Zhang Yuanfeng, Wang Duo, Zhao Zihong, Peng Rongxue, Han Yanxi, Li Jinming, Zhang Rui
National Center for Clinical Laboratories, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing Hospital/National Center of Gerontology, Beijing, PR China.
National Center for Clinical Laboratories, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, PR China.
NPJ Precis Oncol. 2024 Jan 23;8(1):18. doi: 10.1038/s41698-024-00504-1.
Targeted panel-based tumor mutation burden (TMB) assays are widely employed to guide immunotherapy for patients with solid tumors. However, the accuracy and consistency of this method can be compromised due to the variability in technical details across different laboratories, particularly in terms of panel size, somatic mutation detection and TMB calculation rules. Currently, systematic evaluations of the impact of these technical factors on existing assays and best practice recommendations remain lacking. We assessed the performance of 50 participating panel-based TMB assays involving 38 unique methods using cell line samples. In silico experiments utilizing TCGA MC3 datasets were performed to further dissect the impact of technical factors. Here we show that the panel sizes beyond 1.04 Mb and 389 genes are necessary for the basic discrete accuracy, as determined by over 40,000 synthetic panels. The somatic mutation detection should maintain a reciprocal gap of recall and precision less than 0.179 for reliable psTMB calculation results. The inclusion of synonymous, nonsense and hotspot mutations could enhance the accuracy of panel-based TMB assay. A 5% variant allele frequency cut-off is suitable for TMB assays using tumor samples with at least 20% tumor purity. In conclusion, this multicenter study elucidates the major technical factors as sources of variability in panel-based TMB assays and proposed comprehensive recommendations for the enhancement of accuracy and consistency. These findings will assist clinical laboratories in optimizing the methodological details through bioinformatic experiments to enhance the reliability of panel-based methods.
基于靶向基因panel的肿瘤突变负荷(TMB)检测方法被广泛用于指导实体瘤患者的免疫治疗。然而,由于不同实验室技术细节的差异,特别是在基因panel大小、体细胞突变检测和TMB计算规则方面,该方法的准确性和一致性可能会受到影响。目前,对于这些技术因素对现有检测方法的影响以及最佳实践建议仍缺乏系统评估。我们使用细胞系样本评估了50种参与的基于基因panel的TMB检测方法的性能,这些方法涉及38种独特的技术。利用TCGA MC3数据集进行了计算机模拟实验,以进一步剖析技术因素的影响。我们发现,超过1.04 Mb和389个基因的基因panel大小对于基本离散准确性是必要的,这是由超过40,000个合成基因panel确定的。为了获得可靠的psTMB计算结果,体细胞突变检测应保持召回率和精确率的相互差距小于0.179。纳入同义突变、无义突变和热点突变可以提高基于基因panel的TMB检测的准确性。对于肿瘤纯度至少为20%的肿瘤样本,5%的变异等位基因频率截止值适用于TMB检测。总之,这项多中心研究阐明了基于基因panel的TMB检测中变异的主要技术因素来源,并提出了提高准确性和一致性的全面建议。这些发现将帮助临床实验室通过生物信息学实验优化方法细节,以提高基于基因panel方法的可靠性。