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Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review)

Because poor performance status (PS) is an independent prognostic factor in non-small cell lung cancer (NSCLC), PS scores are widely used by oncologists to make treatment decisions. Advanced NSCLC patients with an Eastern Cooperative Oncology Group PS of 2 have poor prognoses and are frequently excl...

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Autores principales: ZINNER, RALPH, GRUL, CARLA VISSEREN, SPIGEL, DAVID R., OBASAJU, COLEMAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734604/
https://www.ncbi.nlm.nih.gov/pubmed/26530033
http://dx.doi.org/10.3892/ijo.2015.3219
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author ZINNER, RALPH
GRUL, CARLA VISSEREN
SPIGEL, DAVID R.
OBASAJU, COLEMAN
author_facet ZINNER, RALPH
GRUL, CARLA VISSEREN
SPIGEL, DAVID R.
OBASAJU, COLEMAN
author_sort ZINNER, RALPH
collection PubMed
description Because poor performance status (PS) is an independent prognostic factor in non-small cell lung cancer (NSCLC), PS scores are widely used by oncologists to make treatment decisions. Advanced NSCLC patients with an Eastern Cooperative Oncology Group PS of 2 have poor prognoses and are frequently excluded from clinical trials. This article reviews the efficacy and safety of pemetrexed in this patient group. We identified English-language literature (through March 2015) involving completed and ongoing studies through searches of PubMed, meeting abstracts, ClinicalTrials.gov and the European Clinical Trials Register; search terms included ‘pemetrexed,’ ‘NSCLC’ and ‘PS2’. Only studies reporting ≥1 subset analysis of PS2 patients receiving pemetrexed were chosen. Our search identified a total of ten pemetrexed studies in PS2 patients. Eight studies included only chemonaive patients, one study included both chemonaive patients and patients with one prior chemotherapy regimen and one study included only patients with one prior regimen. In subset analyses in these studies, PS2 patients had worse outcomes than PS0-1 patients regardless of treatment. In a phase 3 study, chemonaive advanced NSCLC patients with PS2 receiving pemetrexed-carboplatin versus pemetrexed experienced improved overall survival [hazard ratio (HR)=0.62; P=0.001], progression-free survival (HR=0.46; P<0.001) and response (P=0.032). This review confirms the poorer outcomes in PS2 vs. PS0-1 patients. Although it is not an approved combination therapy, in clinical studies, PS2 patients treated with pemetrexed plus carboplatin as first-line therapy had improved response rates and survival. Additional research on PS2 patients is needed.
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spelling pubmed-47346042016-02-18 Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review) ZINNER, RALPH GRUL, CARLA VISSEREN SPIGEL, DAVID R. OBASAJU, COLEMAN Int J Oncol Articles Because poor performance status (PS) is an independent prognostic factor in non-small cell lung cancer (NSCLC), PS scores are widely used by oncologists to make treatment decisions. Advanced NSCLC patients with an Eastern Cooperative Oncology Group PS of 2 have poor prognoses and are frequently excluded from clinical trials. This article reviews the efficacy and safety of pemetrexed in this patient group. We identified English-language literature (through March 2015) involving completed and ongoing studies through searches of PubMed, meeting abstracts, ClinicalTrials.gov and the European Clinical Trials Register; search terms included ‘pemetrexed,’ ‘NSCLC’ and ‘PS2’. Only studies reporting ≥1 subset analysis of PS2 patients receiving pemetrexed were chosen. Our search identified a total of ten pemetrexed studies in PS2 patients. Eight studies included only chemonaive patients, one study included both chemonaive patients and patients with one prior chemotherapy regimen and one study included only patients with one prior regimen. In subset analyses in these studies, PS2 patients had worse outcomes than PS0-1 patients regardless of treatment. In a phase 3 study, chemonaive advanced NSCLC patients with PS2 receiving pemetrexed-carboplatin versus pemetrexed experienced improved overall survival [hazard ratio (HR)=0.62; P=0.001], progression-free survival (HR=0.46; P<0.001) and response (P=0.032). This review confirms the poorer outcomes in PS2 vs. PS0-1 patients. Although it is not an approved combination therapy, in clinical studies, PS2 patients treated with pemetrexed plus carboplatin as first-line therapy had improved response rates and survival. Additional research on PS2 patients is needed. D.A. Spandidos 2015-10-29 /pmc/articles/PMC4734604/ /pubmed/26530033 http://dx.doi.org/10.3892/ijo.2015.3219 Text en Copyright: © Zinner et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
ZINNER, RALPH
GRUL, CARLA VISSEREN
SPIGEL, DAVID R.
OBASAJU, COLEMAN
Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review)
title Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review)
title_full Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review)
title_fullStr Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review)
title_full_unstemmed Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review)
title_short Pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (Review)
title_sort pemetrexed clinical studies in performance status 2 patients with non-small cell lung cancer (review)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734604/
https://www.ncbi.nlm.nih.gov/pubmed/26530033
http://dx.doi.org/10.3892/ijo.2015.3219
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