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肿瘤突变负荷分析靶向下一代测序 panel 的验证:Onconetwork 免疫肿瘤学联盟的研究结果。

Validation of a Targeted Next-Generation Sequencing Panel for Tumor Mutation Burden Analysis: Results from the Onconetwork Immuno-Oncology Consortium.

机构信息

Cell Biology and Biotherapy Unit, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Naples, Italy.

Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.

出版信息

J Mol Diagn. 2021 Jul;23(7):882-893. doi: 10.1016/j.jmoldx.2021.04.008. Epub 2021 May 6.

DOI:10.1016/j.jmoldx.2021.04.008
PMID:33964449
Abstract

Tumor mutation burden (TMB) is evaluated as a biomarker of response to immunotherapy. We present the efforts of the Onconetwork Immuno-Oncology Consortium to validate a commercial targeted sequencing test for TMB calculation. A three-phase study was designed to validate the Oncomine Tumor Mutational Load (OTML) assay at nine European laboratories. Phase 1 evaluated reproducibility and accuracy on seven control samples. In phase 2, six formalin-fixed, paraffin-embedded samples tested with FoundationOne were reanalyzed with the OTML panel to evaluate concordance and reproducibility. Phase 3 involved analysis of 90 colorectal cancer samples with known microsatellite instability (MSI) status to evaluate TMB and MSI association. High reproducibility of TMB was demonstrated among the sites in the first and second phases. Strong correlation was also detected between mean and expected TMB in phase 1 (r = 0.998) and phase 2 (r = 0.96). Detection of actionable mutations was also confirmed. In colorectal cancer samples, the expected pattern of MSI-high/high-TMB and microsatellite stability/low-TMB was present, and gene signatures produced by the panel suggested the presence of a POLE mutation in two samples. The OTML panel demonstrated robustness and reproducibility for TMB evaluation. Results also suggest the possibility of using the panel for mutational signatures and variant detection. Collaborative efforts between academia and companies are crucial to accelerate the translation of new biomarkers into clinical research.

摘要

肿瘤突变负担 (TMB) 被评估为免疫治疗反应的生物标志物。我们介绍了 Onconetwork 肿瘤免疫联盟努力验证一种用于 TMB 计算的商业靶向测序测试的情况。该研究设计了三个阶段,旨在验证九家欧洲实验室的 Oncomine 肿瘤突变负荷 (OTML) 检测。第一阶段评估了七个对照样本的重现性和准确性。在第二阶段,使用 FoundationOne 检测的六个福尔马林固定、石蜡包埋样本与 OTML 面板重新分析,以评估一致性和重现性。第三阶段涉及分析 90 个已知微卫星不稳定 (MSI) 状态的结直肠癌样本,以评估 TMB 和 MSI 关联。第一阶段和第二阶段的站点都显示出 TMB 的高度重现性。在第一阶段 (r = 0.998) 和第二阶段 (r = 0.96) 还检测到平均和预期 TMB 之间的强相关性。还证实了可操作突变的检测。在结直肠癌样本中,存在 MSI-高/高-TMB 和微卫星稳定性/低-TMB 的预期模式,面板产生的基因特征表明两个样本中存在 POLE 突变。OTML 面板在 TMB 评估方面表现出稳健性和重现性。结果还表明,该面板可能用于突变特征和变体检测。学术界和公司之间的合作对于加速新生物标志物转化为临床研究至关重要。

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引用本文的文献

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Explor Target Antitumor Ther. 2024;5(3):495-507. doi: 10.37349/etat.2024.00231. Epub 2024 May 23.
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High Tumor Mutation Burden Is Associated with Poor Clinical Outcome in EGFR-Mutated Lung Adenocarcinomas Treated with Targeted Therapy.在接受靶向治疗的表皮生长因子受体(EGFR)突变型肺腺癌中,高肿瘤突变负荷与不良临床结局相关。
Biomedicines. 2022 Aug 29;10(9):2109. doi: 10.3390/biomedicines10092109.