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Assessing HER-2 status in fresh frozen and archival cytological samples obtained by fine needle aspiration cytology.

机译:评估通过细针穿刺细胞学获得的新鲜冷冻和档案细胞学样品中的HER-2状态。

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A. R. Tomas, M. J. Praca, R. Fonseca, S. Andre and E. Mendonca Assessing HER-2 status in fresh frozen and archival cytological samples obtained by fine needle aspiration cytologyDetermination of HER-2 status is an essential prerequisite in considering a patient's eligibility for anti-HER-2 therapy; few studies have focused on its evaluation on cytological material. We present a new method of assessing HER-2 status on cytological samples, by fluorescence in situ hybridization (FISH) with an automated detection system, using fresh frozen (FF) and May-Grunwald-Giemsa (MGG) stained smears, and we evaluate the reliability of HER-2 determination on fine needle aspiration cytology (FNAC). The pre-treatment protocol for FF smears is easier and faster than for MGG stained slides. However, with the described procedure, FISH is also feasible on archival MGG stained slides. We conclude that with this method, cytological samples obtained by FNAC, either FF or MGG, are a reliable option for assessing HER-2 status.
机译:AR Tomas,MJ Praca,R.Fonseca,S.Andre和E.Mendonca评估通过细针穿刺细胞学获得的新鲜冷冻和档案细胞学样品中的HER-2状况确定HER-2状况的确定是考虑患者是否合格的重要前提抗HER-2疗法;很少有研究集中在对细胞学材料的评估上。我们提出了一种新方法,通过使用新鲜冷冻(FF)和May-Grunwald-Giemsa(MGG)染色涂片的自动检测系统,通过荧光原位杂交(FISH),通过荧光原位杂交(FISH)来评估细胞学样品上的HER-2状态,并且我们评估了HER-2测定对细针穿刺细胞学(FNAC)的可靠性。 FF涂片的预处理方案比MGG染色的载玻片更容易,更快。但是,使用上述程序,FISH在存档的MGG染色玻片上也是可行的。我们得出的结论是,使用这种方法,通过FNAC获得的细胞学样本(FF或MGG)是评估HER-2状态的可靠选择。

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