Abstract 4221: Development and evaluation of cell line-derived FFPE reference material for MSI assay validation

T. Matsusaka, Eva-Maria Surmann, Sian Constantine, H. Child, J. A. Wickenden
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Abstract

Microsatellite Instability (MSI) is defined by variance in the repeat count of microsatellite motifs and occurs in cells that are deficient in one or more mismatch repair proteins. MSI is present in varying cancer types, but is most commonly found in colorectal, gastric and endometrial cancer. Patients with early stage colorectal cancers that display MSI have a better prognosis and show a better response to chemotherapy compared to those with microsatellite stable tumors. MSI alongside additional markers such as tumor mutational burden is also a positive predictive biomarker for immune checkpoint inhibition Identification of MSI tumors in the diagnostic laboratory is traditionally performed by fluorescent multiplex PCR, evaluating the microsatellite length of two mononucleotide repeats and three dinucleotide repeats (recommended NCI Panel) or a commercially available kit, consisting of five mononucleotide markers alongside IHC staining for the four MMR proteins MSH2, MSH6, MLH1, and PMS2. With the increase in MSI testing related to the recent FDA approval of Keytruda ® , several companies and laboratories are now developing newer and better PCR-based and next-generation sequencing assays to assess MSI. To control for error, we have developed a pair of cell line-derived MSI/MSS reference samples covering the most commonly used MSI biomarkers. MSI/MSS cell lines were mixed at biologically-relevant ratios and processed into FFPE to serve as a whole-process control. Our data support the suitability of this material on a variety of different platforms and with a high degree of consistency throughout various FFPE batches. In conclusion, our cell line-derived reference samples represent a commutable control to support MSI assay development and validation. Citation Format: Takahiro Matsusaka, Eva-Maria Surmann, Sian Constantine, Hannah Child, Julie Wickenden. Development and evaluation of cell line-derived FFPE reference material for MSI assay validation [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 4221.
摘要4221:细胞系来源的FFPE标准物质的开发和评价,用于MSI检测验证
微卫星不稳定性(Microsatellite Instability, MSI)的定义是微卫星基序重复计数的变化,发生在缺乏一种或多种错配修复蛋白的细胞中。MSI存在于各种类型的癌症中,但最常见于结直肠癌、胃癌和子宫内膜癌。与微卫星稳定肿瘤患者相比,出现MSI的早期结直肠癌患者预后更好,对化疗的反应也更好。MSI与其他标志物(如肿瘤突变负担)一起,也是免疫检查点抑制的阳性预测生物标志物。在诊断实验室中,MSI肿瘤的鉴定传统上是通过荧光多重PCR进行的,评估两个单核苷酸重复序列和三个二核苷酸重复序列的微卫星长度(推荐NCI小组)或市购试剂盒。由五种单核苷酸标记组成,并对四种MMR蛋白MSH2、MSH6、MLH1和PMS2进行免疫组化染色。随着最近FDA批准Keytruda®的MSI检测的增加,一些公司和实验室正在开发更新更好的基于pcr和下一代测序的检测方法来评估MSI。为了控制误差,我们开发了一对细胞系衍生的MSI/MSS参考样品,涵盖了最常用的MSI生物标志物。MSI/MSS细胞系按生物学相关比例混合,加工成FFPE作为整个过程的对照。我们的数据支持该材料在各种不同平台上的适用性,并且在各种FFPE批次中具有高度的一致性。总之,我们的细胞系衍生的参考样品代表了一种可交换的对照,以支持MSI分析的开发和验证。引文格式:Takahiro Matsusaka, Eva-Maria Surmann, Sian Constantine, Hannah Child, Julie Wickenden。开发和评价细胞系来源的FFPE标准物质用于MSI测定验证[摘要]。摘自:2019年美国癌症研究协会年会论文集;2019年3月29日至4月3日;亚特兰大,乔治亚州。费城(PA): AACR;癌症杂志,2019;79(13增刊):4221。
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