Cargando…

Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials

BACKGROUND: There are two main choices of administration route of recombinant human endostatin (Endostar) available and the treatment options of concurrent chemoradiotherapy (CCRT) have changed over time. The aim of this study was to observe the long‐term efficacy and safety of different administrat...

Descripción completa

Detalles Bibliográficos
Autores principales: Honglian, Ma, Zhouguang, Hui, Fang, PENG, Lujun, Zhao, Dongming, Li, Yujin, Xu, Yong, Bao, Liming, Xu, Yirui, Zhai, Xiao, Hu, Jin, Wang, Yue, Kong, Lvhua, Wang, Ming, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113061/
https://www.ncbi.nlm.nih.gov/pubmed/32068962
http://dx.doi.org/10.1111/1759-7714.13333
_version_ 1783513596113715200
author Honglian, Ma
Zhouguang, Hui
Fang, PENG
Lujun, Zhao
Dongming, Li
Yujin, Xu
Yong, Bao
Liming, Xu
Yirui, Zhai
Xiao, Hu
Jin, Wang
Yue, Kong
Lvhua, Wang
Ming, Chen
author_facet Honglian, Ma
Zhouguang, Hui
Fang, PENG
Lujun, Zhao
Dongming, Li
Yujin, Xu
Yong, Bao
Liming, Xu
Yirui, Zhai
Xiao, Hu
Jin, Wang
Yue, Kong
Lvhua, Wang
Ming, Chen
author_sort Honglian, Ma
collection PubMed
description BACKGROUND: There are two main choices of administration route of recombinant human endostatin (Endostar) available and the treatment options of concurrent chemoradiotherapy (CCRT) have changed over time. The aim of this study was to observe the long‐term efficacy and safety of different administration routes of Endostar combined with CCRT. METHODS: Patients with unresectable stage III non‐small cell lung cancer (NSCLC) from two phase II trials were included as two cohorts. Both were treated with Endostar combined with CCRT. Endostar was administrated by intravenous injection (7.5 mg/m(2)/day, seven days) in the IV arm and by continuous intravenous pumping (7.5 mg/m(2)/24 hours, 120 hours) in the CIV arm. RESULTS: A total of 48 patients were included in the IV arm and 67 patients in the CIV arm. The median progression‐free survival (PFS), overall survival (OS), local recurrence‐free survival (LRFS) and distant metastasis‐free survival (DMFS) in the IV arm and CIV arm were 9.9 months versus 15.4 months (HR = 0.751, 95% CI 0.487–1.160, P = 0.200), 24.0 months versus 38.5 months (HR = 0.746, 95% CI 0.473–1.178, P = 0.209), 32.3 months versus 27.1 months (HR = 1.193, 95% CI 0.673–2.115, P = 0.546), 20.1 months versus 49.7 months (HR = 0.603, 95% CI 0.351–1.036, P = 0.067). The one, three, five‐year PFS in the IV arm and CIV arm was 45.8% versus 52.9%, 18.3% versus 31.4%, and 18.3% versus 27.7% and the one, three, five‐year OS was 81.2% versus 82.1%, 31.1% versus 50.3%, and 31.1% versus 41%, respectively. Incidence of hematological adverse reactions were numerically lower in the CIV arm than the IV arm. CONCLUSIONS: Endostar delivered by CIV with CCRT may be a better option than IV in terms of potential survival and safety for unresectable stage III NSCLC. KEY POINTS: Significant findings of the study Endostar delivered by continuous intravenous pumping might achieve more favorable survival over intravenous injection and reduce adverse hematological reactions in patients with unresectable stage III NSCLC treated with Endostar combined with CCRT.What this study adds The administration route of recombinant human endostatin is also one key factor for survival and safety to consider when treating patients with unresectable stage III NSCLC.
format Online
Article
Text
id pubmed-7113061
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley & Sons Australia, Ltd
record_format MEDLINE/PubMed
spelling pubmed-71130612020-04-02 Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials Honglian, Ma Zhouguang, Hui Fang, PENG Lujun, Zhao Dongming, Li Yujin, Xu Yong, Bao Liming, Xu Yirui, Zhai Xiao, Hu Jin, Wang Yue, Kong Lvhua, Wang Ming, Chen Thorac Cancer Original Articles BACKGROUND: There are two main choices of administration route of recombinant human endostatin (Endostar) available and the treatment options of concurrent chemoradiotherapy (CCRT) have changed over time. The aim of this study was to observe the long‐term efficacy and safety of different administration routes of Endostar combined with CCRT. METHODS: Patients with unresectable stage III non‐small cell lung cancer (NSCLC) from two phase II trials were included as two cohorts. Both were treated with Endostar combined with CCRT. Endostar was administrated by intravenous injection (7.5 mg/m(2)/day, seven days) in the IV arm and by continuous intravenous pumping (7.5 mg/m(2)/24 hours, 120 hours) in the CIV arm. RESULTS: A total of 48 patients were included in the IV arm and 67 patients in the CIV arm. The median progression‐free survival (PFS), overall survival (OS), local recurrence‐free survival (LRFS) and distant metastasis‐free survival (DMFS) in the IV arm and CIV arm were 9.9 months versus 15.4 months (HR = 0.751, 95% CI 0.487–1.160, P = 0.200), 24.0 months versus 38.5 months (HR = 0.746, 95% CI 0.473–1.178, P = 0.209), 32.3 months versus 27.1 months (HR = 1.193, 95% CI 0.673–2.115, P = 0.546), 20.1 months versus 49.7 months (HR = 0.603, 95% CI 0.351–1.036, P = 0.067). The one, three, five‐year PFS in the IV arm and CIV arm was 45.8% versus 52.9%, 18.3% versus 31.4%, and 18.3% versus 27.7% and the one, three, five‐year OS was 81.2% versus 82.1%, 31.1% versus 50.3%, and 31.1% versus 41%, respectively. Incidence of hematological adverse reactions were numerically lower in the CIV arm than the IV arm. CONCLUSIONS: Endostar delivered by CIV with CCRT may be a better option than IV in terms of potential survival and safety for unresectable stage III NSCLC. KEY POINTS: Significant findings of the study Endostar delivered by continuous intravenous pumping might achieve more favorable survival over intravenous injection and reduce adverse hematological reactions in patients with unresectable stage III NSCLC treated with Endostar combined with CCRT.What this study adds The administration route of recombinant human endostatin is also one key factor for survival and safety to consider when treating patients with unresectable stage III NSCLC. John Wiley & Sons Australia, Ltd 2020-02-18 2020-04 /pmc/articles/PMC7113061/ /pubmed/32068962 http://dx.doi.org/10.1111/1759-7714.13333 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, 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 Original Articles
Honglian, Ma
Zhouguang, Hui
Fang, PENG
Lujun, Zhao
Dongming, Li
Yujin, Xu
Yong, Bao
Liming, Xu
Yirui, Zhai
Xiao, Hu
Jin, Wang
Yue, Kong
Lvhua, Wang
Ming, Chen
Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials
title Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials
title_full Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials
title_fullStr Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials
title_full_unstemmed Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials
title_short Different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage III non‐small cell lung cancer: Updated follow‐up results from two phase II trials
title_sort different administration routes of recombinant human endostatin combined with concurrent chemoradiotherapy might lead to different efficacy and safety profile in unresectable stage iii non‐small cell lung cancer: updated follow‐up results from two phase ii trials
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113061/
https://www.ncbi.nlm.nih.gov/pubmed/32068962
http://dx.doi.org/10.1111/1759-7714.13333
work_keys_str_mv AT honglianma differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT zhouguanghui differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT fangpeng differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT lujunzhao differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT dongmingli differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT yujinxu differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT yongbao differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT limingxu differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT yiruizhai differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT xiaohu differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT jinwang differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT yuekong differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT lvhuawang differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials
AT mingchen differentadministrationroutesofrecombinanthumanendostatincombinedwithconcurrentchemoradiotherapymightleadtodifferentefficacyandsafetyprofileinunresectablestageiiinonsmallcelllungcancerupdatedfollowupresultsfromtwophaseiitrials