| Unique ID issued by UMIN | UMIN000000806 |
|---|---|
| Receipt number | R000000966 |
| Scientific Title | Multicenter phase II trial to Prevent Docetaxel-Induced Nail change using a Frozen Glove with docetaxel (T) and cyclophosphamide(C) as adjuvant chemotherapy for patients with high risk, node negative, early stage breast cancer: Tokai Breast Cancer Clinical Research Group (TBCRG) 03 trial |
| Date of disclosure of the study information | 2007/09/01 |
| Last modified on | 2009/09/23 11:35:57 |
Multicenter phase II trial to Prevent Docetaxel-Induced Nail change using a Frozen Glove with docetaxel (T) and cyclophosphamide(C) as adjuvant chemotherapy for patients with high risk, node negative, early stage breast cancer: Tokai Breast Cancer Clinical Research Group (TBCRG) 03 trial
TBCRG03
Multicenter phase II trial to Prevent Docetaxel-Induced Nail change using a Frozen Glove with docetaxel (T) and cyclophosphamide(C) as adjuvant chemotherapy for patients with high risk, node negative, early stage breast cancer: Tokai Breast Cancer Clinical Research Group (TBCRG) 03 trial
TBCRG03
| Japan |
Breast cancer
| Breast surgery |
Malignancy
NO
Prevention of nail change by frozen glove
Safety,Efficacy
Exploratory
Explanatory
Phase II
Prevention of nail change by frozen glove
Safety, feasibility
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
| Medicine | Device,equipment |
Frozen glove to prevent docetaxel-induced nail toxicities with right hand.
Docetaxel 75 mg/m2 IV Day 1Cyclophosphamide 600 mg/m2 IV Day 1 Every 21 days X 4 CyclesUse standard premedication
| 20 | years-old | <= |
| 70 | years-old | >= |
Female
1.Patients with early stage breast cancer (M0)
2.High risk node negative patients
3.Age >20 years and < 70 years,
4.ECOG performance status 0-1
5.No more than 12 weeks after most recent surgery
6.Sufficient organ function
7.Signed informed consent
8.No heart disease
1.As neoadjuvant and adjuvant therapy , treated hormone therapy and chemotherapy
2.HER2 / neu gene overexpressed or amplified
3.A history of whitlow and cold allergy
4.Bilateral breast cancer and Inflammatory breast cancer
5.Uncontrolled medical conditions
6.Hepatitis B
7.A history of other malignancies within the last 5 years except for adequately treated non-melanoma skin cancer or carcinoma in situ of the cervix
8.Sever infection
9.Peripheral neuropathy
10.Pleural or pericardial effusion requiring treatment
11.Pregnant or lactating women and women of child bearing potential not using contraception.
12.Grade2-4 Severe peripheral edema.
13.Significant interstitial pneumonia or pulmonary fibrosis by CT scan or X-ray
14.A history of hypersensitivity reaction to drugs formulated with Polysorbate 80
15.Severe psychiatric disorders
16.Patients judged by the investigator to be unfit to be enrolled into the study
50
| 1st name | |
| Middle name | |
| Last name | Hiroji Iwata |
Aichi Cancer Center Hospital
Breast Oncology
1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan
052-762-6111
| 1st name | |
| Middle name | |
| Last name |
Data Center Oncology Unit of Japan Clinical Research Support Unit (J-CRSU)
Data Center of Comprehensive Support Project for Oncology Research of Breast Cancer (CSPOR-BC)
Nishiyama-kogyo Ochanomizu building 5F, 1-2-13, Yushima, Bunkyo-ku, Tokyo, 113-0034, Japan
03-3254-8029
http://www.csp.or.jp/
support@csp.or.jp
Tokai Breast Cancer Clinical Research Group (TBCRG)
Public Health Research Foundation
Non profit foundation
Japan
NO
| 2007 | Year | 09 | Month | 01 | Day |
Unpublished
Completed
| 2007 | Year | 05 | Month | 13 | Day |
| 2007 | Year | 07 | Month | 01 | Day |
| 2008 | Year | 12 | Month | 01 | Day |
| 2009 | Year | 09 | Month | 01 | Day |
| 2009 | Year | 09 | Month | 01 | Day |
| 2009 | Year | 12 | Month | 01 | Day |
| 2007 | Year | 08 | Month | 23 | Day |
| 2009 | Year | 09 | Month | 23 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000966