Cargando…
A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China
Oxaliplatin plus S-1 (SOX) was a first-line regimen for advanced gastric cancer. The continuous administration of S-1 for 3 weeks can result in unacceptable gastrointestinal and hematological toxicities. Therefore, an alternative regimen (administration of S-1 for 1-week followed by 1-week rest) is...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531169/ https://www.ncbi.nlm.nih.gov/pubmed/31096513 http://dx.doi.org/10.1097/MD.0000000000015696 |
_version_ | 1783420774121472000 |
---|---|
author | Xiao, Cheng Qian, Jiong Zheng, Yulong Song, Fang Wang, Qiangfeng Jiang, Haiping Mao, Chenyu Xu, Nong |
author_facet | Xiao, Cheng Qian, Jiong Zheng, Yulong Song, Fang Wang, Qiangfeng Jiang, Haiping Mao, Chenyu Xu, Nong |
author_sort | Xiao, Cheng |
collection | PubMed |
description | Oxaliplatin plus S-1 (SOX) was a first-line regimen for advanced gastric cancer. The continuous administration of S-1 for 3 weeks can result in unacceptable gastrointestinal and hematological toxicities. Therefore, an alternative regimen (administration of S-1 for 1-week followed by 1-week rest) is warrant for improved tolerability and noninferiority efficacy. We conducted a study to evaluate the efficacy and safety of biweekly SOX as the first-line chemotherapy in patients with metastatic or advanced gastric cancer in China. Patients with metastatic or previously untreated advanced gastric cancer were enrolled. Oxaliplatin was administered intravenously at a dose of 85 mg/m(2) on day 1, while S-1 was administered orally in doses of 80, 100, or 120 mg/day depending on different body surface areas of <1.25 m(2), 1.25–1.5 m(2), or >1.5 m(2) respectively; the total dose of S-1 was administered twice daily on days 1–7 followed by a 7-day rest. This schedule was repeated every 2 weeks until disease progressed or intolerable toxicity occurred. Forty-six patients (M/F = 33/13) received biweekly oxaliplatin and S-1 as first-line chemotherapy. A total of 257 treatment cycles were administered and the median number of cycles administered was 6. Thirty-six patients (78.3%) received second-line chemotherapy. The median progression free survival and median overall survival was 4.4 months (95% CI, 3.37–5.36 months) and 10.3 months (95% CI, 8.88–11.3 months), respectively. The 1-year and 2-year survival rate was 41% and 13%. The objective response rate was 30.43%, and the disease control rate was 76.08%. The observed adverse events of Grade 3/4 included were leukocytopenia (13.04%); anemia (13.04%); neutropenia (15.22%); neurological toxicity (2.17%); diarrhea (2.17%). The biweekly SOX regimen as first-line treatment was active and well tolerated in Chinese patients with metastatic or advanced gastric cancer. |
format | Online Article Text |
id | pubmed-6531169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-65311692019-06-25 A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China Xiao, Cheng Qian, Jiong Zheng, Yulong Song, Fang Wang, Qiangfeng Jiang, Haiping Mao, Chenyu Xu, Nong Medicine (Baltimore) Research Article Oxaliplatin plus S-1 (SOX) was a first-line regimen for advanced gastric cancer. The continuous administration of S-1 for 3 weeks can result in unacceptable gastrointestinal and hematological toxicities. Therefore, an alternative regimen (administration of S-1 for 1-week followed by 1-week rest) is warrant for improved tolerability and noninferiority efficacy. We conducted a study to evaluate the efficacy and safety of biweekly SOX as the first-line chemotherapy in patients with metastatic or advanced gastric cancer in China. Patients with metastatic or previously untreated advanced gastric cancer were enrolled. Oxaliplatin was administered intravenously at a dose of 85 mg/m(2) on day 1, while S-1 was administered orally in doses of 80, 100, or 120 mg/day depending on different body surface areas of <1.25 m(2), 1.25–1.5 m(2), or >1.5 m(2) respectively; the total dose of S-1 was administered twice daily on days 1–7 followed by a 7-day rest. This schedule was repeated every 2 weeks until disease progressed or intolerable toxicity occurred. Forty-six patients (M/F = 33/13) received biweekly oxaliplatin and S-1 as first-line chemotherapy. A total of 257 treatment cycles were administered and the median number of cycles administered was 6. Thirty-six patients (78.3%) received second-line chemotherapy. The median progression free survival and median overall survival was 4.4 months (95% CI, 3.37–5.36 months) and 10.3 months (95% CI, 8.88–11.3 months), respectively. The 1-year and 2-year survival rate was 41% and 13%. The objective response rate was 30.43%, and the disease control rate was 76.08%. The observed adverse events of Grade 3/4 included were leukocytopenia (13.04%); anemia (13.04%); neutropenia (15.22%); neurological toxicity (2.17%); diarrhea (2.17%). The biweekly SOX regimen as first-line treatment was active and well tolerated in Chinese patients with metastatic or advanced gastric cancer. Wolters Kluwer Health 2019-05-17 /pmc/articles/PMC6531169/ /pubmed/31096513 http://dx.doi.org/10.1097/MD.0000000000015696 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Research Article Xiao, Cheng Qian, Jiong Zheng, Yulong Song, Fang Wang, Qiangfeng Jiang, Haiping Mao, Chenyu Xu, Nong A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China |
title | A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China |
title_full | A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China |
title_fullStr | A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China |
title_full_unstemmed | A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China |
title_short | A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China |
title_sort | phase ii study of biweekly oxaliplatin plus s-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in china |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531169/ https://www.ncbi.nlm.nih.gov/pubmed/31096513 http://dx.doi.org/10.1097/MD.0000000000015696 |
work_keys_str_mv | AT xiaocheng aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT qianjiong aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT zhengyulong aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT songfang aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT wangqiangfeng aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT jianghaiping aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT maochenyu aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT xunong aphaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT xiaocheng phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT qianjiong phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT zhengyulong phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT songfang phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT wangqiangfeng phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT jianghaiping phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT maochenyu phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina AT xunong phaseiistudyofbiweeklyoxaliplatinpluss1combinationchemotherapyasafirstlinetreatmentforpatientswithmetastaticoradvancedgastriccancerinchina |