Variation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trial

J Clin Pathol. 2015 Feb;68(2):111-8. doi: 10.1136/jclinpath-2014-202644. Epub 2014 Nov 27.

Abstract

Aims: Mutation detection accuracy has been described extensively; however, it is surprising that pre-PCR processing of formalin-fixed paraffin-embedded (FFPE) samples has not been systematically assessed in clinical context. We designed a RING trial to (i) investigate pre-PCR variability, (ii) correlate pre-PCR variation with EGFR/BRAF mutation testing accuracy and (iii) investigate causes for observed variation.

Methods: 13 molecular pathology laboratories were recruited. 104 blinded FFPE curls including engineered FFPE curls, cell-negative FFPE curls and control FFPE tissue samples were distributed to participants for pre-PCR processing and mutation detection. Follow-up analysis was performed to assess sample purity, DNA integrity and DNA quantitation.

Results: Rate of mutation detection failure was 11.9%. Of these failures, 80% were attributed to pre-PCR error. Significant differences in DNA yields across all samples were seen using analysis of variance (p<0.0001), and yield variation from engineered samples was not significant (p=0.3782). Two laboratories failed DNA extraction from samples that may be attributed to operator error. DNA extraction protocols themselves were not found to contribute significant variation. 10/13 labs reported yields averaging 235.8 ng (95% CI 90.7 to 380.9) from cell-negative samples, which was attributed to issues with spectrophotometry. DNA measurements using Qubit Fluorometry demonstrated a median fivefold overestimation of DNA quantity by Nanodrop Spectrophotometry. DNA integrity and PCR inhibition were factors not found to contribute significant variation.

Conclusions: In this study, we provide evidence demonstrating that variation in pre-PCR steps is prevalent and may detrimentally affect the patient's ability to receive critical therapy. We provide recommendations for preanalytical workflow optimisation that may reduce errors in down-stream sequencing and for next-generation sequencing library generation.

Keywords: LUNG CANCER; MELANOMA; MOLECULAR PATHOLOGY; PCR; diagnostic screening.

Publication types

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

MeSH terms

  • Cell Line, Tumor
  • DNA Mutational Analysis / methods
  • DNA Mutational Analysis / standards*
  • DNA, Neoplasm / genetics
  • DNA, Neoplasm / isolation & purification
  • Diagnostic Errors / prevention & control
  • ErbB Receptors / genetics*
  • Fixatives / standards*
  • Fluorometry / standards
  • Formaldehyde / standards*
  • Humans
  • Laboratory Proficiency Testing*
  • Mutation*
  • Observer Variation
  • Paraffin Embedding / standards*
  • Polymerase Chain Reaction / standards*
  • Predictive Value of Tests
  • Proto-Oncogene Proteins B-raf / genetics*
  • Reproducibility of Results
  • Spectrophotometry / standards
  • Tissue Fixation / methods
  • Tissue Fixation / standards*
  • Transfection
  • United Kingdom
  • United States
  • Workflow

Substances

  • DNA, Neoplasm
  • Fixatives
  • Formaldehyde
  • EGFR protein, human
  • ErbB Receptors
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf