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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

5399 - Clinical and molecular characteristics associated with efficacy of PD-1/PD-L1 inhibitors for solid tumors: A Meta-analysis

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Topics

Pathology/Molecular Biology

Tumour Site

Presenters

Min Peng

Citation

Annals of Oncology (2018) 29 (suppl_8): viii400-viii441. 10.1093/annonc/mdy288

Authors

M. Peng1, Y. Weng2, Y. Yao1, Q. Song2

Author affiliations

  • 1 Oncology, Renmin Hospital of Wuhan University, 430060 - Wuhan/CN
  • 2 Cancer Center, enmin Hospital of Wuhan University, 430060 - wuhan/CN

Resources

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Abstract 5399

Background

In the new era of precision medicine, identifying clinical or molecular factors that predict benefit of immune checkpoint inhibitors is crucial to prevent patients from autoimmune adverse effects and high cost of such agents.

Methods

We conducted this meta-analysis on the basis of the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-analyses) statement. Two reviews independently completed a search of PubMed and Web of science to identify relevant clinical trials. The search was conducted using keywords “nivolumab”, “pembrolizumab”, “atezolizumab” and “immune checkpoint”. The search was limited to randomized controlled trails (RCTs) published in English.

Results

Eleven eligible studies, including 5,663 patients, were included in this meta-analysis. In our analysis, PD-1/PD-L1 inhibitor was associated with a 31% reduction in the risk of death (HR = 0.69; 95%CI, 0.64-0.74; P < 0.00001). In subgroup analysis, patients got overall survival (OS) benefit from PD-1/PD-L1 inhibitors regardless of PD-L1 expression, and a dose effect relationship between expression of PD-L1 and OS benefit from PD-1/PD-L1 inhibitors was observed (Interaction, P < 0.00001). Patients with smoking history achieved greater OS benefits (HR = 0.69, 95% CI 0.61-0.77; P < 0.00001) than never smoker (HR = 0.88, 95% CI 0.70-1.11; P = 0.28). Compared with second or later line treatment, there was better OS benefits in first line treatment subgroup (Interaction, P = 0.02). The OS benefits were similar according to age (Interaction, P = 0.74), sex (Interaction, P = 0.43), performance status (Interaction, P = 0.68), central nervous system (CNS) metastasis (Interaction, P = 0.59), tumor histology (Interaction, P = 0.64) and treatment type (Interaction, P = 0.36).

Conclusions

In conclusion, PD-L1 expression, smoking status and line of treatment were potential biomarkers for PD-1/PD-L1 inhibitors. Besides, patients > 75 years of age might not get OS benefits from this treatment. These results may improve treatment strategies and patient selection for PD-1/PD-L1 inhibitors.

Legal entity responsible for the study: Y. Weng.

Clinical trial identification

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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