Cellular Pathology, Royal Liverpool and Broadgreen Hospitals NHS Trust, Liverpool, UK.
Center for Cancer Outcomes, North Central and North East London Cancer Alliances, UCLH, London, UK.
J Clin Pathol. 2024 Jan 18;77(2):135-139. doi: 10.1136/jcp-2022-208643.
Programmed cell death ligand 1 (PD-L1) expression, used universally to predict response of non-small cell lung cancer (NSCLC) to immune-modulating drugs, is a fragile biomarker due to biological heterogeneity and challenges in interpretation. The aim of this study was to assess current PD-L1 testing practices in the UK, which may help to define strategies to improve its reliability and consistency.
A questionnaire covering NSCLC PD-L1 testing practice was devised and members of the Association of Pulmonary Pathologists were invited to complete this online.
Of 44 pathologists identified as involved in PD-L1 testing, 32 (73%) responded. There was good consistency in practice and approach, but there was wide variability in the distribution of PD-L1 scoring. Although the proportions of scores falling into the three groups (negative, low and high) defined by the 1% and 50% 'cut-offs' (38%, 33% and 27%, respectively) reflect the general experience, the range within each group was wide at 23-70%, 10-60% and 15-36%, respectively.
There is inconsistency in the crucial endpoint of PD-L1 testing of NSCLC, the expression score that guides management. Addressing this requires formal networking of individuals and laboratories to devise a strategy for its reduction.
程序性死亡配体 1(PD-L1)表达被广泛用于预测非小细胞肺癌(NSCLC)对免疫调节药物的反应,但由于生物学异质性和解释上的挑战,它是一种脆弱的生物标志物。本研究旨在评估英国目前的 PD-L1 检测实践,这可能有助于确定提高其可靠性和一致性的策略。
设计了一份涵盖 NSCLC PD-L1 检测实践的问卷,并邀请肺病理学家协会的成员在线完成。
在确定的 44 名参与 PD-L1 检测的病理学家中,有 32 名(73%)做出了回应。实践和方法上存在很好的一致性,但 PD-L1 评分的分布存在很大的差异。虽然落入三个组(阴性、低和高)的比例反映了一般经验,分别为 38%、33%和 27%,但每个组内的范围很广,分别为 23-70%、10-60%和 15-36%。
在指导管理的 NSCLC PD-L1 检测的关键终点即表达评分上存在不一致性。解决这一问题需要个人和实验室正式建立网络,制定减少这种不一致性的策略。