Cargando…

SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation

OBJECTIVE: This study aimed to verify the survival superiority of the combination of intraperitoneal perfusion and systemic chemotherapy over standard systemic chemotherapy. METHODS: A total of 78 advanced gastric cancer patients with malignant ascites were randomly divided into D-SOX group (intrape...

Descripción completa

Detalles Bibliográficos
Autores principales: Bin, Yehong, Lan, Dong, Bao, Wenguang, Yang, Haiyan, Zhou, Shengsheng, Huang, Fengxiang, Wang, Man, Peng, Zhigang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917651/
https://www.ncbi.nlm.nih.gov/pubmed/35279214
http://dx.doi.org/10.1186/s13063-022-06143-w
_version_ 1784668594786795520
author Bin, Yehong
Lan, Dong
Bao, Wenguang
Yang, Haiyan
Zhou, Shengsheng
Huang, Fengxiang
Wang, Man
Peng, Zhigang
author_facet Bin, Yehong
Lan, Dong
Bao, Wenguang
Yang, Haiyan
Zhou, Shengsheng
Huang, Fengxiang
Wang, Man
Peng, Zhigang
author_sort Bin, Yehong
collection PubMed
description OBJECTIVE: This study aimed to verify the survival superiority of the combination of intraperitoneal perfusion and systemic chemotherapy over standard systemic chemotherapy. METHODS: A total of 78 advanced gastric cancer patients with malignant ascites were randomly divided into D-SOX group (intraperitoneal infusion of docetaxel 30 mg/m(2) on d1 and d8, intravenous oxaliplatin 100 mg/m(2) on d1, and oral administration of S-1 on d1-d14) and DOS group (intravenous docetaxel 60 mg/m(2) on d1, intravenous oxaliplatin 100 mg/m(2) on d1, and oral administration of S-1 on d1-d14). Efficacy of both groups was evaluated every 2 cycles with 21 days as a cycle. The primary endpoint was overall survival, and the secondary endpoints were objective response rate, ascites control rate, negative conversion rate of ascites cytology, and side effects. RESULTS: The median overall survival in D-SOX group was significantly higher than that in the DOS group (11.7 vs 10.3 months, HR 0.52, 95%CI 0.31–0.86, P = 0.005). The ascites control rate in the D-SOX group was 58.9% and 30.8% in DOS group (95%CI 42.8–75.1% vs 95%CI 15.6–45.9%, P = 0.012). Besides, the adverse reactions were tolerable in both groups, and patients in the D-SOX group had lower grade 3/4 blood toxicity than that in the DOS group (26% vs 54%, P = 0.01). CONCLUSION: Compared with traditional systemic chemotherapy, docetaxel intraperitoneal infusion combined with chemotherapy has better therapeutic effect on gastric cancer ascites, with better survival benefit and tolerance and less hematological toxicity, which is worthy of further research and clinical application.
format Online
Article
Text
id pubmed-8917651
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-89176512022-03-21 SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation Bin, Yehong Lan, Dong Bao, Wenguang Yang, Haiyan Zhou, Shengsheng Huang, Fengxiang Wang, Man Peng, Zhigang Trials Research OBJECTIVE: This study aimed to verify the survival superiority of the combination of intraperitoneal perfusion and systemic chemotherapy over standard systemic chemotherapy. METHODS: A total of 78 advanced gastric cancer patients with malignant ascites were randomly divided into D-SOX group (intraperitoneal infusion of docetaxel 30 mg/m(2) on d1 and d8, intravenous oxaliplatin 100 mg/m(2) on d1, and oral administration of S-1 on d1-d14) and DOS group (intravenous docetaxel 60 mg/m(2) on d1, intravenous oxaliplatin 100 mg/m(2) on d1, and oral administration of S-1 on d1-d14). Efficacy of both groups was evaluated every 2 cycles with 21 days as a cycle. The primary endpoint was overall survival, and the secondary endpoints were objective response rate, ascites control rate, negative conversion rate of ascites cytology, and side effects. RESULTS: The median overall survival in D-SOX group was significantly higher than that in the DOS group (11.7 vs 10.3 months, HR 0.52, 95%CI 0.31–0.86, P = 0.005). The ascites control rate in the D-SOX group was 58.9% and 30.8% in DOS group (95%CI 42.8–75.1% vs 95%CI 15.6–45.9%, P = 0.012). Besides, the adverse reactions were tolerable in both groups, and patients in the D-SOX group had lower grade 3/4 blood toxicity than that in the DOS group (26% vs 54%, P = 0.01). CONCLUSION: Compared with traditional systemic chemotherapy, docetaxel intraperitoneal infusion combined with chemotherapy has better therapeutic effect on gastric cancer ascites, with better survival benefit and tolerance and less hematological toxicity, which is worthy of further research and clinical application. BioMed Central 2022-03-12 /pmc/articles/PMC8917651/ /pubmed/35279214 http://dx.doi.org/10.1186/s13063-022-06143-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Bin, Yehong
Lan, Dong
Bao, Wenguang
Yang, Haiyan
Zhou, Shengsheng
Huang, Fengxiang
Wang, Man
Peng, Zhigang
SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation
title SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation
title_full SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation
title_fullStr SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation
title_full_unstemmed SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation
title_short SOX combined with intraperitoneal perfusion of docetaxel compared with DOS regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation
title_sort sox combined with intraperitoneal perfusion of docetaxel compared with dos regimen in the first-line therapy for advanced gastric cancer with malignant ascites: a prospective observation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917651/
https://www.ncbi.nlm.nih.gov/pubmed/35279214
http://dx.doi.org/10.1186/s13063-022-06143-w
work_keys_str_mv AT binyehong soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation
AT landong soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation
AT baowenguang soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation
AT yanghaiyan soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation
AT zhoushengsheng soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation
AT huangfengxiang soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation
AT wangman soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation
AT pengzhigang soxcombinedwithintraperitonealperfusionofdocetaxelcomparedwithdosregimeninthefirstlinetherapyforadvancedgastriccancerwithmalignantascitesaprospectiveobservation