Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Meta-Analysis
. 2021 Jan 27;5(3):pkab012.
doi: 10.1093/jncics/pkab012. eCollection 2021 Jun.

Response Rate and Survival at Key Timepoints With PD-1 Blockade vs Chemotherapy in PD-L1 Subgroups: Meta-Analysis of Metastatic NSCLC Trials

Affiliations
Meta-Analysis

Response Rate and Survival at Key Timepoints With PD-1 Blockade vs Chemotherapy in PD-L1 Subgroups: Meta-Analysis of Metastatic NSCLC Trials

Johnathan Man et al. JNCI Cancer Spectr. .

Abstract

Background: Expression of programmed cell death ligand 1 (PD-L1) on tumor cells with or without immune cells is widely reported in clinical trials of programmed cell death receptor 1 (PD-1) blockade in metastatic non-small cell lung cancer. Various cutpoints have been studied.

Methods: We performed a systematic search of MEDLINE, EMBASE, and conference proceedings up to December 2019 for randomized and nonrandomized clinical trials of anti-PD-1 or anti-PD-L1 monotherapy in metastatic non-small cell lung cancer. We retrieved data on objective response rate (ORR), 1-year and 2-year progression-free survival (PFS), and 2-year and 3-year overall survival (OS) in various PD-L1 subgroups. Results were pooled and analyzed based on different cutpoints, with nonrandomized comparisons made with pooled chemotherapy outcomes.

Results: A total of 9810 patients in 27 studies were included. In treatment-naïve patients, benefits with PD-1 blockade over chemotherapy were seen in ORR in patients having PD-L1 50% or greater, in 2-year OS for PD-L1 1% or greater, and in 1-year PFS, 2-year PFS, and 3-year OS for unselected patients. First-line PD-1 blockade compared with chemotherapy demonstrated higher ORR, 2-year PFS, and 3-year OS if PD-L1 was 50% or greater; lower ORR, higher 2-year PFS, and similar 3-year OS if PD-L1 was 1%-49%; and lower ORR, similar 1-year PFS, and lower 2-year OS if PD-L1 was less than 1%. In previously treated patients, PD-1 blockade demonstrated similar or superior outcomes to chemotherapy in all PD-L1 subgroups.

Conclusions: PD-L1 should guide the choice of PD-1 blockade vs chemotherapy in treatment-naïve patients. In previously treated patients, PD-1 blockade provides a favorable outcome profile to chemotherapy in all PD-L1 subgroups.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Flow diagram of included and excluded studies. EGFR = epidermal growth factor receptor; ORR = objective response rate; OS = overall survival; PD-1 = programmed cell death receptor 1; PD-L1 = programmed cell death ligand 1; PFS = progression-free survival.
Figure 2.
Figure 2.
Objective response rate (ORR) of chemotherapy, or programmed cell death receptor 1 (PD-1) blockade in different programmed cell death ligand 1 (PD-L1) subgroups. A) ORR in treatment-naïve patients. B) ORR in previously treated patients. Error bars represent 95% confidence intervals for the pooled estimate.
Figure 3.
Figure 3.
One-year and 2-year progression-free survival (PFS) rates of chemotherapy, or programmed cell death receptor 1 (PD-1) blockade in different programmed cell death ligand 1 (PD-L1) subgroups. A) One-year PFS in treatment-naïve patients. B) One-year PFS in previously treated patients. C) Two-year PFS in treatment-naïve patients. D) Two-year PFS in previously treated patients. Error bars represent 95% confidence intervals for the pooled estimate.
Figure 4.
Figure 4.
Two-year and 3-year overall survival (OS) rates of chemotherapy, or programmed cell death receptor 1 (PD-1) blockade in different programmed cell death ligand 1 (PD-L1) subgroups. A) Two-year OS in treatment naïve patients. B) Two-year OS in previously treated patients. C) Three-year OS in treatment-naïve patients. D) Three-year OS in previously treated patients. Error bars represent 95% confidence intervals for the pooled estimate. PD-1 = programmed cell death receptor 1; PD-L1 = programmed cell death ligand 1.

Comment in

References

    1. Cheng T-YD, Crumb SM, Baade PD, et al.The international epidemiology of lung cancer: latest trends, disparities, and tumor characteristics. J Thorac Oncol. 2016;11(10):1653–1671. - PMC - PubMed
    1. Alexandrov LB, Nik-Zainal S, Wedge DC, et al.; Australian Pancreatic Cancer Genome Initiative. Signatures of mutational processes in human cancer. Nature. 2013;500(7463):415–421. - PMC - PubMed
    1. Hanahan D, Weinberg RA.. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646–674. - PubMed
    1. Mittal D, Gubin MM, Schreiber RD, Smyth MJ.. New insights into cancer immunoediting and its three component phases—elimination, equilibrium and escape. Curr Opin Immunol. 2014;27:16–25. - PMC - PubMed
    1. Hanna N, Johnson D, Temin S, et al.Systemic therapy for stage IV non-small-cell lung cancer: American Society of Clinical Oncology Clinical Practice Guideline update. J Clin Oncol. 2017;35(30):3484–3515. - PubMed

MeSH terms