Smits AJ,Kummer JA,de Bruin PC,Bol M,van den Tweel JG,Seldenrijk KA,Willems SM,Offerhaus GJ,de Weger RA,van Diest PJ,Vink A
Abstract
Molecular pathology is becoming more and more important in present day pathology. A major challenge for any molecular test is its ability to reliably detect mutations in samples consisting of mixtures of tumor cells and normal cells, especially when the tumor content is low. The minimum percentage of tumor cells required to detect genetic abnormalities is a major variable. Information on tumor cell percentage is essential for a correct interpretation of the result. In daily practice, the percentage of tumor cells is estimated by pathologists on hematoxylin and eosin (H&E)-stained slides, the reliability of which has been questioned. This study aimed to determine the reliability of estimated tumor cell percentages in tissue samples by pathologists. On 47 H&E-stained slides of lung tumors a tumor area was marked. The percentage of tumor cells within this area was estimated independently by nine pathologists, using categories of 0-5%, 6-10%, 11-20%, 21-30%, and so on, until 91-100%. As gold standard, the percentage of tumor cells was counted manually. On average, the range between the lowest and the highest estimate per sample was 6.3 categories. In 33% of estimates, the deviation from the gold standard was at least three categories. The mean absolute deviation was 2.0 categories (range between observers 1.5-3.1 categories). There was a significant difference between the observers (P<0.001). If 20% of tumor cells were considered the lower limit to detect a mutation, samples with an insufficient tumor cell percentage (<20%) would have been estimated to contain enough tumor cells in 27/72 (38%) observations, possibly causing false negative results. In conclusion, estimates of tumor cell percentages on H&E-stained slides are not accurate, which could result in misinterpretation of test results. Reliability could possibly be improved by using a training set with feedback.
摘要
分子病理学在当今病理学中变得日益重要。对所有分子检测的主要挑战就是在混有肿瘤细胞和正常细胞的样本中可靠的检测到突变,特别当肿瘤细胞含量低的时候也能准确检测到突变。可检测出基因异常的最少肿瘤细胞含量是一个重要变量。肿瘤细胞的百分含量对结果的准确解释是至关重要的。日常工作中,病理学家通过HE染色切片评估肿瘤细胞百分含量,其本身的可靠性受到质疑。
本研究旨在确定病理学家估计组织样本肿瘤细胞含量的准确性。标记47例HE染色的肺癌肿瘤细胞区域。9名病理医生独立评估选定区域的肿瘤细胞的百分比,划分等级0-5%,6-10%,11-20%,21-30%.....91-100%。
人工估计肿瘤细胞的含量作为金标准。每个样本的最高和最低估计值平均相差6.3个级别。估计值中有33%偏离金标准至少3个级别。偏离的绝对均值是2.0个等级。(范围1.5-3.1)。观察者之间的差异具有统计学意义(P<0.001)如果20%的肿瘤细胞被认为是检测突变的最低值,低于20%肿瘤细胞的样本可能会被估计成含有足够肿瘤细胞的样本,在72例被观察的样本中有27例出现这种情况(比率38%),这很可能导致假阴性结果。
总之,估计HE染色切片的肿瘤细胞含量是不准确的,并且可能导致结果的错误解释。对样本含量估计的可靠性通过具有反馈的训练可能得到提高。
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