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    <title>Segeren, C.</title>
    <link>http://repub.eur.nl/res/aut/4442/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Consensus strategy to quantitate malignant cells in myeloma patients is validated in a multicenter study. Belgium-Dutch Hematology-Oncology Group (Article)</title>
      <link>http://repub.eur.nl/res/pub/9419/</link>
      <pubDate>2000-01-01T00:00:00Z</pubDate>
      <description>Recently the Belgium-Dutch Hematology-Oncology group initiated a
          multicenter study to evaluate whether myeloma patients treated with
          intensive chemotherapy benefit from additional peripheral stem cell
          transplantation. To determine treatment response accurately, we decided to
          quantitate malignant cells. To test a consensus quantitation strategy, 5
          centers independently determined the immunoglobulin heavy chain sequences
          of patient tumor cells and developed allele-specific oligonucleotides
          (ASO) and ASO-polymerase chain reaction (PCR). We compared the
          reproducibility of real-time quantitation with quantitation using limiting
          dilutions. We distributed DNA samples with a 4-log range of tumor cell
          concentrations and found average quantitation values deviating 74% and 42%
          from the input values with real-time PCR (1 center) and limiting dilutions
          (4 centers), respectively. Within single centers we found an average
          variation coefficient of 0.74, with limiting dilutions not significantly
          different from the average 0.82 center-to-center variation coefficient.
          Within a single center, real-time quantitation proved more reproducible
          (average variation coefficient, 0.36). Quantification was confirmed in 3
          patients during treatment in the protocol. This report shows that
          real-time PCR or limiting dilution assays can be used for quantitation in
          a single multicenter trial. We present a consensus strategy that allows an
          accurate comparison of quantitation data generated in independent centers.</description>
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