JCO Global Oncology (May 2023)

QPOLE: A Quick, Simple, and Cheap Alternative for POLE Sequencing in Endometrial Cancer by Multiplex Genotyping Quantitative Polymerase Chain Reaction

  • Anne Sophie V.M. Van den Heerik,
  • Natalja T. Ter Haar,
  • Lisa Vermij,
  • Jan J. Jobsen,
  • Mariel Brinkhuis,
  • Suzan M. Roothaan,
  • Alicia Leon-Castillo,
  • Gitte Ortoft,
  • Estrid Hogdall,
  • Claus Hogdall,
  • Tom Van Wezel,
  • Ludy C.H.W. Lutgens,
  • Marie A.D. Haverkort,
  • Jas Khattra,
  • Jessica N. McAlpine,
  • Carien L. Creutzberg,
  • Vincent T.H.B.M. Smit,
  • C. Blake Gilks,
  • Nanda Horeweg,
  • Tjalling Bosse

DOI
https://doi.org/10.1200/GO.22.00384
Journal volume & issue
no. 9

Abstract

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PURPOSEDetection of 11 pathogenic variants in the POLE gene in endometrial cancer (EC) is critically important to identify women with a good prognosis and reduce overtreatment. Currently, POLE status is determined by DNA sequencing, which can be expensive, relatively time-consuming, and unavailable in hospitals without specialized equipment and personnel. This may hamper the implementation of POLE-testing in clinical practice. To overcome this, we developed and validated a rapid, low-cost POLE hotspot test by a quantitative polymerase chain reaction (qPCR) assay, QPOLE.MATERIALS AND METHODSPrimer and fluorescence-labeled 5′-nuclease probe sequences of the 11 established pathogenic POLE mutations were designed. Three assays, QPOLE-frequent for the most common mutations and QPOLE-rare-1 and QPOLE-rare-2 for the rare variants, were developed and optimized using DNA extracted from formalin-fixed paraffin-embedded tumor tissues. The simplicity of the design enables POLE status assessment within 4-6 hours after DNA isolation. An interlaboratory external validation study was performed to determine the practical feasibility of this assay.RESULTSCutoffs for POLE wild-type, POLE-mutant, equivocal, and failed results were predefined on the basis of a subset of POLE mutants and POLE wild-types for the internal and external validation. For equivocal cases, additional DNA sequencing is recommended. Performance in 282 EC cases, of which 99 were POLE-mutated, demonstrated an overall accuracy of 98.6% (95% CI, 97.2 to 99.9), a sensitivity of 95.2% (95% CI, 90.7 to 99.8), and a specificity of 100%. After DNA sequencing of 8.8% equivocal cases, the final sensitivity and specificity were 96.0% (95% CI, 92.1 to 99.8) and 100%. External validation confirmed feasibility and accuracy.CONCLUSIONQPOLE is a qPCR assay that is a quick, simple, and reliable alternative for DNA sequencing. QPOLE detects all pathogenic variants in the exonuclease domain of the POLE gene. QPOLE will make low-cost POLE-testing available for all women with EC around the globe.