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Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial

OBJECTIVE: Paclitaxel (P) is a standard second-line chemotherapy in the treatment of advanced gastric cancer. This study compared the clinical outcome of a paclitaxel plus raltitrexed (RP) regimen as second-line treatment in metastatic gastric cancer (MGC) patients. METHODS: An open, randomized, mul...

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Autores principales: Zhao, Xiaoying, Chen, Zhiyu, Zhang, Xiaowei, Zhu, Xiaodong, Zhang, Wen, Qiu, Lixin, Wang, Chenchen, Huang, Mingzhu, Zhang, Zhe, Li, Wenhua, Yang, Lei, Guo, Weijian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Compuscript 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546090/
https://www.ncbi.nlm.nih.gov/pubmed/37653589
http://dx.doi.org/10.20892/j.issn.2095-3941.2023.0112
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author Zhao, Xiaoying
Chen, Zhiyu
Zhang, Xiaowei
Zhu, Xiaodong
Zhang, Wen
Qiu, Lixin
Wang, Chenchen
Huang, Mingzhu
Zhang, Zhe
Li, Wenhua
Yang, Lei
Guo, Weijian
author_facet Zhao, Xiaoying
Chen, Zhiyu
Zhang, Xiaowei
Zhu, Xiaodong
Zhang, Wen
Qiu, Lixin
Wang, Chenchen
Huang, Mingzhu
Zhang, Zhe
Li, Wenhua
Yang, Lei
Guo, Weijian
author_sort Zhao, Xiaoying
collection PubMed
description OBJECTIVE: Paclitaxel (P) is a standard second-line chemotherapy in the treatment of advanced gastric cancer. This study compared the clinical outcome of a paclitaxel plus raltitrexed (RP) regimen as second-line treatment in metastatic gastric cancer (MGC) patients. METHODS: An open, randomized, multi-center phase II clinical trial was conducted involving 148 patients who were randomly assigned and treated with RP [raltitrexed (3 mg/m(2) on day 1) and paclitaxel (135 mg/m(2) on day 1 every 3 weeks)] or P [paclitaxel (135 mg/m(2) on day 1 every 3 weeks)] as 2(nd)-line chemotherapy. The primary endpoint was progression-free survival (PFS). The secondary endpoints were the overall response rate (ORR), overall survival (OS), and safety. RESULTS: PFS had a tendency to be prolonged with RP compared to P (2.7 months vs. 1.7 months; P = 0.148). OS was also prolonged with RP compared to P (10.2 months vs. 6.1 months; P = 0.140). The ORR was equal in the RP and P groups (6.8% and 4.0%; P = 0.72). The disease control rate (DCR) in the RP and P groups was 56.2% and 36.0%, respectively. Grade 3-4 treatment-related adverse events occurred in 36.2% (RP) and 28.2% (P) of patients. Frequent grade 3-4 toxicities for RP and P were neutropenia (11.0% and 4.0%), anemia (1.4% and 4.0%), and thrombocytopenia (1.4% and 5.3%), and all grades of peripheral neurotoxicity (12.3% vs. 17.3%). All grades of hepatic toxicity were demonstrated for the RP and P groups based on elevated aminotransferase levels (27.4% and 14.1%). Subgroup analysis shows if MGC was combined with ascites or peritoneal involvement, the OS of the RP regimen was longer (P = 0.05). CONCLUSIONS: Second-line palliative chemotherapy with RP was shown to prolong the PFS and OS, especially among patients with ascites or peritoneal involvement, which warrants confirmation using larger sample studies.
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spelling pubmed-105460902023-10-04 Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial Zhao, Xiaoying Chen, Zhiyu Zhang, Xiaowei Zhu, Xiaodong Zhang, Wen Qiu, Lixin Wang, Chenchen Huang, Mingzhu Zhang, Zhe Li, Wenhua Yang, Lei Guo, Weijian Cancer Biol Med Original Article OBJECTIVE: Paclitaxel (P) is a standard second-line chemotherapy in the treatment of advanced gastric cancer. This study compared the clinical outcome of a paclitaxel plus raltitrexed (RP) regimen as second-line treatment in metastatic gastric cancer (MGC) patients. METHODS: An open, randomized, multi-center phase II clinical trial was conducted involving 148 patients who were randomly assigned and treated with RP [raltitrexed (3 mg/m(2) on day 1) and paclitaxel (135 mg/m(2) on day 1 every 3 weeks)] or P [paclitaxel (135 mg/m(2) on day 1 every 3 weeks)] as 2(nd)-line chemotherapy. The primary endpoint was progression-free survival (PFS). The secondary endpoints were the overall response rate (ORR), overall survival (OS), and safety. RESULTS: PFS had a tendency to be prolonged with RP compared to P (2.7 months vs. 1.7 months; P = 0.148). OS was also prolonged with RP compared to P (10.2 months vs. 6.1 months; P = 0.140). The ORR was equal in the RP and P groups (6.8% and 4.0%; P = 0.72). The disease control rate (DCR) in the RP and P groups was 56.2% and 36.0%, respectively. Grade 3-4 treatment-related adverse events occurred in 36.2% (RP) and 28.2% (P) of patients. Frequent grade 3-4 toxicities for RP and P were neutropenia (11.0% and 4.0%), anemia (1.4% and 4.0%), and thrombocytopenia (1.4% and 5.3%), and all grades of peripheral neurotoxicity (12.3% vs. 17.3%). All grades of hepatic toxicity were demonstrated for the RP and P groups based on elevated aminotransferase levels (27.4% and 14.1%). Subgroup analysis shows if MGC was combined with ascites or peritoneal involvement, the OS of the RP regimen was longer (P = 0.05). CONCLUSIONS: Second-line palliative chemotherapy with RP was shown to prolong the PFS and OS, especially among patients with ascites or peritoneal involvement, which warrants confirmation using larger sample studies. Compuscript 2023-09-15 2023-08-31 /pmc/articles/PMC10546090/ /pubmed/37653589 http://dx.doi.org/10.20892/j.issn.2095-3941.2023.0112 Text en Copyright: © 2023, Cancer Biology & Medicine https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY) 4.0 (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Zhao, Xiaoying
Chen, Zhiyu
Zhang, Xiaowei
Zhu, Xiaodong
Zhang, Wen
Qiu, Lixin
Wang, Chenchen
Huang, Mingzhu
Zhang, Zhe
Li, Wenhua
Yang, Lei
Guo, Weijian
Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial
title Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial
title_full Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial
title_fullStr Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial
title_full_unstemmed Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial
title_short Comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: A randomized phase II clinical trial
title_sort comparing effectiveness and safety of paclitaxel plus raltitrexed vs. paclitaxel alone in second-line palliative chemotherapy for metastatic gastric adenocarcinoma: a randomized phase ii clinical trial
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546090/
https://www.ncbi.nlm.nih.gov/pubmed/37653589
http://dx.doi.org/10.20892/j.issn.2095-3941.2023.0112
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