Cargando…

An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic

Background: There are limited clinical data comparing extended dosing (ED) versus standard dosing (SD) of pembrolizumab for metastatic non-small-cell lung cancer. Methods: This retrospective study included patients with metastatic non-small-cell lung cancer and PD-L1 tumor proportion score ≥50% trea...

Descripción completa

Detalles Bibliográficos
Autores principales: Moffat, Gordon Taylor, Hanna, Lilian, Hopman, Wilma, Fung, Andrea S, Gaudreau, Pierre-Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340130/
https://www.ncbi.nlm.nih.gov/pubmed/37431608
http://dx.doi.org/10.2217/imt-2022-0257
_version_ 1785072005088804864
author Moffat, Gordon Taylor
Hanna, Lilian
Hopman, Wilma
Fung, Andrea S
Gaudreau, Pierre-Olivier
author_facet Moffat, Gordon Taylor
Hanna, Lilian
Hopman, Wilma
Fung, Andrea S
Gaudreau, Pierre-Olivier
author_sort Moffat, Gordon Taylor
collection PubMed
description Background: There are limited clinical data comparing extended dosing (ED) versus standard dosing (SD) of pembrolizumab for metastatic non-small-cell lung cancer. Methods: This retrospective study included patients with metastatic non-small-cell lung cancer and PD-L1 tumor proportion score ≥50% treated with one or more cycles of single-agent pembrolizumab with SD or ED from January 2018 to December 2020. Results: A higher proportion of patients were alive in the ED group (vs SD) at 6 months (94 vs 51%), 12 months (94 vs 33%) and data cutoff (94 vs 26%) (p < 0.001 for all). The rate (44 vs 32%; p = 0.407) and severity of grade ≥3 immune-related adverse events were similar (50 vs 52%); however, ED patients more frequently discontinued treatment due to toxicity (45 vs 15%; p < 0.001). Conclusion: A greater proportion of ED patients were alive at data cutoff, and the rate and severity of immune-related adverse events were similar between groups.
format Online
Article
Text
id pubmed-10340130
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Future Medicine Ltd
record_format MEDLINE/PubMed
spelling pubmed-103401302023-07-14 An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic Moffat, Gordon Taylor Hanna, Lilian Hopman, Wilma Fung, Andrea S Gaudreau, Pierre-Olivier Immunotherapy Research Article Background: There are limited clinical data comparing extended dosing (ED) versus standard dosing (SD) of pembrolizumab for metastatic non-small-cell lung cancer. Methods: This retrospective study included patients with metastatic non-small-cell lung cancer and PD-L1 tumor proportion score ≥50% treated with one or more cycles of single-agent pembrolizumab with SD or ED from January 2018 to December 2020. Results: A higher proportion of patients were alive in the ED group (vs SD) at 6 months (94 vs 51%), 12 months (94 vs 33%) and data cutoff (94 vs 26%) (p < 0.001 for all). The rate (44 vs 32%; p = 0.407) and severity of grade ≥3 immune-related adverse events were similar (50 vs 52%); however, ED patients more frequently discontinued treatment due to toxicity (45 vs 15%; p < 0.001). Conclusion: A greater proportion of ED patients were alive at data cutoff, and the rate and severity of immune-related adverse events were similar between groups. Future Medicine Ltd 2023-07-11 2023-05 /pmc/articles/PMC10340130/ /pubmed/37431608 http://dx.doi.org/10.2217/imt-2022-0257 Text en © 2023 Future Medicine Ltd https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Research Article
Moffat, Gordon Taylor
Hanna, Lilian
Hopman, Wilma
Fung, Andrea S
Gaudreau, Pierre-Olivier
An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic
title An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic
title_full An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic
title_fullStr An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic
title_full_unstemmed An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic
title_short An assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the COVID-19 pandemic
title_sort assessment of extended pembrolizumab dosing in advanced non-small-cell lung cancer in the covid-19 pandemic
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340130/
https://www.ncbi.nlm.nih.gov/pubmed/37431608
http://dx.doi.org/10.2217/imt-2022-0257
work_keys_str_mv AT moffatgordontaylor anassessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT hannalilian anassessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT hopmanwilma anassessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT fungandreas anassessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT gaudreaupierreolivier anassessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT moffatgordontaylor assessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT hannalilian assessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT hopmanwilma assessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT fungandreas assessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic
AT gaudreaupierreolivier assessmentofextendedpembrolizumabdosinginadvancednonsmallcelllungcancerinthecovid19pandemic