Phase II Study of Perioperative S-1 Plus Docetaxel in Patients With Localized Advanced Gastric Cancer
The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2007 by National Cancer Center, Korea.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
National Cancer Center, Korea
Information provided by:
National Cancer Center, Korea
ClinicalTrials.gov Identifier:
NCT00587145
First received: December 21, 2007
Last updated: NA
Last verified: December 2007
History: No changes posted
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
This study is an open-label, single center, and a single arm phase II study to evaluate the clinical response and safety of perioperative S-1 plus docetaxel. Perioperative chemotherapy is composed of 3 cycles of preoperative S-1/docetaxel and 3 cycles of postoperative S-1/docetaxel.Chemotherapy regimen:
- S-1 80 mg/m2/day every 12-h p.o. on days 1(evening)-15 (morning)
- Docetaxel 35 mg/m2 mixed in d5w 250 ml iv over 60-min on days 1 and 8
| Condition | Intervention | Phase |
|---|---|---|
|
Stomach Neoplasms |
Drug: S-1,Docetaxel |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase II Study of Perioperative S-1 Plus Docetaxel in Patients With Localized Advanced Gastric Cancer |
Resource links provided by NLM:
Further study details as provided by National Cancer Center, Korea:
Primary Outcome Measures:
- To evaluate the clinical responses to preoperative S-1 plus docetaxel [ Time Frame: During chemotherapy ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- the clinical downstaging,the pathologic responses, toxicity profile,the disease-free survival,overall survival,the effect of CYP2A6 genetic polymorphisms on the pharmacokinetics and the difference in pharmacokinetics between before and after gastrectomy [ Time Frame: During study period ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 44 |
| Study Start Date: | May 2006 |
| Estimated Study Completion Date: | May 2009 |
| Estimated Primary Completion Date: | March 2009 (Final data collection date for primary outcome measure) |
Intervention Details:
-
Drug: S-1,Docetaxel
- S-1 80 mg/m2/day every 12-h p.o. on days 1(evening)-15 (morning)
- Docetaxel 35 mg/m2 mixed in d5w 250 ml iv over 60-min on days 1 and 8
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Histologically or cytologically confirmed localized gastric adenocarcinoma as defined by CT stage III and IV (M0) (but not N3, which is metastatic node in WHO TNM classification), according to Japanese TNM classification system
- No distant metastatic disease in laparoscopy
- Age: 18-70 years
- Eastern Cooperative Oncology Group (ECOG) performance status 0-1
- Disease status must be that of measurable disease as defined by RECIST: Measurable lesions: lesions that can be accurately measured in at least one dimension by abdominal CT, if the longest diameter to be recorded is at least 10 mm with spiral CT
- Adequate major organ function including the following: Hematopoietic function: WBC ³ 4,000/mm3, ANC ³ 1,500/mm3, Platelet ³ 100,000/mm3Hepatic function: serum bilirubin £ 1.5 mg/dl, AST/ALT levels £ 2.5 x UNLRenal function: serum creatinine £ 1.5 mg/dl
- Patients should sign a written informed consent before study entry
Exclusion Criteria:
- CT Stage I, II, M1 or N3, which is metastatic node in WHO TNM classification, according to Japanese TNM classification system
- Prior chemotherapy or radiotherapy
- Inadequate cardiovascular function:New York Heart Association class III or IV heart diseaseUnstable angina or myocardial infarction within the past 6 monthsHistory of significant ventricular arrhythmia requiring medication with antiarrhythmics or significant conduction system abnormality
- Serious concurrent infection or nonmalignant illness that is uncontrolled or whose control may be jeopardized by complications of study therapy
- Other malignancy within the past 3 years except non-melanomatous skin cancer or carcinoma in situ of the cervix
- Psychiatric disorder that would preclude compliance
- Pregnant, nursing women or patients with reproductive potential without contraception
- Patients receiving a concomitant treatment with drugs interacting with S-1 such as flucytosine, phenytoin, or warfarin et al.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00587145
Contacts
| Contact: Sook Ryun Park, M.D | +82-31-920-1609 | sukryun73@ncc.re.kr |
| Contact: So Yun Park, MS | +82-31-920-2307 | tomongmong@naver.com |
Locations
| Korea, Republic of | |
| National Cancer Center Korea | Recruiting |
| Goyang,, Gyeonggi, Korea, Republic of | |
| Contact: Sook Ryun Park, M.D +82-31-920-1609 sukryun73@ncc.re.kr | |
| Contact: So Yun Park, MS +82-31-920-2307 tomongmong@naver.com | |
| Sub-Investigator: Noe Kyeong Kim, M.D | |
| Sub-Investigator: Young Iee Park Park, M.D.Ph.D | |
| Sub-Investigator: Young Woo Kim,, M.D | |
| Sub-Investigator: Keun Won Ryu, M.D | |
| Sub-Investigator: Jun Ho Lee, M.D | |
| Sub-Investigator: Il Ju Choi, M.D | |
| Sub-Investigator: Chan Gyoo Kim, M.D | |
| Sub-Investigator: Jong-Yeul Lee, M.D | |
| Sub-Investigator: Jong Seok Lee, M.D | |
| Sub-Investigator: Myeong-Cherl Kook Kook, M.D | |
| Sub-Investigator: Hyeong-Seok Lim, M.D | |
Sponsors and Collaborators
National Cancer Center, Korea
Investigators
| Principal Investigator: | Sook Ryun Park, M.D | National Cancer Center, Korea |
More Information
No publications provided
| Responsible Party: | Sook Ryun Park, M.D., National Cancer Center, Korea |
| ClinicalTrials.gov Identifier: | NCT00587145 History of Changes |
| Other Study ID Numbers: | NCCCTS-06-190, 82-31-920-1609 |
| Study First Received: | December 21, 2007 |
| Last Updated: | December 21, 2007 |
| Health Authority: | Korea: Food and Drug Administration |
Keywords provided by National Cancer Center, Korea:
|
Stomach Neoplasms Secondary Combination chemotherapy |
S-1 Docetaxel oxaliplatin |
Additional relevant MeSH terms:
|
Stomach Neoplasms Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Neoplasms by Site Digestive System Diseases |
Gastrointestinal Diseases Stomach Diseases Docetaxel Antineoplastic Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 16, 2013