Mansfield Aaron S, Brown Rebecca J, Sammon Cormac, Daumont Melinda J, McKenna Mike, Sanzari Jenine K, Forde Patrick M
Division of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
PHMR Ltd., Berkeley Works, London, United Kingdom.
JTO Clin Res Rep. 2022 Mar 22;3(5):100315. doi: 10.1016/j.jtocrr.2022.100315. eCollection 2022 May.
Given the emergence of combination of programmed cell death protein-1 and CTLA4 pathway blockade as effective treatment options in malignant pleural mesothelioma (MPM), there is interest in the extent to which programmed death-ligand 1 (PD-L1) expression may be prognostic of clinical outcomes and predictive of response to anti-programmed death (ligand) 1 (PD-[L]1) therapies.
MEDLINE and EMBASE electronic databases were searched until November 4, 2020. English-language randomized trials and observational studies that reported clinical outcomes and PD-L1 expression in adult patients (>18 or >20 y) with MPM were included. Forest plots were used to descriptively summarize clinical outcome data across studies.
A total of 29 publications were identified providing data on the research question. Among the studies in which anti-PD-(L)1 therapies were not specified to have been used, 63% (10 of 16) found patients with tumors expressing PD-L1 (typically >1%) to have poorer survival than those with tumors expressing lower levels of PD-L1. Among the studies in which anti-PD-(L)1 therapies were used, 83% (five of six) did not reveal an association between survival and PD-L1 tumor expression. The single study directly comparing outcomes between those treated and untreated with anti-PD-(L)1 therapies across different PD-L1 cutoffs did not identify any differences between the groups.
The quality and consistency of the existing evidence base are currently insufficient to draw conclusions regarding a prognostic or predictive role of PD-L1 in MPM. Furthermore, high-quality studies on this topic are required to support the use of PD-L1 as a biomarker in MPM.
鉴于程序性细胞死亡蛋白1与细胞毒性T淋巴细胞相关抗原4通路阻断联合疗法已成为恶性胸膜间皮瘤(MPM)的有效治疗选择,人们关注程序性死亡配体1(PD-L1)表达在多大程度上可预测临床结局以及对抗程序性死亡(配体)1(PD-[L]1)疗法的反应。
检索MEDLINE和EMBASE电子数据库至2020年11月4日。纳入报告MPM成年患者(>18岁或>20岁)临床结局和PD-L1表达的英文随机试验和观察性研究。采用森林图对各研究的临床结局数据进行描述性总结。
共识别出29篇提供有关该研究问题数据的出版物。在未明确使用抗PD-(L)1疗法的研究中,63%(16项中的10项)发现肿瘤表达PD-L1(通常>1%)的患者生存率低于肿瘤表达较低水平PD-L1的患者。在使用抗PD-(L)1疗法的研究中,83%(6项中的5项)未发现生存率与PD-L1肿瘤表达之间存在关联。唯一一项直接比较不同PD-L1临界值下接受和未接受抗PD-(L)1疗法患者结局的研究未发现两组之间存在任何差异。
目前现有证据基础的质量和一致性不足以就PD-L1在MPM中的预后或预测作用得出结论。此外,需要高质量的关于该主题的研究来支持将PD-L1用作MPM的生物标志物。