Impact of tumor mutational burden on checkpoint inhibitor drug eligibility and outcomes across racial groups.

Impact of tumor mutational burden on checkpoint inhibitor drug eligibility and outcomes across racial groups.
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DOI:
10.1136/jitc-2021-003683
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发表时间:
2021-11
影响因子:
10.9
通讯作者:
Morris LGT
Morris LGT
中科院分区:
医学2区
文献类型:
--
作者:
Hsiehchen D;Espinoza M;Valero C;Ahn C;Morris LGT

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FDA批准用于肿瘤突变负荷(TMB)至少为10 mut/Mb的癌症的免疫检查点抑制剂,旨在通过广泛扩大治疗资格来减少医疗保健差异。在具有可用基因组和种族数据的39,400例患者的队列中,基于当前批准的临界值,黑人和亚洲患者在多种类型的恶性肿瘤中不太可能患有TMB高癌症。降低TMB阈值优先增加了少数患者接受免疫检查点抑制剂治疗的资格,同时保留了免疫检查点抑制剂治疗患者队列中治疗获益的预测值。这项研究强调了TMB高癌症在种族群体之间的不同分布,并为制定更合理的免疫检查点抑制剂资格标准提供了指导。
The FDA approval of immune checkpoint inhibitors for cancers with tumor mutation burden (TMB) of at least 10 mut/Mb is postulated to reduce healthcare disparities by broadly expanding treatment eligibility. In a cohort of 39,400 patients with available genomic and race data, black and Asian patients were less likely to have TMB-high cancers in multiple types of malignancies based on the currently approved cut-off. Decreasing TMB thresholds preferentially increased the eligibility of minority patients for immune checkpoint inhibitors while retaining predictive value of treatment benefit in a cohort of immune checkpoint inhibitor treated patients. This study highlights differing distributions of TMB-high cancers between racial groups and provides guidance in developing more rational eligibility criteria for immune checkpoint inhibitors.
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