Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort Study

Hieu Trong Nguyen,1 Kien Hung Do,2 Nguyen Ba Le,3 Thang Tran4 1Department of Medical Oncology 2, Hanoi Oncology Hospital, Hanoi, Vietnam; 2Department of Medical Oncology 1, National Cancer Hospital of Vietnam, Hanoi, Vietnam; 3Ha Thanh Hospital, Hanoi, Vietnam; 4Department of Medical Oncology 4, Nat...

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Main Authors: Nguyen HT, Do KH, Le NB, Tran T
Format: Article
Language:English
Published: Dove Medical Press 2022-09-01
Series:Cancer Management and Research
Subjects:
Online Access:https://www.dovepress.com/treatment-outcome-and-safety-of-the-tcx-regimen-for-advanced-gastric-c-peer-reviewed-fulltext-article-CMAR
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author Nguyen HT
Do KH
Le NB
Tran T
author_facet Nguyen HT
Do KH
Le NB
Tran T
author_sort Nguyen HT
collection DOAJ
description Hieu Trong Nguyen,1 Kien Hung Do,2 Nguyen Ba Le,3 Thang Tran4 1Department of Medical Oncology 2, Hanoi Oncology Hospital, Hanoi, Vietnam; 2Department of Medical Oncology 1, National Cancer Hospital of Vietnam, Hanoi, Vietnam; 3Ha Thanh Hospital, Hanoi, Vietnam; 4Department of Medical Oncology 4, National Cancer Hospital of Vietnam, Hanoi, VietnamCorrespondence: Hieu Trong Nguyen, Department of Medical Oncology 2, Hanoi Oncology Hospital, 42A Thanh Nhan, Thanh Nhan, Hai Ba Trung, Hanoi, Vietnam, Tel +84 983230112, Email hieunt@bvubhn.vnObjective: To evaluate the outcome and safety of the paclitaxel, carboplatin, and capecitabine (TCX) regimen in patients with advanced gastric cancer.Methods: Advanced gastric cancer patients received the TCX regimen for up to six cycles, which were 3 weeks apart. Paclitaxel (175 mg/m2) was given over a 3-hour infusion, followed by carboplatin in a 1-hour infusion on day 1. Capecitabine (850 mg/m2) was given orally twice daily from day 1 to day 14. Primary endpoints were progression-free survival (PFS) and overall survival (OS).Results: Among 83 patients at stage IVa and IVb, the median PFS was 9.3 months; 6-month, 1-year, and 2-year PFS were 74.6%, 32.5%, and 14.4%, respectively. The median OS was 17.0 months; 6-month, 1-year, and 2-year OS were 97.5%, 68.7%, and 21.7%, respectively. In the multivariable Cox regression model, higher CEA was associated with poor OS. Common adverse events included hand-food syndrome (77.9%), peripheral neuropathy (63.2%), fatigue (68.7%), and nausea (54.2%).Conclusion: The TCX regimen provided good survival and a better safety profile. More clinical trials are needed to confirm its treatment efficacy and safety, especially in comparison with other triplet regimens.Keywords: paclitaxel, carboplatin, capecitabine, advanced gastric cancer, efficacy
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spelling doaj.art-8053a4d557c84e909df8baf8234267552022-12-22T03:13:47ZengDove Medical PressCancer Management and Research1179-13222022-09-01Volume 142825283778363Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort StudyNguyen HTDo KHLe NBTran THieu Trong Nguyen,1 Kien Hung Do,2 Nguyen Ba Le,3 Thang Tran4 1Department of Medical Oncology 2, Hanoi Oncology Hospital, Hanoi, Vietnam; 2Department of Medical Oncology 1, National Cancer Hospital of Vietnam, Hanoi, Vietnam; 3Ha Thanh Hospital, Hanoi, Vietnam; 4Department of Medical Oncology 4, National Cancer Hospital of Vietnam, Hanoi, VietnamCorrespondence: Hieu Trong Nguyen, Department of Medical Oncology 2, Hanoi Oncology Hospital, 42A Thanh Nhan, Thanh Nhan, Hai Ba Trung, Hanoi, Vietnam, Tel +84 983230112, Email hieunt@bvubhn.vnObjective: To evaluate the outcome and safety of the paclitaxel, carboplatin, and capecitabine (TCX) regimen in patients with advanced gastric cancer.Methods: Advanced gastric cancer patients received the TCX regimen for up to six cycles, which were 3 weeks apart. Paclitaxel (175 mg/m2) was given over a 3-hour infusion, followed by carboplatin in a 1-hour infusion on day 1. Capecitabine (850 mg/m2) was given orally twice daily from day 1 to day 14. Primary endpoints were progression-free survival (PFS) and overall survival (OS).Results: Among 83 patients at stage IVa and IVb, the median PFS was 9.3 months; 6-month, 1-year, and 2-year PFS were 74.6%, 32.5%, and 14.4%, respectively. The median OS was 17.0 months; 6-month, 1-year, and 2-year OS were 97.5%, 68.7%, and 21.7%, respectively. In the multivariable Cox regression model, higher CEA was associated with poor OS. Common adverse events included hand-food syndrome (77.9%), peripheral neuropathy (63.2%), fatigue (68.7%), and nausea (54.2%).Conclusion: The TCX regimen provided good survival and a better safety profile. More clinical trials are needed to confirm its treatment efficacy and safety, especially in comparison with other triplet regimens.Keywords: paclitaxel, carboplatin, capecitabine, advanced gastric cancer, efficacyhttps://www.dovepress.com/treatment-outcome-and-safety-of-the-tcx-regimen-for-advanced-gastric-c-peer-reviewed-fulltext-article-CMARpaclitaxelcarboplatincapecitabineadvanced gastric cancerefficacy
spellingShingle Nguyen HT
Do KH
Le NB
Tran T
Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort Study
Cancer Management and Research
paclitaxel
carboplatin
capecitabine
advanced gastric cancer
efficacy
title Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort Study
title_full Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort Study
title_fullStr Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort Study
title_full_unstemmed Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort Study
title_short Treatment Outcome and Safety of the TCX Regimen for Advanced Gastric Cancer: A Prospective Cohort Study
title_sort treatment outcome and safety of the tcx regimen for advanced gastric cancer a prospective cohort study
topic paclitaxel
carboplatin
capecitabine
advanced gastric cancer
efficacy
url https://www.dovepress.com/treatment-outcome-and-safety-of-the-tcx-regimen-for-advanced-gastric-c-peer-reviewed-fulltext-article-CMAR
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