首页> 美国卫生研究院文献>Cancers >Reply to Comment on Jilkova Z.M.; et al. Predictive Factors for Response to PD-1/PD-L1 Checkpoint Inhibition in the Field of Hepatocellular Carcinoma: Current Status and Challenges
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Reply to Comment on Jilkova Z.M.; et al. Predictive Factors for Response to PD-1/PD-L1 Checkpoint Inhibition in the Field of Hepatocellular Carcinoma: Current Status and Challenges

机译:回复JilkovaZ.M评论。等等。对PD-1 / PD-L1检查点抑制在肝细胞癌领域的预测因素:当前地位和挑战

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摘要

We appreciate the comments made on our review paper focused on possible predictive factors for responses to PD-1/PD-L1 checkpoint inhibitors in the field of hepatocellular carcinoma [1]. We fully agree that the statement “Certainly, high tumor mutational burden and neoantigen load have been noted to predict the response to immunotherapies, including anti-PD-1 therapy (higher objective response rate and/or prolonged survival) in melanoma, non-small-cell lung carcinoma” is not supported by the given reference of Topalian et al. for the year 2012 [2]. As mentioned in the comment, the correct reference is Goodman et al.’s work from 2017 [3], cited in our original review as reference number 60, where the authors demonstrated a linear correlation between higher tumor mutational burden and better outcome parameters based on 151 immunotherapy-treated patients. In addition, our statement can be supported by a recent meta-analysis from Kim et al. 2019 [4], which focused on the tumor mutational burden and efficacy of immune checkpoint inhibitors in more than 5000 patients with various advanced cancer types. The authors showed that the patients with high tumor mutational burden have significantly higher objective response rates and prolonged survival as compared to patients with low tumor mutational burden undergoing immune checkpoint inhibitor treatment.
机译:感谢我们对我们的审核文件所作的评论,重点是可能的预测因素,以应对肝细胞癌领域的PD-1 / PD-L1检查点抑制剂的可能预测因素[1]。我们完全同意声明“当然,高肿瘤突变负担和新洲洲荷兰载荷预测,预测对免疫疗法的反应,包括黑素瘤的抗PD-1治疗(更高的客观反应率和/或延长的存活率),非小 - 特定的Topalial等人的参考不支持-Cell肺癌。 2012年[2]。如评论所述,正确的参考是Goodman等人。从2017年的工作[3],在我们的原始审查中被引用为参考号60,作者在其中展示了肿瘤突变负担和基于更好的结果参数之间的线性相关性在151例免疫疗法治疗的患者。此外,我们的陈述可以通过Kim等人的最近的Meta分析来支持。 2019 [4],其重点是肿瘤突变负担和免疫检查点抑制剂在5000多名各种先进癌症类型患者中的疗效。作者表明,与肿瘤突变负担抑制剂治疗的低肿瘤突变负担患者相比,肿瘤突变负担患者具有明显较高的客观反应率和延长的存活。

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