Randomized multicenter phase III study of a modified docetaxel and cisplatin plus fluorouracil regimen compared with cisplatin and fluorouracil as first-line therapy for advanced or locally recurrent gastric cancer
Background The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a high incidence of dose-limiting toxicities. We investigated the efficacy and safety of a modified DCF (mDCF) regimen for Chinese pat...
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Published in | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association Vol. 19; no. 1; pp. 234 - 244 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Tokyo
Springer Japan
01.01.2016
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Abstract | Background
The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a high incidence of dose-limiting toxicities. We investigated the efficacy and safety of a modified DCF (mDCF) regimen for Chinese patients with advanced gastric cancer.
Methods
Untreated advanced gastric cancer patients randomly received docetaxel and cisplatin at 60 mg/m
2
(day 1) followed by fluorouracil at 600 mg/m
2
/day (days 1–5; mDCF regimen) or cisplatin at 75 mg/m
2
(day 1) followed by fluorouracil at 600 mg/m
2
/day (days 1–5; CF) every 3 weeks. The primary end point was progression-free survival (PFS). The secondary end points were OS, overall response rate (ORR), time-to-treatment failure (TTF), and safety.
Results
In total, 243 patients were randomized to treatment (mDCF regimen 121; CF 122). Compared with CF, the mDCF regimen significantly improved PFS and OS: the median PFS was 7.2 and 4.9 months, respectively [hazard ratio (HR) 0.58, log-rank
P
= 0.0008], and the median OS was 10.2 and 8.5 months, respectively (HR = 0.71,
P
= 0.0319). Additionally, the mDCF regimen improved the parameters used as secondary objectives: the ORR was 48.7 % with the mDCF regimen versus 33.9 % with CF (
P
= 0.0244); the median TTF was 3.4 months with the mDCF regimen and 2.4 months with CF (HR = 0.67,
P
= 0.0027). Grade 3 and grade 4 treatment-related adverse events occurred in 77.3 % of patients who received the mDCF regimen versus 46.1 % of patients who received CF (
P
< 0.001).
Conclusions
The mDCF regimen, compared with CF, significantly prolonged PFS and OS and enhanced ORR of Chinese patients with advanced gastric cancer. The mDCF regimen achieved efficacy comparable to that of DCF but with fewer toxicities, which is appropriate for the Chinese population. |
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AbstractList | The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a high incidence of dose-limiting toxicities. We investigated the efficacy and safety of a modified DCF (mDCF) regimen for Chinese patients with advanced gastric cancer.
Untreated advanced gastric cancer patients randomly received docetaxel and cisplatin at 60 mg/m(2) (day 1) followed by fluorouracil at 600 mg/m(2)/day (days 1-5; mDCF regimen) or cisplatin at 75 mg/m(2) (day 1) followed by fluorouracil at 600 mg/m(2)/day (days 1-5; CF) every 3 weeks. The primary end point was progression-free survival (PFS). The secondary end points were OS, overall response rate (ORR), time-to-treatment failure (TTF), and safety.
In total, 243 patients were randomized to treatment (mDCF regimen 121; CF 122). Compared with CF, the mDCF regimen significantly improved PFS and OS: the median PFS was 7.2 and 4.9 months, respectively [hazard ratio (HR) 0.58, log-rank P = 0.0008], and the median OS was 10.2 and 8.5 months, respectively (HR = 0.71, P = 0.0319). Additionally, the mDCF regimen improved the parameters used as secondary objectives: the ORR was 48.7% with the mDCF regimen versus 33.9% with CF (P = 0.0244); the median TTF was 3.4 months with the mDCF regimen and 2.4 months with CF (HR = 0.67, P = 0.0027). Grade 3 and grade 4 treatment-related adverse events occurred in 77.3 % of patients who received the mDCF regimen versus 46.1% of patients who received CF (P < 0.001).
The mDCF regimen, compared with CF, significantly prolonged PFS and OS and enhanced ORR of Chinese patients with advanced gastric cancer. The mDCF regimen achieved efficacy comparable to that of DCF but with fewer toxicities, which is appropriate for the Chinese population. The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a high incidence of dose-limiting toxicities. We investigated the efficacy and safety of a modified DCF (mDCF) regimen for Chinese patients with advanced gastric cancer.BACKGROUNDThe V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a high incidence of dose-limiting toxicities. We investigated the efficacy and safety of a modified DCF (mDCF) regimen for Chinese patients with advanced gastric cancer.Untreated advanced gastric cancer patients randomly received docetaxel and cisplatin at 60 mg/m(2) (day 1) followed by fluorouracil at 600 mg/m(2)/day (days 1-5; mDCF regimen) or cisplatin at 75 mg/m(2) (day 1) followed by fluorouracil at 600 mg/m(2)/day (days 1-5; CF) every 3 weeks. The primary end point was progression-free survival (PFS). The secondary end points were OS, overall response rate (ORR), time-to-treatment failure (TTF), and safety.METHODSUntreated advanced gastric cancer patients randomly received docetaxel and cisplatin at 60 mg/m(2) (day 1) followed by fluorouracil at 600 mg/m(2)/day (days 1-5; mDCF regimen) or cisplatin at 75 mg/m(2) (day 1) followed by fluorouracil at 600 mg/m(2)/day (days 1-5; CF) every 3 weeks. The primary end point was progression-free survival (PFS). The secondary end points were OS, overall response rate (ORR), time-to-treatment failure (TTF), and safety.In total, 243 patients were randomized to treatment (mDCF regimen 121; CF 122). Compared with CF, the mDCF regimen significantly improved PFS and OS: the median PFS was 7.2 and 4.9 months, respectively [hazard ratio (HR) 0.58, log-rank P = 0.0008], and the median OS was 10.2 and 8.5 months, respectively (HR = 0.71, P = 0.0319). Additionally, the mDCF regimen improved the parameters used as secondary objectives: the ORR was 48.7% with the mDCF regimen versus 33.9% with CF (P = 0.0244); the median TTF was 3.4 months with the mDCF regimen and 2.4 months with CF (HR = 0.67, P = 0.0027). Grade 3 and grade 4 treatment-related adverse events occurred in 77.3 % of patients who received the mDCF regimen versus 46.1% of patients who received CF (P < 0.001).RESULTSIn total, 243 patients were randomized to treatment (mDCF regimen 121; CF 122). Compared with CF, the mDCF regimen significantly improved PFS and OS: the median PFS was 7.2 and 4.9 months, respectively [hazard ratio (HR) 0.58, log-rank P = 0.0008], and the median OS was 10.2 and 8.5 months, respectively (HR = 0.71, P = 0.0319). Additionally, the mDCF regimen improved the parameters used as secondary objectives: the ORR was 48.7% with the mDCF regimen versus 33.9% with CF (P = 0.0244); the median TTF was 3.4 months with the mDCF regimen and 2.4 months with CF (HR = 0.67, P = 0.0027). Grade 3 and grade 4 treatment-related adverse events occurred in 77.3 % of patients who received the mDCF regimen versus 46.1% of patients who received CF (P < 0.001).The mDCF regimen, compared with CF, significantly prolonged PFS and OS and enhanced ORR of Chinese patients with advanced gastric cancer. The mDCF regimen achieved efficacy comparable to that of DCF but with fewer toxicities, which is appropriate for the Chinese population.CONCLUSIONSThe mDCF regimen, compared with CF, significantly prolonged PFS and OS and enhanced ORR of Chinese patients with advanced gastric cancer. The mDCF regimen achieved efficacy comparable to that of DCF but with fewer toxicities, which is appropriate for the Chinese population. Background The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a high incidence of dose-limiting toxicities. We investigated the efficacy and safety of a modified DCF (mDCF) regimen for Chinese patients with advanced gastric cancer. Methods Untreated advanced gastric cancer patients randomly received docetaxel and cisplatin at 60 mg/m 2 (day 1) followed by fluorouracil at 600 mg/m 2 /day (days 1–5; mDCF regimen) or cisplatin at 75 mg/m 2 (day 1) followed by fluorouracil at 600 mg/m 2 /day (days 1–5; CF) every 3 weeks. The primary end point was progression-free survival (PFS). The secondary end points were OS, overall response rate (ORR), time-to-treatment failure (TTF), and safety. Results In total, 243 patients were randomized to treatment (mDCF regimen 121; CF 122). Compared with CF, the mDCF regimen significantly improved PFS and OS: the median PFS was 7.2 and 4.9 months, respectively [hazard ratio (HR) 0.58, log-rank P = 0.0008], and the median OS was 10.2 and 8.5 months, respectively (HR = 0.71, P = 0.0319). Additionally, the mDCF regimen improved the parameters used as secondary objectives: the ORR was 48.7 % with the mDCF regimen versus 33.9 % with CF ( P = 0.0244); the median TTF was 3.4 months with the mDCF regimen and 2.4 months with CF (HR = 0.67, P = 0.0027). Grade 3 and grade 4 treatment-related adverse events occurred in 77.3 % of patients who received the mDCF regimen versus 46.1 % of patients who received CF ( P < 0.001). Conclusions The mDCF regimen, compared with CF, significantly prolonged PFS and OS and enhanced ORR of Chinese patients with advanced gastric cancer. The mDCF regimen achieved efficacy comparable to that of DCF but with fewer toxicities, which is appropriate for the Chinese population. Background The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a high incidence of dose-limiting toxicities. We investigated the efficacy and safety of a modified DCF (mDCF) regimen for Chinese patients with advanced gastric cancer. Methods Untreated advanced gastric cancer patients randomly received docetaxel and cisplatin at 60 mg/m^sup 2^ (day 1) followed by fluorouracil at 600 mg/m^sup 2^/day (days 1-5; mDCF regimen) or cisplatin at 75 mg/m^sup 2^ (day 1) followed by fluorouracil at 600 mg/m^sup 2^/day (days 1-5; CF) every 3 weeks. The primary end point was progression-free survival (PFS). The secondary end points were OS, overall response rate (ORR), time-to-treatment failure (TTF), and safety. Results In total, 243 patients were randomized to treatment (mDCF regimen 121; CF 122). Compared with CF, the mDCF regimen significantly improved PFS and OS: the median PFS was 7.2 and 4.9 months, respectively [hazard ratio (HR) 0.58, log-rank P = 0.0008], and the median OS was 10.2 and 8.5 months, respectively (HR = 0.71, P = 0.0319). Additionally, the mDCF regimen improved the parameters used as secondary objectives: the ORR was 48.7 % with the mDCF regimen versus 33.9 % with CF (P = 0.0244); the median TTF was 3.4 months with the mDCF regimen and 2.4 months with CF (HR = 0.67, P = 0.0027). Grade 3 and grade 4 treatment-related adverse events occurred in 77.3 % of patients who received the mDCF regimen versus 46.1 % of patients who received CF (P < 0.001). Conclusions The mDCF regimen, compared with CF, significantly prolonged PFS and OS and enhanced ORR of Chinese patients with advanced gastric cancer. The mDCF regimen achieved efficacy comparable to that of DCF but with fewer toxicities, which is appropriate for the Chinese population. |
Author | Xu, Jianming Liu, Yunpeng Shu, Yongqian Ma, Dong Bai, Yuxian Chen, Weichang Ba, Yi Dai, Guanghai Xu, Ruihua Jiao, Shunchang Shen, Lin Fan, Nanfeng Liu, Tianshu Zheng, Leizhen Wang, Jinwan Qin, Shukui Li, Jian |
Author_xml | – sequence: 1 givenname: Jinwan surname: Wang fullname: Wang, Jinwan organization: Cancer Institute and Hospital, Chinese Academy of Medical Sciences – sequence: 2 givenname: Ruihua surname: Xu fullname: Xu, Ruihua organization: Sun Yat-Sen University Cancer Center – sequence: 3 givenname: Jian surname: Li fullname: Li, Jian organization: Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute – sequence: 4 givenname: Yuxian surname: Bai fullname: Bai, Yuxian organization: Harbin Medical University Cancer Hospital – sequence: 5 givenname: Tianshu surname: Liu fullname: Liu, Tianshu organization: Fudan University Affiliated Zhong Shan Hospital – sequence: 6 givenname: Shunchang surname: Jiao fullname: Jiao, Shunchang organization: Chinese PLA General Hospital – sequence: 7 givenname: Guanghai surname: Dai fullname: Dai, Guanghai organization: Chinese PLA General Hospital – sequence: 8 givenname: Jianming surname: Xu fullname: Xu, Jianming organization: 307 Hospital of PLA – sequence: 9 givenname: Yunpeng surname: Liu fullname: Liu, Yunpeng organization: The First Hospital of China Medical University – sequence: 10 givenname: Nanfeng surname: Fan fullname: Fan, Nanfeng organization: Fujian Provincial Cancer Hospital – sequence: 11 givenname: Yongqian surname: Shu fullname: Shu, Yongqian organization: Jiangsu Provincial Hospital – sequence: 12 givenname: Yi surname: Ba fullname: Ba, Yi organization: Tianjin Medical University Cancer Institute and Hospital – sequence: 13 givenname: Dong surname: Ma fullname: Ma, Dong organization: Guangdong General Hospital – sequence: 14 givenname: Shukui surname: Qin fullname: Qin, Shukui organization: PLA Cancer Center of Bayi Hospital – sequence: 15 givenname: Leizhen surname: Zheng fullname: Zheng, Leizhen organization: Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine – sequence: 16 givenname: Weichang surname: Chen fullname: Chen, Weichang organization: Suzhou University Affiliated First Hospital – sequence: 17 givenname: Lin surname: Shen fullname: Shen, Lin email: lin100@medmail.com.cn organization: Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25604851$$D View this record in MEDLINE/PubMed |
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Copyright | The Author(s) 2015 The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2016 |
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Keywords | Safety Overall survival Advanced gastric cancer Progression-free survival Modified docetaxel and cisplatin plus fluorouracil regimen |
Language | English |
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PublicationPlace | Tokyo |
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PublicationTitle | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association |
PublicationTitleAbbrev | Gastric Cancer |
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PublicationYear | 2016 |
Publisher | Springer Japan Springer Nature B.V |
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EORTC Early Clinical Trials Group publication-title: Br J Cancer doi: 10.1038/bjc.1994.310 – volume: 24 start-page: 4991 year: 2006 end-page: 4997 ident: CR5 article-title: Phase III study of docetaxel and cisplatin plus fluorouracil compared with cisplatin and fluorouracil as first line therapy for advanced gastric cancer: a report of the V325 Study Group publication-title: J Clin Oncol doi: 10.1200/JCO.2006.06.8429 – volume: 9 start-page: 215 year: 2008 ident: 457_CR24 publication-title: Lancet Oncol doi: 10.1016/S1470-2045(08)70035-4 – volume: 124 start-page: 2997 year: 2011 ident: 457_CR13 publication-title: Chin Med J – volume: 59 start-page: 233 year: 2012 ident: 457_CR14 publication-title: Neoplasma doi: 10.4149/neo_2012_030 – volume: 102 start-page: 475 year: 2010 ident: 457_CR17 publication-title: Br J Cancer doi: 10.1038/sj.bjc.6605522 – volume: 50 start-page: 157 year: 2007 ident: 457_CR16 publication-title: Korean J Gastroenterol – volume: 25 start-page: 3205 year: 2007 ident: 457_CR8 publication-title: J Clin Oncol doi: 10.1200/JCO.2006.10.4968 – volume: 70 start-page: 380 year: 1994 ident: 457_CR22 publication-title: Br J Cancer doi: 10.1038/bjc.1994.310 – volume: 8 start-page: e60320 year: 2013 ident: 457_CR7 publication-title: PLoS One doi: 10.1371/journal.pone.0060320 – volume: 10 start-page: 1063 year: 2009 ident: 457_CR26 publication-title: Lancet Oncol doi: 10.1016/S1470-2045(09)70259-1 – volume: 127 start-page: 2893 year: 2010 ident: 457_CR2 publication-title: Int J Cancer doi: 10.1002/ijc.25516 – volume: 77 start-page: 1166 year: 2006 ident: 457_CR27 publication-title: Chirurg doi: 10.1007/s00104-006-1249-5 – volume: 27 start-page: 680 year: 2010 ident: 457_CR15 publication-title: Med Oncol doi: 10.1007/s12032-009-9268-y – volume: 92 start-page: 205 year: 2000 ident: 457_CR20 publication-title: J Natl Cancer Inst doi: 10.1093/jnci/92.3.205 – volume: 140 start-page: 319 year: 2014 ident: 457_CR25 publication-title: J Cancer Res Clin Oncol doi: 10.1007/s00432-013-1563-5 – volume: 116 start-page: 1446 year: 2010 ident: 457_CR18 publication-title: Cancer (Phila) doi: 10.1002/cncr.24925 – volume: 15 start-page: 403 year: 2013 ident: 457_CR19 publication-title: Clin Transl Oncol doi: 10.1007/s12094-012-0942-8 – volume: 23 start-page: 313 year: 2012 ident: 457_CR10 publication-title: Anticancer Drugs doi: 10.1097/CAD.0b013e32834fd780 – volume: 13 start-page: 87 year: 1996 ident: 457_CR23 publication-title: Med Oncol doi: 10.1007/BF02993858 – volume: 72 start-page: 37 year: 1993 ident: 457_CR3 publication-title: Cancer doi: 10.1002/1097-0142(19930701)72:1<37::AID-CNCR2820720109>3.0.CO;2-P – volume: 60 start-page: 1449 year: 2011 ident: 457_CR6 publication-title: Gut doi: 10.1136/gut.2010.228254 – ident: 457_CR21 – ident: 457_CR28 – volume: 96 start-page: 48 year: 2010 ident: 457_CR9 publication-title: Tumori doi: 10.1177/030089161009600108 – volume: 28 start-page: 433 year: 2005 ident: 457_CR12 publication-title: Am J Clin Oncol doi: 10.1097/01.coc.0000162424.69631.79 – volume: 14 start-page: e535 year: 2013 ident: 457_CR1 publication-title: Lancet Oncol doi: 10.1016/S1470-2045(13)70436-4 – volume: 18 start-page: 1673 year: 2007 ident: 457_CR11 publication-title: Ann Oncol doi: 10.1093/annonc/mdm269 – volume: 71 start-page: 587 year: 1995 ident: 457_CR4 publication-title: Br J Cancer doi: 10.1038/bjc.1995.114 – volume: 24 start-page: 4991 year: 2006 ident: 457_CR5 publication-title: J Clin Oncol doi: 10.1200/JCO.2006.06.8429 – reference: 17091285 - Chirurg. 2006 Dec;77(12):1166-7 – reference: 22040543 - Chin Med J (Engl). 2011 Oct;124(19):2997-3002 – reference: 17075117 - J Clin Oncol. 2006 Nov 1;24(31):4991-7 – reference: 8508427 - Cancer. 1993 Jul 1;72(1):37-41 – reference: 20108336 - Cancer. 2010 Mar 15;116(6):1446-53 – reference: 24176572 - Lancet Oncol. 2013 Nov;14(12):e535-47 – reference: 22248282 - Neoplasma. 2012;59(2):233-6 – reference: 24366758 - J Cancer Res Clin Oncol. 2014 Feb;140(2):319-28 – reference: 19818685 - Lancet Oncol. 2009 Nov;10(11):1063-9 – reference: 17660494 - Ann Oncol. 2007 Oct;18(10):1673-9 – reference: 18282805 - Lancet Oncol. 2008 Mar;9(3):215-21 – reference: 17885280 - Korean J Gastroenterol. 2007 Sep;50(3):157-63; discussion 207-9 – reference: 7914428 - Br J Cancer. 1994 Aug;70(2):380-3 – reference: 7533517 - Br J Cancer. 1995 Mar;71(3):587-91 – reference: 21705456 - Gut. 2011 Nov;60(11):1449-72 – reference: 19633962 - Med Oncol. 2010 Sep;27(3):680-4 – reference: 20068567 - Br J Cancer. 2010 Feb 2;102(3):475-81 – reference: 22241172 - Anticancer Drugs. 2012 Mar;23(3):313-20 – reference: 23593191 - PLoS One. 2013;8(4):e60320 – reference: 23054756 - Clin Transl Oncol. 2013 May;15(5):403-8 – reference: 10655437 - J Natl Cancer Inst. 2000 Feb 2;92(3):205-16 – reference: 17664467 - J Clin Oncol. 2007 Aug 1;25(22):3205-9 – reference: 9013471 - Med Oncol. 1996 Jun;13(2):87-93 – reference: 21351269 - Int J Cancer. 2010 Dec 15;127(12):2893-917 – reference: 20437857 - Tumori. 2010 Jan-Feb;96(1):48-53 – reference: 16199979 - Am J Clin Oncol. 2005 Oct;28(5):433-8 |
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The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer,... The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer, but with a... Background The V325 study showed that docetaxel, cisplatin, and fluorouracil (DCF) prolonged overall survival (OS) of patients with advanced gastric cancer,... |
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SubjectTerms | Abdominal Surgery Adult Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Cancer Research Cisplatin - administration & dosage Cisplatin - adverse effects Female Fluorouracil - administration & dosage Fluorouracil - adverse effects Gastric cancer Gastroenterology Humans Male Medicine Medicine & Public Health Middle Aged Neoplasm Recurrence, Local Oncology Original Original Article Stomach Neoplasms - drug therapy Stomach Neoplasms - mortality Stomach Neoplasms - pathology Surgical Oncology Survival Rate Taxoids - administration & dosage Taxoids - adverse effects Treatment Outcome Young Adult |
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Title | Randomized multicenter phase III study of a modified docetaxel and cisplatin plus fluorouracil regimen compared with cisplatin and fluorouracil as first-line therapy for advanced or locally recurrent gastric cancer |
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