Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories

نویسندگان

  • Margherita Perricone
  • Francesca Palandri
  • Emanuela Ottaviani
  • Mario Angelini
  • Laura Bagli
  • Enrica Bellesia
  • Meris Donati
  • Donato Gemmati
  • Patrizia Zucchini
  • Stefania Mancini
  • Valentina Marchica
  • Serena Trubini
  • Giovanna De Matteis
  • Silvia Di Zacomo
  • Mosè Favarato
  • Annamaria Fioroni
  • Caterina Bolzonella
  • Giorgia Maccari
  • Filippo Navaglia
  • Daniela Gatti
  • Luisa Toffolatti
  • Linda Orlandi
  • Vèronique Laloux
  • Marco Manfrini
  • Piero Galieni
  • Barbara Giannini
  • Alessia Tieghi
  • Sara Barulli
  • Maria Luisa Serino
  • Monica Maccaferri
  • Anna Rita Scortechini
  • Nicola Giuliani
  • Daniele Vallisa
  • Massimiliano Bonifacio
  • Patrizia Accorsi
  • Cristina Salbe
  • Vinicio Fazio
  • Milena Gusella
  • Eleonora Toffoletti
  • Marzia Salvucci
  • Mirija Svaldi
  • Filippo Gherlinzoni
  • Francesca Cassavia
  • Francesco Orsini
  • Giovanni Martinelli
چکیده

To date, a plenty of techniques for the detection of JAK2V617F is used over different laboratories, with substantial differences in specificity and sensitivity. Therefore, to provide reliable and comparable results, the standardization of molecular techniques is mandatory.A network of 19 centers was established to 1) evaluate the inter- and intra-laboratory variability in JAK2V617F quantification, 2) identify the most robust assay for the standardization of the molecular test and 3) allow consistent interpretation of individual patient analysis results. The study was conceived in 3 different rounds, in which all centers had to blindly test DNA samples with different JAK2V617F allele burden (AB) using both quantitative and qualitative assays.The positivity of samples with an AB < 1% was not detected by qualitative assays. Conversely, laboratories performing the quantitative approach were able to determine the expected JAK2V617F AB. Quantitative results were reliable across all mutation loads with moderate variability at low AB (0.1 and 1%; CV = 0.46 and 0.77, respectively). Remarkably, all laboratories clearly distinguished between the 0.1 and 1% mutated samples.In conclusion, a qualitative approach is not sensitive enough to detect the JAK2V617F mutation, especially at low AB. On the contrary, the ipsogen JAK2 MutaQuant CE-IVD kit resulted in a high, efficient and sensitive quantification detection of all mutation loads. This study sets the basis for the standardization of molecular techniques for JAK2V617F determination, which will require the employment of approved operating procedures and the use of certificated standards, such as the recent WHO 1st International Reference Panel for Genomic JAK2V617F.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2017