Cargando…

Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials

BACKGROUND: Inhibitors targeting programmed cell death 1 (PD-1) and programmed death-ligand 1 (PD-L1) have unprecedented effects in cancer treatment. However, the objective response rates (ORRs), progression-free survival (PFS), and overall survival (OS) of PD-1/PD-L1 blockade monotherapy have not b...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Bin, Zhao, Hong, Zhao, Jiaxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366397/
https://www.ncbi.nlm.nih.gov/pubmed/32728392
http://dx.doi.org/10.1177/1758835920937612
_version_ 1783560211776143360
author Zhao, Bin
Zhao, Hong
Zhao, Jiaxin
author_facet Zhao, Bin
Zhao, Hong
Zhao, Jiaxin
author_sort Zhao, Bin
collection PubMed
description BACKGROUND: Inhibitors targeting programmed cell death 1 (PD-1) and programmed death-ligand 1 (PD-L1) have unprecedented effects in cancer treatment. However, the objective response rates (ORRs), progression-free survival (PFS), and overall survival (OS) of PD-1/PD-L1 blockade monotherapy have not been systematically evaluated. METHODS: We searched Embase, PubMed, and Cochrane database from inception to July 2019 for prospective clinical trials on single-agent PD-1/PD-L1 antibodies (avelumab, atezolizumab, durvalumab, cemiplimab, pembrolizumab, and nivolumab) with information regarding ORR, PFS, and OS. RESULTS: Totally, 28,304 patients from 160 perspective trials were included. Overall, 4747 responses occurred in 22,165 patients treated with PD-1/PD-L1 monotherapy [ORR, 20.21%; 95% confidence interval (CI), 18.34–22.15%]. Compared with conventional therapy, PD-1/PD-L1 blockade immunotherapy was associated with more tumor responses (odds ratio, 1.98; 95% CI, 1.52–2.57) and better OS [hazard ratio (HR), 0.75; 95% CI, 0.67–0.83]. The ORRs varied significantly across cancer types and PD-L1 expression status. Line of treatment, clinical phase and drug target also impacted the response rates in some tumors. A total of 2313 of 9494 PD-L1 positive patients (ORR, 24.39%; 95% CI, 22.29–26.54%) and 456 of 4215 PD-L1 negative patients (ORR, 10.34%; 95% CI, 8.67–12.14%) achieved responses. For PD-L1 negative patients, the ORR (odds ratio, 0.92; 95% CI, 0.70–1.20) and PFS (HR, 1.15; 95% CI, 0.87–1.51) associated with immunotherapy and conventional treatment were similar. However, PD-1/PD-L1 blockade monotherapy decreased the risk of death in both PD-L1 positive (HR, 0.66; 95% CI, 0.60–0.72) and PD-L1 negative (HR, 0.86; 95% CI, 0.74–0.99) patients compared with conventional therapy. CONCLUSION: The efficacies associated with PD-1/PD-L1 monotherapy vary significantly across cancer types and PD-L1 expression. This comprehensive summary of clinical benefit from immunotherapy in cancer patients provides an important guide for clinicians.
format Online
Article
Text
id pubmed-7366397
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-73663972020-07-28 Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials Zhao, Bin Zhao, Hong Zhao, Jiaxin Ther Adv Med Oncol Meta-Analysis BACKGROUND: Inhibitors targeting programmed cell death 1 (PD-1) and programmed death-ligand 1 (PD-L1) have unprecedented effects in cancer treatment. However, the objective response rates (ORRs), progression-free survival (PFS), and overall survival (OS) of PD-1/PD-L1 blockade monotherapy have not been systematically evaluated. METHODS: We searched Embase, PubMed, and Cochrane database from inception to July 2019 for prospective clinical trials on single-agent PD-1/PD-L1 antibodies (avelumab, atezolizumab, durvalumab, cemiplimab, pembrolizumab, and nivolumab) with information regarding ORR, PFS, and OS. RESULTS: Totally, 28,304 patients from 160 perspective trials were included. Overall, 4747 responses occurred in 22,165 patients treated with PD-1/PD-L1 monotherapy [ORR, 20.21%; 95% confidence interval (CI), 18.34–22.15%]. Compared with conventional therapy, PD-1/PD-L1 blockade immunotherapy was associated with more tumor responses (odds ratio, 1.98; 95% CI, 1.52–2.57) and better OS [hazard ratio (HR), 0.75; 95% CI, 0.67–0.83]. The ORRs varied significantly across cancer types and PD-L1 expression status. Line of treatment, clinical phase and drug target also impacted the response rates in some tumors. A total of 2313 of 9494 PD-L1 positive patients (ORR, 24.39%; 95% CI, 22.29–26.54%) and 456 of 4215 PD-L1 negative patients (ORR, 10.34%; 95% CI, 8.67–12.14%) achieved responses. For PD-L1 negative patients, the ORR (odds ratio, 0.92; 95% CI, 0.70–1.20) and PFS (HR, 1.15; 95% CI, 0.87–1.51) associated with immunotherapy and conventional treatment were similar. However, PD-1/PD-L1 blockade monotherapy decreased the risk of death in both PD-L1 positive (HR, 0.66; 95% CI, 0.60–0.72) and PD-L1 negative (HR, 0.86; 95% CI, 0.74–0.99) patients compared with conventional therapy. CONCLUSION: The efficacies associated with PD-1/PD-L1 monotherapy vary significantly across cancer types and PD-L1 expression. This comprehensive summary of clinical benefit from immunotherapy in cancer patients provides an important guide for clinicians. SAGE Publications 2020-07-16 /pmc/articles/PMC7366397/ /pubmed/32728392 http://dx.doi.org/10.1177/1758835920937612 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Meta-Analysis
Zhao, Bin
Zhao, Hong
Zhao, Jiaxin
Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials
title Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials
title_full Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials
title_fullStr Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials
title_full_unstemmed Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials
title_short Efficacy of PD-1/PD-L1 blockade monotherapy in clinical trials
title_sort efficacy of pd-1/pd-l1 blockade monotherapy in clinical trials
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366397/
https://www.ncbi.nlm.nih.gov/pubmed/32728392
http://dx.doi.org/10.1177/1758835920937612
work_keys_str_mv AT zhaobin efficacyofpd1pdl1blockademonotherapyinclinicaltrials
AT zhaohong efficacyofpd1pdl1blockademonotherapyinclinicaltrials
AT zhaojiaxin efficacyofpd1pdl1blockademonotherapyinclinicaltrials