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

被引:22
|
作者
White, Michael G. [1 ]
Schulte, Jefree J. [2 ]
Xue, Lai [3 ]
Berger, Yaniv [3 ]
Schuitevoerder, Darryl [3 ]
Vining, Charles C. [3 ]
Kindler, Hedy L. [4 ]
Husain, Aliya [2 ]
Turaga, Kiran K. [3 ]
Eng, Oliver S. [3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[2] Univ Chicago, Dept Pathol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Surg, Sect Gen Surg & Surg Oncol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Med, Sect Hematol Oncol, 5841 S Maryland Ave, Chicago, IL 60637 USA
关键词
TRIAL;
D O I
10.1038/s41416-020-01130-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:564 / 566
页数:3
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