UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000027506 |
|---|---|
| Receipt number | R000031497 |
| Scientific Title | A phase II study of systemic chemotherapy with S-1 and Oxaliplatin followed by gastrectomy with D2 or D2 plus limited para-aortic lymph node dissection in HER2 negative advanced gastric or esophagogastric junction cancer with extensive lymph node metastasis |
| Date of disclosure of the study information | 2017/07/01 |
| Last modified on | 2023/09/07 16:03:00 |
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Basic information
Public title
A phase II study of systemic chemotherapy with S-1 and Oxaliplatin followed by gastrectomy with D2 or D2 plus limited para-aortic lymph node dissection in HER2 negative advanced gastric or esophagogastric junction cancer with extensive lymph node metastasis
Acronym
A phase II study of systemic chemotherapy with S-1 and Oxaliplatin followed by gastrectomy with D2 or D2 plus limited para-aortic lymph node dissection in HER2 negative advanced gastric or esophagogastric junction cancer with extensive lymph node metastasis
Scientific Title
A phase II study of systemic chemotherapy with S-1 and Oxaliplatin followed by gastrectomy with D2 or D2 plus limited para-aortic lymph node dissection in HER2 negative advanced gastric or esophagogastric junction cancer with extensive lymph node metastasis
Scientific Title:Acronym
A phase II study of systemic chemotherapy with S-1 and Oxaliplatin followed by gastrectomy with D2 or D2 plus limited para-aortic lymph node dissection in HER2 negative advanced gastric or esophagogastric junction cancer with extensive lymph node metastasis
Region
| Japan |
Condition
Condition
Gastric cancer
Classification by specialty
| Gastroenterology | Hematology and clinical oncology | Gastrointestinal surgery |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
To evaluate efficacy and safety of gastrectomy with D2 or D2 plus limited para-aortic lymph node dissection in HER2 negative advanced gastric or esophagogastric junction cancer with extensive lymph node metastasis following systemic chemotherapy with S-1 and Oxaliplatin
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Others
Trial characteristics_2
Others
Developmental phase
Phase II
Assessment
Primary outcomes
3-year overall survival
Key secondary outcomes
Proportion of R0 resection, 5-year overall survival, 3- and 5-year recurrence free survival, Proportion of completion of surgery, Proportion of completion of protocol treatment, Clinical response rate, Pathological response rate, Adverse events from chemotherapy, Operation time, Intraoperative blood loss, Surgical complications, Postoperative hospital stay
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Medicine | Maneuver |
Interventions/Control_1
Gastrectomy with D2 or D2 plus dissection of para-aortic lymph nodes diagnosed as metastases at initial diagnosis is performed after three or four 21-day cycles of S-1 plus oxaliplatin. S-1 is also given for 1 year after gastrectomy.
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 20 | years-old | <= |
Age-upper limit
| 75 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
1) Histologically proven gastric adenocarcinoma
2) HER2 negative (IHC 0 or IHC 1+, or IHC 2+/FISH -)
3) One of the following conditions is fulfilled by enhanced CT
1. Paraaortic lymph node metastasis (No.16a2/ 16b1)
2. Bulky N (at least one node of 3 cm or more in diameter, or at least three consecutive nodes each of diameter 1.5 cm or more, along the coeliac, splenic, common or proper hepatic arteries or superior mesenteric vein.)
3. Both of No.16a2/ 16b1 and bulky lymph node metastasis
4. Thoracic/ abdominal/ pelvic enhanced CT reveals none of the following findings:
i) Mediastinal lymph node metastasis
ii) Lung metastasis
iii) Peritoneal metastasis
iv) Liver metastasis
v) Pleural effusion, ascites beyond the pelvis
vi) Paraaortic No. 16a1 or No. 16b2 swelling 1cm or greater
vii) Other distant metastases (except for No. 13, No. 16a2 or No. 16b1 metastasis)
5) Neither Borrmann type 4 nor large (8cm or more) type 3
6) Length of esophageal invasion less than or equal to 3cm
7) Not stump cancer of stomach.
8) Clinically no sign of distant metastasis
9) No liver or peritoneal metastasis and CY0 by laparoscopy or laparotomy for bypass surgery within 28 days before registration
10) Age between 20 and 75 at registration
11) Performance Status (ECOG) 0 or 1
12) No prior chemotherapy, radiotherapy or endocrinotherapy
13) No prior surgery for gastric carcinoma except for bypass surgery and endoscopic mucosal resection
14) Fair oral intake with or without bypass surgery
15) Adequate organ functions defined as indicated below;
i) WBC >= 4,000/mm3 and <= 12,000/mm3
ii) Neutrophils >= 4,000/mm3
iii) Hb >= 8.0 g/dl
iv) Platelet >= 100,000/mm3
v) AST <= 100IU
vi) ALT <= 100IU
vii) T.bil <= 1.5 mg/dL
viii) Creatinine <= 1.2 mg/dL
viii) Ccr >= 60 mL/min/body
16) Written informed consent
Key exclusion criteria
1) Synchronous or metachronous (within 5 years) malignancies other than carcinoma in situ or mucosal cancer
2) Women during pregnancy or breast-feeding
3) Severe mental disease
4) Under treatment with systemic steroid
5) HBs antigen positive
6) Under treatment with flucytosine, phenytoin, or warfarin
7) Allergy to iodine
8) History of hypersensitivity to oxaliplatin or S-1
9) Peripheral motor neuropathy or peripheral sensory neuropathy by any reason
10) Edema of limbs or trunk by any reason
11) Interstitial pneumonia, pulmonary fibrosis or severe emphysema.
12) Active bacterial or fungal infection
13) Past history of myocardial infarction or unstable angina pectoris within 6 months
14) Uncontrollable hypertension
15) Uncontrollable diabetes mellitus or routine administration of insulin
Target sample size
35
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Takeshi Sano |
Organization
Cancer Institute Hospital
Division name
Division of gastroenterological surgery
Zip code
Address
3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan
TEL
03-3520-0111
takeshi.sano@jfcr.or.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Koshi Kumagai |
Organization
Cancer Institute Hospital
Division name
Division of gastroenterological surgery
Zip code
Address
3-8-31, Ariake, Koto-ku, Tokyo, 135-8550, Japan
TEL
03-3520-0111
Homepage URL
koshi.kumagai@jfcr.or.jp
Sponsor or person
Institute
Cancer Institute Hospital
Institute
Department
Personal name
Funding Source
Organization
Self-sustaining fund
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Address
Tel
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
がん研究会有明病院（東京都）
国立がん研究センター中央病院（東京都）
静岡県立静岡がんセンター（静岡県）
国立がん研究センター東病院（千葉県）
愛知県がんセンター中央病院（愛知県）
Other administrative information
Date of disclosure of the study information
| 2017 | Year | 07 | Month | 01 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Terminated
Date of protocol fixation
| 2017 | Year | 05 | Month | 25 | Day |
Date of IRB
| 2019 | Year | 02 | Month | 21 | Day |
Anticipated trial start date
| 2017 | Year | 09 | Month | 01 | Day |
Last follow-up date
| 2027 | Year | 09 | Month | 28 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2017 | Year | 05 | Month | 26 | Day |
Last modified on
| 2023 | Year | 09 | Month | 07 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031497
