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Status unknownNCT00587145Updated Jan 7, 2008

Phase II Study of Perioperative S-1 Plus Docetaxel in Patients With Localized Advanced Gastric Cancer

A Phase 2 interventional study of S-1,Docetaxel in Stomach Neoplasms, sponsored by National Cancer Center, Korea. Status unknown at 1 site in Korea, Republic of. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2008-01-07.

Sponsored by National Cancer Center, Korea · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2007), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
44
Allocation
Non-randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

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
02

Conditions studied

  • Stomach Neoplasms

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Keywords

  • Stomach Neoplasms
  • Secondary
  • Combination chemotherapy
  • S-1
  • Docetaxel
  • oxaliplatin
03

In context

Stomach Neoplasms

2,851 studies on the registry are indexed under Stomach Neoplasms; 863 are open to participants now.

This study's planned enrollment of 44 is below the median of 67 across 2,095 interventional studies indexed under Stomach Neoplasms.

Browse Stomach Neoplasms studies →

Lead sponsor

National Cancer Center, Korea is the lead sponsor of 193 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. 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
  2. No distant metastatic disease in laparoscopy
  3. Age: 18-70 years
  4. Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  5. 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
  6. 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
  7. Patients should sign a written informed consent before study entry

Exclusion criteria

Exclusion Criteria:

  1. CT Stage I, II, M1 or N3, which is metastatic node in WHO TNM classification, according to Japanese TNM classification system
  2. Prior chemotherapy or radiotherapy
  3. 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
  4. Serious concurrent infection or nonmalignant illness that is uncontrolled or whose control may be jeopardized by complications of study therapy
  5. Other malignancy within the past 3 years except non-melanomatous skin cancer or carcinoma in situ of the cervix
  6. Psychiatric disorder that would preclude compliance
  7. Pregnant, nursing women or patients with reproductive potential without contraception
  8. Patients receiving a concomitant treatment with drugs interacting with S-1 such as flucytosine, phenytoin, or warfarin et al.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
44 participants (estimated)

Interventions

  • DrugS-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

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What researchers measure

Primary outcomes

  1. To evaluate the clinical responses to preoperative S-1 plus docetaxel

    Time frame: During chemotherapy

Secondary outcomes

  1. 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

07

Study locations

1 of 1 sites recruiting
  • National Cancer Center Korea
    Goyang,, Gyeonggi, Korea, Republic of
    • Sook Ryun Park, M.D · Contact · sukryun73@ncc.re.kr · +82-31-920-1609
    • So Yun Park, MS · Contact · tomongmong@naver.com · +82-31-920-2307
    • 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 · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 7, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00587145
Lead sponsor
National Cancer Center, Korea
First posted
Jan 7, 2008
Start date
May 2006
Primary completion
Mar 2009 (estimated)
Completion
May 2009 (estimated)
Last update
Jan 7, 2008

Study contacts

Sook Ryun Park, M.D
Contact
sukryun73@ncc.re.kr
+82-31-920-1609
So Yun Park, MS
Contact
tomongmong@naver.com
+82-31-920-2307
Sook Ryun Park, M.D
principal investigator · National Cancer Center, Korea

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2007. You cannot join it, but the record below documents what was studied.

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