4.7 Article

Heterogeneity in PD-L1 expression in malignant peritoneal mesothelioma with systemic or intraperitoneal chemotherapy

期刊

BRITISH JOURNAL OF CANCER
卷 124, 期 3, 页码 564-566

出版社

SPRINGERNATURE
DOI: 10.1038/s41416-020-01130-x

关键词

-

类别

资金

  1. National Institute of Health Kirschtein National Research Service (T32) Award
  2. University of Chicago, Department of Surgical Oncology

向作者/读者索取更多资源

PD-L1 expression in patients with malignant peritoneal mesothelioma is associated with germline and somatic mutations. Patients who had received prior chemotherapy showed varying levels of PD-L1 expression, with some exhibiting upregulation and others downregulation. The heterogeneity in PD-L1 expression before and after cytotoxic therapies may impact the effectiveness of immune checkpoint inhibition in this challenging disease.
Programmed death-ligand 1 (PD-L1) expression has been described in patients with malignant peritoneal mesothelioma (MPM), but treatment strategies utilising immune checkpoint inhibition are yet to be defined. Here, we examine levels of PD-L1 expression in MPM patients treated with systemic and/or intraperitoneal chemotherapy using tissue from patient tumour biopsies or resections at multiple time points. We found the mean PD-L1 expression was higher in those with a germline mutation and/or those with a higher somatic mutation burden. Moreover, PD-L1 expression was lower in patients who had received prior chemotherapy as compared to the treatment-naive cohort. Twenty patients who received chemotherapy, either systemic and/or peritoneal, between PD-L1 measurements showed marked heterogeneity. Six (30%) patients demonstrated upregulation of PD-L1, while eight (40%) demonstrated downregulation. Heterogeneity in PD-L1 expression in MPM before and after cytotoxic therapies may present an additional consideration when initiating immune checkpoint inhibition in this rare and challenging disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据