Unique ID issued by UMIN | UMIN000002064 |
---|---|
Receipt number | R000002516 |
Scientific Title | A phaseI/II study of TS-1 and Docetaxel with Metastatic Breast Cancer patients resisting for Docetaxel |
Date of disclosure of the study information | 2009/06/11 |
Last modified on | 2011/12/10 09:12:09 |
A phaseI/II study of TS-1 and Docetaxel with Metastatic Breast Cancer patients resisting for Docetaxel
A phaseI/II study of TS-1 and Docetaxel with Metastatic Breast Cancer patients resisting for Docetaxel (TABRET)
A phaseI/II study of TS-1 and Docetaxel with Metastatic Breast Cancer patients resisting for Docetaxel
A phaseI/II study of TS-1 and Docetaxel with Metastatic Breast Cancer patients resisting for Docetaxel (TABRET)
Japan |
Breast Cancer
Breast surgery |
Malignancy
NO
To evaluate the clinical effectiveness of TS-1 + Taxotere compared to Docetaxel alone with Taxotere resisting metastatic Breast Cancer.
Safety,Efficacy
Confirmatory
Pragmatic
Phase I,II
Phase I: Decide most tolerable dose and
recommend dose of medicine
Phase II: Response rate
Phase I: Adverse events
Phase II: Disease free survival time, all survival time and adverse
events
Interventional
Factorial
Non-randomized
Open -no one is blinded
Uncontrolled
2
Treatment
Medicine |
Phase I
TS-1 is administered orally on days
1-14 and stop on days 15-28.
This schedule is one course.
Taxotere is injected by vein on day1
and 15. The dose level is below.
Level 0 30mg/m2
Level 1 40mg/m2
Level 2 50mg/m2
Level 3 60mg/m2
3-6 patients will be enrolled at
each level
Phase II
Recommended dose of TS-1/Taxotere is used with 25 breast cancer patients
involving who recommended level patients in phase I.
20 | years-old | <= |
75 | years-old | >= |
Female
1) Histologically confirmed breast cancer patients
2) Brest cancer patients not performed curative resection
3) Breast cancer patients receiving with TXT therapy and are diagnosed as SD by diagnostic image
4) More than 20 years old and less 75 years old
5) Performance status(ECOG) shows from 0 to one
6) Expected survival time more than
3 months at least
7) Measurable region can be diagnosed
by RECIST
8) Not received by 5-FU derivatives
9) Adequate organ functions
10) Written informed consent
1) Concomitant malignancy
2) Patient with contraindicate TS-1 and TXT
3) Complications including severe heart disease
4) Patient with cardiac infarction within 6 months
5) Serious renal function disturbance
6) Patient with cirrhosis
7) Patient with dyspnea by pheumonitis and lung fibrosis
8) Patient with uncontrolled diabetia
9) Patient with infectious
10)Gravida and having will of pregnancy
11) Patient with chemical allergy
12) Unsuitable patients by doctors diagnosis
25
1st name | |
Middle name | |
Last name | Katsuhiro Tanaka |
Kawasaki Medical School
Breast and Thyroid Surgery
577,Matsushima, Kurashiki, Okayama 701-0192, Japan
086-462-1111
1st name | |
Middle name | |
Last name | Katsuhiro Tanaka |
Kawasaki Medical School
Breast and Thyroid Surgery
577,Matsushima, Kurashiki, Okayama 701-0192, Japan
086-462-1111
tanakaka@med.kawasaki-m.ac.jp
Department of Breast and Thyroid Surgery, Kawasaki Medical School
Kawasaki Medical School
Self funding
None
NO
2009 | Year | 06 | Month | 11 | Day |
Unpublished
no registry
Terminated
2008 | Year | 10 | Month | 29 | Day |
2009 | Year | 08 | Month | 01 | Day |
2011 | Year | 12 | Month | 01 | Day |
2011 | Year | 12 | Month | 01 | Day |
2011 | Year | 12 | Month | 01 | Day |
2011 | Year | 12 | Month | 01 | Day |
2009 | Year | 06 | Month | 10 | Day |
2011 | Year | 12 | Month | 10 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000002516