Evaluation of the Anyplex BRAF V600E real-time detection assay using dual-priming oligonucleotide technology in fine-needle aspirates of thyroid nodules

Ann Lab Med. 2015 Nov;35(6):624-9. doi: 10.3343/alm.2015.35.6.624.

Abstract

Background: Several molecular assays have been developed to detect the BRAF V600E mutation in fine needle aspirates (FNAs) for the diagnosis of papillary thyroid cancer. Using a multiplex PCR technique, we evaluated the Anyplex BRAF V600E Real-time Detection (Anyplex) assay and compared its efficacy with that of the Seeplex BRAF V600E ACE Detection (Seeplex) method.

Methods: We tested 258 consecutive FNA specimens using the Seeplex and Anyplex assays. Any conflicting results between the two assays were confirmed by using mutant enrichment with 3'-modified oligonucleotide (MEMO) sequencing. The limits of detection (LODs) and reproducibility for each assay were evaluated with serially diluted DNA from a BRAF V600E-positive cell line.

Results: The BRAF V600E mutation was detected in 36.4% (94/258) FNA specimens by either the Seeplex or Anyplex assay. Results for the two assays showed 93.4% (241/258) agreement, with a kappa value of 0.861 (95% confidence interval, 0.798-0.923). Of the eight specimens that were BRAF V600E-positive by the Anyplex assay but not by the Seeplex assay, five were found to be BRAF V600E-positive by MEMO sequencing. The mutation detection rate of the Seeplex and Anyplex assays was 79.0% and 84.0%, respectively, in the FNA specimens diagnosed as malignant (n=81). The LOD as determined by probit analysis was 0.046% (95% confidence interval, 0.019-0.532%).

Conclusions: The Anyplex assay performed better than the Seeplex assay with respect to the detection of the BRAF V600E mutation.

Keywords: Anyplex; BRAF V600E; Evaluation; Fine-needle aspiration; Real-time PCR; Seeplex.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Asian People / genetics
  • Biopsy, Fine-Needle
  • DNA / chemistry
  • DNA / metabolism
  • DNA Mutational Analysis / methods*
  • DNA Primers / metabolism*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Multiplex Polymerase Chain Reaction
  • Oligonucleotides / metabolism
  • Polymorphism, Single Nucleotide
  • Proto-Oncogene Proteins B-raf / genetics*
  • Republic of Korea
  • Thyroid Nodule / metabolism*
  • Thyroid Nodule / pathology

Substances

  • DNA Primers
  • Oligonucleotides
  • DNA
  • Proto-Oncogene Proteins B-raf