Cargando…

Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189

INTRODUCTION: The aim of this study was to evaluate the efficacy of pemetrexed and platinum plus pembrolizumab by baseline tumor burden. METHODS: A total of 616 patients in the intention-to-treat population of the KEYNOTE-189 study were included in this analysis. Baseline tumor burden subgroups were...

Descripción completa

Detalles Bibliográficos
Autores principales: Gadgeel, Shirish, Gray, Jhanelle E., Rizzo, Maria Teresa, Peterson, Patrick, Kim, Jong Seok, Rodríguez-Abreu, Delvys
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667308/
https://www.ncbi.nlm.nih.gov/pubmed/36406000
http://dx.doi.org/10.1016/j.jtocrr.2022.100389
_version_ 1784831698045763584
author Gadgeel, Shirish
Gray, Jhanelle E.
Rizzo, Maria Teresa
Peterson, Patrick
Kim, Jong Seok
Rodríguez-Abreu, Delvys
author_facet Gadgeel, Shirish
Gray, Jhanelle E.
Rizzo, Maria Teresa
Peterson, Patrick
Kim, Jong Seok
Rodríguez-Abreu, Delvys
author_sort Gadgeel, Shirish
collection PubMed
description INTRODUCTION: The aim of this study was to evaluate the efficacy of pemetrexed and platinum plus pembrolizumab by baseline tumor burden. METHODS: A total of 616 patients in the intention-to-treat population of the KEYNOTE-189 study were included in this analysis. Baseline tumor burden subgroups were identified on the basis of extent of distant metastasis (M1a versus M1b), median number (≤3 versus >3) of organ systems with lesions, or symptom severity score of patient-reported lung cancer-associated symptoms (≤median versus >median). Overall survival (OS), progression-free survival (PFS), and PFS-2 were evaluated by Kaplan-Meier and univariate Cox methods. Objective response rate was analyzed using logistic regression models, and duration of response was analyzed descriptively. Efficacy outcomes were also analyzed according to the programmed death-ligand 1 expression levels. RESULTS: OS and PFS were significantly improved with pemetrexed and platinum plus pembrolizumab in all baseline tumor burden subgroups (M1a stage: OS hazard ratio [HR] = 0.54, p = 0.0037; PFS HR = 0.48, p = 0.0001; M1b stage: OS HR = 0.58, p ≤ 0.0001; PFS HR = 0.51, p ≤ 0.0001; number of organ systems with lesion ≤ 3: OS HR = 0.49, p ≤ 0.0001 PFS HR = 0.41, p ≤ 0.0001; >3: OS HR = 0.67, p = 0.0068; PFS HR = 0.59, p = 0.0001; symptom severity score ≤ median: HR = 0.51, p ≤ 0.0001; PFS HR 0.49, p ≤ 0.0001; > median: OS HR = 0.60, p = 0.0003; PFS HR = 0.48, p ≤ 0.0001). PFS2 and objective response rate were also improved with pemetrexed and platinum plus pembrolizumab in all baseline tumor burden subgroups. Efficacy outcomes were generally consistent regardless of programmed death-ligand 1 expression levels. CONCLUSIONS: Pemetrexed and platinum plus pembrolizumab were found to have relevant efficacy regardless of the extent of baseline tumor burden and the variables used to define it. These results further support pemetrexed and platinum plus pembrolizumab as the standard of care in the first-line treatment of metastatic nonsquamous NSCLC.
format Online
Article
Text
id pubmed-9667308
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-96673082022-11-17 Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189 Gadgeel, Shirish Gray, Jhanelle E. Rizzo, Maria Teresa Peterson, Patrick Kim, Jong Seok Rodríguez-Abreu, Delvys JTO Clin Res Rep Original Article INTRODUCTION: The aim of this study was to evaluate the efficacy of pemetrexed and platinum plus pembrolizumab by baseline tumor burden. METHODS: A total of 616 patients in the intention-to-treat population of the KEYNOTE-189 study were included in this analysis. Baseline tumor burden subgroups were identified on the basis of extent of distant metastasis (M1a versus M1b), median number (≤3 versus >3) of organ systems with lesions, or symptom severity score of patient-reported lung cancer-associated symptoms (≤median versus >median). Overall survival (OS), progression-free survival (PFS), and PFS-2 were evaluated by Kaplan-Meier and univariate Cox methods. Objective response rate was analyzed using logistic regression models, and duration of response was analyzed descriptively. Efficacy outcomes were also analyzed according to the programmed death-ligand 1 expression levels. RESULTS: OS and PFS were significantly improved with pemetrexed and platinum plus pembrolizumab in all baseline tumor burden subgroups (M1a stage: OS hazard ratio [HR] = 0.54, p = 0.0037; PFS HR = 0.48, p = 0.0001; M1b stage: OS HR = 0.58, p ≤ 0.0001; PFS HR = 0.51, p ≤ 0.0001; number of organ systems with lesion ≤ 3: OS HR = 0.49, p ≤ 0.0001 PFS HR = 0.41, p ≤ 0.0001; >3: OS HR = 0.67, p = 0.0068; PFS HR = 0.59, p = 0.0001; symptom severity score ≤ median: HR = 0.51, p ≤ 0.0001; PFS HR 0.49, p ≤ 0.0001; > median: OS HR = 0.60, p = 0.0003; PFS HR = 0.48, p ≤ 0.0001). PFS2 and objective response rate were also improved with pemetrexed and platinum plus pembrolizumab in all baseline tumor burden subgroups. Efficacy outcomes were generally consistent regardless of programmed death-ligand 1 expression levels. CONCLUSIONS: Pemetrexed and platinum plus pembrolizumab were found to have relevant efficacy regardless of the extent of baseline tumor burden and the variables used to define it. These results further support pemetrexed and platinum plus pembrolizumab as the standard of care in the first-line treatment of metastatic nonsquamous NSCLC. Elsevier 2022-08-06 /pmc/articles/PMC9667308/ /pubmed/36406000 http://dx.doi.org/10.1016/j.jtocrr.2022.100389 Text en © 2022 Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Gadgeel, Shirish
Gray, Jhanelle E.
Rizzo, Maria Teresa
Peterson, Patrick
Kim, Jong Seok
Rodríguez-Abreu, Delvys
Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189
title Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189
title_full Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189
title_fullStr Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189
title_full_unstemmed Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189
title_short Pemetrexed and Platinum Plus Pembrolizumab in Patients With Metastatic Nonsquamous NSCLC by Tumor Burden at Baseline: A Post Hoc Efficacy Analysis of KEYNOTE-189
title_sort pemetrexed and platinum plus pembrolizumab in patients with metastatic nonsquamous nsclc by tumor burden at baseline: a post hoc efficacy analysis of keynote-189
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667308/
https://www.ncbi.nlm.nih.gov/pubmed/36406000
http://dx.doi.org/10.1016/j.jtocrr.2022.100389
work_keys_str_mv AT gadgeelshirish pemetrexedandplatinumpluspembrolizumabinpatientswithmetastaticnonsquamousnsclcbytumorburdenatbaselineaposthocefficacyanalysisofkeynote189
AT grayjhanellee pemetrexedandplatinumpluspembrolizumabinpatientswithmetastaticnonsquamousnsclcbytumorburdenatbaselineaposthocefficacyanalysisofkeynote189
AT rizzomariateresa pemetrexedandplatinumpluspembrolizumabinpatientswithmetastaticnonsquamousnsclcbytumorburdenatbaselineaposthocefficacyanalysisofkeynote189
AT petersonpatrick pemetrexedandplatinumpluspembrolizumabinpatientswithmetastaticnonsquamousnsclcbytumorburdenatbaselineaposthocefficacyanalysisofkeynote189
AT kimjongseok pemetrexedandplatinumpluspembrolizumabinpatientswithmetastaticnonsquamousnsclcbytumorburdenatbaselineaposthocefficacyanalysisofkeynote189
AT rodriguezabreudelvys pemetrexedandplatinumpluspembrolizumabinpatientswithmetastaticnonsquamousnsclcbytumorburdenatbaselineaposthocefficacyanalysisofkeynote189