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Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity

OBJECTIVES: Nivolumab is used at 3 mg/kg or fixed doses of 240 mg every 2 weeks. There was no dose–response/toxicity relationship of nivolumab. This study evaluated the efficacy of low-dose nivolumab as an alternative to the financial toxicity of standard-dose nivolumab in treatment of non-small cel...

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Autores principales: Yoo, Shin Hye, Keam, Bhumsuk, Kim, Miso, Kim, Se Hyun, Kim, Yu Jung, Kim, Tae Min, Kim, Dong-Wan, Lee, Jong Seok, Heo, Dae Seog
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069908/
https://www.ncbi.nlm.nih.gov/pubmed/30094065
http://dx.doi.org/10.1136/esmoopen-2018-000332
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author Yoo, Shin Hye
Keam, Bhumsuk
Kim, Miso
Kim, Se Hyun
Kim, Yu Jung
Kim, Tae Min
Kim, Dong-Wan
Lee, Jong Seok
Heo, Dae Seog
author_facet Yoo, Shin Hye
Keam, Bhumsuk
Kim, Miso
Kim, Se Hyun
Kim, Yu Jung
Kim, Tae Min
Kim, Dong-Wan
Lee, Jong Seok
Heo, Dae Seog
author_sort Yoo, Shin Hye
collection PubMed
description OBJECTIVES: Nivolumab is used at 3 mg/kg or fixed doses of 240 mg every 2 weeks. There was no dose–response/toxicity relationship of nivolumab. This study evaluated the efficacy of low-dose nivolumab as an alternative to the financial toxicity of standard-dose nivolumab in treatment of non-small cell lung cancer (NSCLC). METHODS: Outcomes of patients with NSCLC treated with nivolumab as a routine practice at two tertiary hospitals in Korea were retrospectively analysed. Patients who could not afford standard nivolumab treatment received low-dose nivolumab (20 or 100 mg fixed dose every 3 weeks). Others received standard dose of 3 mg/kg every 2 weeks. Progression-free survival (PFS) and overall survival (OS) were measured and compared between low-dose and standard-dose groups in overall and stratified analyses according to programmed death-ligand 1 (PD-L1) status. RESULTS: Among the 47 patients with NSCLC, 18 received low-dose nivolumab. PD-L1 positivity was observed in 13 (27.7%) patients and did not differ between the groups. During 5.2 months of follow-up, the objective response rate was 13.8% in the standard-dose group and 16.7% in the low-dose group (p=0.788). Dosing of nivolumab or PD-L1 expression did not significantly affect PFS or OS. CONCLUSION: Low-dose nivolumab can be effective in NSCLC and is worth considering as an alternative option to reducing financial toxicity. The efficacy of low-dose nivolumab requires study.
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spelling pubmed-60699082018-08-09 Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity Yoo, Shin Hye Keam, Bhumsuk Kim, Miso Kim, Se Hyun Kim, Yu Jung Kim, Tae Min Kim, Dong-Wan Lee, Jong Seok Heo, Dae Seog ESMO Open Original Research OBJECTIVES: Nivolumab is used at 3 mg/kg or fixed doses of 240 mg every 2 weeks. There was no dose–response/toxicity relationship of nivolumab. This study evaluated the efficacy of low-dose nivolumab as an alternative to the financial toxicity of standard-dose nivolumab in treatment of non-small cell lung cancer (NSCLC). METHODS: Outcomes of patients with NSCLC treated with nivolumab as a routine practice at two tertiary hospitals in Korea were retrospectively analysed. Patients who could not afford standard nivolumab treatment received low-dose nivolumab (20 or 100 mg fixed dose every 3 weeks). Others received standard dose of 3 mg/kg every 2 weeks. Progression-free survival (PFS) and overall survival (OS) were measured and compared between low-dose and standard-dose groups in overall and stratified analyses according to programmed death-ligand 1 (PD-L1) status. RESULTS: Among the 47 patients with NSCLC, 18 received low-dose nivolumab. PD-L1 positivity was observed in 13 (27.7%) patients and did not differ between the groups. During 5.2 months of follow-up, the objective response rate was 13.8% in the standard-dose group and 16.7% in the low-dose group (p=0.788). Dosing of nivolumab or PD-L1 expression did not significantly affect PFS or OS. CONCLUSION: Low-dose nivolumab can be effective in NSCLC and is worth considering as an alternative option to reducing financial toxicity. The efficacy of low-dose nivolumab requires study. BMJ Publishing Group 2018-07-25 /pmc/articles/PMC6069908/ /pubmed/30094065 http://dx.doi.org/10.1136/esmoopen-2018-000332 Text en © European Society for Medical Oncology (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Original Research
Yoo, Shin Hye
Keam, Bhumsuk
Kim, Miso
Kim, Se Hyun
Kim, Yu Jung
Kim, Tae Min
Kim, Dong-Wan
Lee, Jong Seok
Heo, Dae Seog
Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity
title Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity
title_full Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity
title_fullStr Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity
title_full_unstemmed Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity
title_short Low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity
title_sort low-dose nivolumab can be effective in non-small cell lung cancer: alternative option for financial toxicity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069908/
https://www.ncbi.nlm.nih.gov/pubmed/30094065
http://dx.doi.org/10.1136/esmoopen-2018-000332
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