J. Mol. Diagn. 13(5), 485-492 (2011). Since mutations in the KRAS and BRAF genes are associated with resistance to therapy with anticancer drugs targeting the EGF receptor pathway, the analysis of KRAS and BRAF mutational status has become an important tool in the clinical management of patients with advanced colorectal cancer. To be useful in the clinical setting, a diagnostic assay has to address several issues related to the sensitivity and specificity of the method, the modularity of the assay, the turnaround time and the running costs. A variety of methods have been applied to the diagnosis of KRAS and BRAF mutational status. Although there is a good concordance between different methods, differences exist regarding sensitivity, multiplexing capacity and costs. In this article, we review a recently published assay for the simultaneous detection of diagnostically relevant KRAS and BRAF mutations and discuss this work in the context of conventional diagnostic methods.

Identifiers

PMID22022941

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.