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Cost-effectiveness of programmed cell death ligand 1 testing and tumor mutational burden testing of immune checkpoint inhibitors for advanced non-small cell lung cancer

机译:编程细胞死亡配体的成本效益1检测和肿瘤突变检测免疫检查点抑制剂用于晚期非小细胞肺癌

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摘要

To the Editor: Worldwide, lung cancer, particularly non-small cell lung cancer (NSCLC), is the leading cause of tumor-related death. Cost-effectiveness analysis show no economic benefits for advanced NSCLC patients over chemotherapy.[1] Furthermore, tests such as programmed cell death ligand 1 (PD-L1) and tumor mutational burden (TMB) tests, evaluated via immunohistochemical methods and next-generation sequencing, respectively, are widely used for screening potential beneficiaries of immune checkpoint inhibitors (ICIs). However, these two methods have different predictive values, making their comprehensive evaluation the focus of the current controversy.
机译:向编辑:全球,肺癌,特别是非小细胞肺癌(NSCLC),是肿瘤相关死亡的主要原因。成本效益分析显示出在化疗中的高级NSCLC患者的经济效益。[1]此外,通过免疫组织化学方法和下一代测序分别评估的诸如编程细胞死亡配体1(PD-L1)和肿瘤突变负荷(TMB)试验的试验广泛用于筛选免疫检查点抑制剂(ICIS)的潜在受益者。然而,这两种方法具有不同的预测值,使其综合评价目前的争论的重点。

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