Cargando…

Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study)

BACKGROUND: This study aimed to investigate the superiority of nab-paclitaxel plus S-1 (AS) over oxaliplatin plus S-1 (SOX) in patients with advanced gastric cancer (AGC). METHODS: In this multicenter, randomized, phase III superiority trial, eligible patients with unresectable, locally advanced gas...

Descripción completa

Detalles Bibliográficos
Autores principales: Dai, Yu-Hong, Yu, Xiong-Jie, Xu, Hui-Ting, Zhuang, Liang, Zhang, Ming-Sheng, Zou, Yan-Mei, Fu, Qiang, Qiu, Hong, Yuan, Xiang-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379568/
https://www.ncbi.nlm.nih.gov/pubmed/35983025
http://dx.doi.org/10.1177/17588359221118020
_version_ 1784768701127458816
author Dai, Yu-Hong
Yu, Xiong-Jie
Xu, Hui-Ting
Zhuang, Liang
Zhang, Ming-Sheng
Zou, Yan-Mei
Fu, Qiang
Qiu, Hong
Yuan, Xiang-Lin
author_facet Dai, Yu-Hong
Yu, Xiong-Jie
Xu, Hui-Ting
Zhuang, Liang
Zhang, Ming-Sheng
Zou, Yan-Mei
Fu, Qiang
Qiu, Hong
Yuan, Xiang-Lin
author_sort Dai, Yu-Hong
collection PubMed
description BACKGROUND: This study aimed to investigate the superiority of nab-paclitaxel plus S-1 (AS) over oxaliplatin plus S-1 (SOX) in patients with advanced gastric cancer (AGC). METHODS: In this multicenter, randomized, phase III superiority trial, eligible patients with unresectable, locally advanced gastric adenocarcinoma were recruited and randomly assigned (1:1) to receive AS (nab-paclitaxel 260 mg/m(2) on day 1 or 130 mg/m(2) on days 1 and 8; oral S-1 40–60 mg twice daily for 14 days) or SOX (130 mg/m(2) oxaliplatin on day 1; oral S-1 40–60 mg twice daily for 14 days) every 3 weeks for up to six cycles. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were overall survival, objective response rate, and safety. RESULTS: Owing to slow enrolment, an unplanned interim analysis was performed, resulting in the early termination of the study on 31 December 2021 (data cutoff). Between March 2019 and March 2021, 97 patients (AS, n = 48; SOX, n = 49) were treated and evaluated for efficacy and safety of AS and SOX. As of the data cutoff, the median follow-up was 23.13 months [95% confidence interval (CI), 13.39–32.87]. The median PFS was 9.03 months (95% CI, 6.50–11.56) in the AS group and 5.07 months (95% CI, 4.33–5.81) in the SOX group, demonstrating a better PFS tendency following AS treatment than SOX treatment (hazard ratio = 0.59; 95% CI, 0.37–0.94; p = 0.03). The most common grade 3 or worse adverse events were anemia, neutropenia, and leukopenia in both groups, with a higher incidence of thrombocytopenia in the SOX group. CONCLUSION: Although this study was terminated early, the results demonstrated a better PFS tendency in patients with AGC who were treated with AS than in those treated with SOX, with controllable toxicities. TRIAL REGISTRATION: Clinical Trials.gov identifiers: NCT03801668. Registered January 11, 2019.
format Online
Article
Text
id pubmed-9379568
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-93795682022-08-17 Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study) Dai, Yu-Hong Yu, Xiong-Jie Xu, Hui-Ting Zhuang, Liang Zhang, Ming-Sheng Zou, Yan-Mei Fu, Qiang Qiu, Hong Yuan, Xiang-Lin Ther Adv Med Oncol Original Research BACKGROUND: This study aimed to investigate the superiority of nab-paclitaxel plus S-1 (AS) over oxaliplatin plus S-1 (SOX) in patients with advanced gastric cancer (AGC). METHODS: In this multicenter, randomized, phase III superiority trial, eligible patients with unresectable, locally advanced gastric adenocarcinoma were recruited and randomly assigned (1:1) to receive AS (nab-paclitaxel 260 mg/m(2) on day 1 or 130 mg/m(2) on days 1 and 8; oral S-1 40–60 mg twice daily for 14 days) or SOX (130 mg/m(2) oxaliplatin on day 1; oral S-1 40–60 mg twice daily for 14 days) every 3 weeks for up to six cycles. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were overall survival, objective response rate, and safety. RESULTS: Owing to slow enrolment, an unplanned interim analysis was performed, resulting in the early termination of the study on 31 December 2021 (data cutoff). Between March 2019 and March 2021, 97 patients (AS, n = 48; SOX, n = 49) were treated and evaluated for efficacy and safety of AS and SOX. As of the data cutoff, the median follow-up was 23.13 months [95% confidence interval (CI), 13.39–32.87]. The median PFS was 9.03 months (95% CI, 6.50–11.56) in the AS group and 5.07 months (95% CI, 4.33–5.81) in the SOX group, demonstrating a better PFS tendency following AS treatment than SOX treatment (hazard ratio = 0.59; 95% CI, 0.37–0.94; p = 0.03). The most common grade 3 or worse adverse events were anemia, neutropenia, and leukopenia in both groups, with a higher incidence of thrombocytopenia in the SOX group. CONCLUSION: Although this study was terminated early, the results demonstrated a better PFS tendency in patients with AGC who were treated with AS than in those treated with SOX, with controllable toxicities. TRIAL REGISTRATION: Clinical Trials.gov identifiers: NCT03801668. Registered January 11, 2019. SAGE Publications 2022-08-12 /pmc/articles/PMC9379568/ /pubmed/35983025 http://dx.doi.org/10.1177/17588359221118020 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Dai, Yu-Hong
Yu, Xiong-Jie
Xu, Hui-Ting
Zhuang, Liang
Zhang, Ming-Sheng
Zou, Yan-Mei
Fu, Qiang
Qiu, Hong
Yuan, Xiang-Lin
Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study)
title Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study)
title_full Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study)
title_fullStr Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study)
title_full_unstemmed Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study)
title_short Nab-paclitaxel plus S-1 versus oxaliplatin plus S-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase III trial (GAPSO study)
title_sort nab-paclitaxel plus s-1 versus oxaliplatin plus s-1 as first-line treatment in advanced gastric cancer: results of a multicenter, randomized, phase iii trial (gapso study)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379568/
https://www.ncbi.nlm.nih.gov/pubmed/35983025
http://dx.doi.org/10.1177/17588359221118020
work_keys_str_mv AT daiyuhong nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT yuxiongjie nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT xuhuiting nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT zhuangliang nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT zhangmingsheng nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT zouyanmei nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT fuqiang nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT qiuhong nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy
AT yuanxianglin nabpaclitaxelpluss1versusoxaliplatinpluss1asfirstlinetreatmentinadvancedgastriccancerresultsofamulticenterrandomizedphaseiiitrialgapsostudy