Unique ID issued by UMIN | UMIN000006742 |
---|---|
Receipt number | R000007966 |
Scientific Title | Efficacy and Safety study of adjuvant therapy with capecitabine plus oxaliplatin (XELOX) for the Japanese patient with Stage III curative resection Colon cancer -Phase II study |
Date of disclosure of the study information | 2011/11/20 |
Last modified on | 2021/05/25 15:54:57 |
Efficacy and Safety study of adjuvant therapy with capecitabine plus oxaliplatin (XELOX) for the Japanese patient with Stage III curative resection Colon cancer -Phase II study
Efficacy and Safety study of adjuvant therapy with XELOX for the Japanese patient with StageIII curative resection Colon cancer
Efficacy and Safety study of adjuvant therapy with capecitabine plus oxaliplatin (XELOX) for the Japanese patient with Stage III curative resection Colon cancer -Phase II study
Efficacy and Safety study of adjuvant therapy with XELOX for the Japanese patient with StageIII curative resection Colon cancer
Japan |
Colon cancer
Gastroenterology | Hematology and clinical oncology | Gastrointestinal surgery |
Malignancy
NO
Efficacy and Safety study of adjuvant therapy with capecitabine plus oxaliplatin (XELOX) for the Japanese patient with Stage III curative resection Colon cancer
Safety,Efficacy
Phase II
3 year disease free survival
Completion rate of treatment,Safety, Duration of administration of oxaliplatin, Incidence of Peripheral neuropathy and hand foot syndrome, Incidence and Survival of hand foot syndrome, dose intensity,Efficacy of Stage IIIa, IIIb
Interventional
Single arm
Non-randomized
Open -no one is blinded
Historical
1
Treatment
Medicine |
Adjuvant chemotherapy with capecitabine plus oxaliplatin
20 | years-old | <= |
Not applicable |
Male and Female
1) Histologically proved colon cancer(adenocarcinoma)
2) Stage III colon cancer or RS
3) >=D2 lymph node dissection
4) Pathological curability is A
5) >=20years-old
6) ECOG performance status 0-1
7) No prior chemotherapy or radiotherapy
8) Enough oral food intake possible
9) Adequate organ function
10) Able to start within 8 weeks after surgery
11) Written informed consent
1) Present with diarrhea
2) synchronous or metachronous (within 5 years) malignancy other than carcinoma in situ
3) CTCAE v4.0>Grade1 of peripheral neuropathy
4) regular use of insulin
5) uncontrollable congestive heart failure, angina,hypertension, arrhythmia
6) Severe mental disease
7) active infection
8) Pregnant or breast-feeding women
9) Woman might be pregnant
10) Inadequate physical condition, as diagnosed by primary physician
140
1st name | katsuki |
Middle name | |
Last name | Danno |
Minoh City Hospital
Department of Surgery
562-0014
5-7-1 Kayano, Minoh, Osaka 562-0014, Japan
072-728-2001
k.danno@minoh-hp.jp
1st name | Mamoru |
Middle name | |
Last name | Uemura |
Osaka University Graduate School of Medicine
Department of Surgery
565-0871
2-2 Yamadaoka, Suita, Osaka 565-0871,Japan
06-6879-3251
muemura@gesurg.med.osaka-u.ac.jp
Multicenter Study Group of Osaka (MCSGO), Colorectal Cancer Treatment Group
None
Self funding
The ethics committee of Osaka University
2-15 Yamadaoka Suita-city Osaka,Japan
06-6879-5685
rinri@hp-crc.med.osaka-u.ac.jp
NO
2011 | Year | 11 | Month | 20 | Day |
Unpublished
195
No longer recruiting
2011 | Year | 11 | Month | 09 | Day |
2011 | Year | 11 | Month | 09 | Day |
2011 | Year | 11 | Month | 10 | Day |
2024 | Year | 03 | Month | 31 | Day |
2011 | Year | 11 | Month | 17 | Day |
2021 | Year | 05 | Month | 25 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007966