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. 2020 Feb;11(2):408-414.
doi: 10.1111/1759-7714.13284. Epub 2019 Dec 16.

Efficacy of immune checkpoint inhibitors according to PD-L1 tumor proportion scores in non-small cell lung cancer

Affiliations

Efficacy of immune checkpoint inhibitors according to PD-L1 tumor proportion scores in non-small cell lung cancer

Seongho Park et al. Thorac Cancer. 2020 Feb.

Abstract

Background: We correlated the tumor proportion score (TPS) of programmed cell death ligand 1 (PD-L1, SP263 or 22C3) expression with the disease control rate (DCR, partial remission and stable disease), and progression free survival (PFS) after nivolumab or pembrolizumab treatment.

Methods: A total of 70 case records (55 males, 15 females) of patients with non-small cell lung cancer (NSCLC, 46 adenocarcinoma, 22 squamous cell carcinoma, and two others) were reviewed. The PD-L1 expressions were divided into High (SP263 ≥ 30%, 22C3 ≥ 80%) and Low groups (SP263 < 30%, 22C3 < 80%). In the combined analysis, the PD-L1 group was defined as High if either of the two stains was classified as High and defined as Low if both stains were classified as Low.

Results: Among the patients treated with nivolumab (n = 37), the SP263 High group showed higher DCR compared to the SP263 Low group (52.6% vs. 11.1%, P = 0.024). In patients treated with pembrolizumab (n = 33), no significant difference in DCR and PFS according to PD-L1 expression was observed. In the combined analysis (n = 36), patients in the PD-L1 High group showed significantly higher DCRs than those in the PD-L1 Low group (56.1% vs. 24.1%, P = 0.028). PFS was significantly longer in the PD-L1 High group than in the Low group (medians 4.1 vs. 1.6 months, respectively, P = 0.04).

Conclusion: A high expression level of PD-L1 was correlated with a significantly higher DCR and longer PFS in NSCLC patients treated with nivolumab or pembrolizumab.

Keywords: Nivolumab; non-small cell lung cancer; pembrolizumab; programmed cell death ligand 1.

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Figures

Figure 1
Figure 1
Comparison (a) and correlation (b) of PD‐L1 (SP263 and 22C3) expression in 36 patients tested with both antibodies. The data are presented as median and interquartile range. TPS, tumor proportion score. formula image Pembrolizumab; formula image Nivolumab.
Figure 2
Figure 2
The overall response rate (a) and disease control rate (b) of PD‐L1 High (black) and Low (grey) groups of patients treated with nivolumab (n = 37), pembrolizumab (n = 33), and the combination (n = 36). formula image High, formula image Low.
Figure 3
Figure 3
Progression‐free survival in PD‐L1 High and Low groups of patients treated with nivolumab (a, n = 37), pembrolizumab (b, n = 33), the combination (c, n = 36), and overall survival (d, n = 36), strata formula image PD‐L1=High formula imagePD‐L1=Low.

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