Unique ID issued by UMIN | UMIN000007600 |
---|---|
Receipt number | R000008968 |
Scientific Title | Phase I/II study of Chemotherapy with Nab-paclitaxel, Carboplatin and Trastuzumab in HER2-positive Locally Advanced Breast Cancer |
Date of disclosure of the study information | 2012/04/01 |
Last modified on | 2015/03/30 08:34:32 |
Phase I/II study of Chemotherapy with Nab-paclitaxel, Carboplatin and Trastuzumab in HER2-positive Locally Advanced Breast Cancer
Phase I/II study of Chemotherapy with Nab-paclitaxel, Carboplatin and Trastuzumab in HER2-positive Locally Advanced Breast Cancer
Phase I/II study of Chemotherapy with Nab-paclitaxel, Carboplatin and Trastuzumab in HER2-positive Locally Advanced Breast Cancer
Phase I/II study of Chemotherapy with Nab-paclitaxel, Carboplatin and Trastuzumab in HER2-positive Locally Advanced Breast Cancer
Japan |
Locally advanced breast cancer
Breast surgery |
Malignancy
NO
To evaluate safety and efficency in Phase I and II as combined chemotherapy of nab-paclitaxel, carboplatine, and trastzumab in HER2 positive locally advanced breast cancer
Safety,Efficacy
Phase I,II
Maximum tolerated dose and recommended dose in phase I study
Respose rate in phase II study
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
Nab-paclitaxel
20 | years-old | <= |
70 | years-old | >= |
Female
1)Patinets with a histopathological diagnosis of invasive breast cancer
2)Women for an initial diagnosis of IIIB or stage IIIC breast cancer
3)An age of 20 years to 70 years
4)Having at least one measureable lesion
5)HER2 status,IHC 3+ or FISH score>2.2, is comfirmed by biopsy specimen
6)Baseline left ventricular ejection fraction (LVEF) => 55% measured by echocardiography or MUGA scan. (comfirmed within 28 days before ragistration)
7)No clinical problem is found in ECG (comfirmed within 28 days before registraion)
8)ECOG performance status is 0 or 1
9)Adequate organ functions confirmed with following major examination
WBC=>4000mm3
Neutrophil=>2000mm3
Platelet count=>100,000/mm3
Hemoglobin=>9.0g/dL
AST,ALT=<100IU/L
Total bilirubin=<1.5mg/dL
Serum creatinine=<1.5mg/dL
Albmin=>3.0mg/dL
10)Obtained written informed consent
1)With history of hypersensitivity reaction for important medications in this treatment
2)Inflammatory breast cancer(T4d)
3)Synchronous double cancer (carcinoma in situ) which is controllable by local treatment is excluded
4)With uncontrollable infectious disease, diarrhea, ileus, diabetes, or other serious complications
5)With active pleural effusion or ascites
6)With serious heart disease, or the patient who has past history of it
7)With severe peripheral nerve disorder
8)With GI ulcer or GI hemorrhage
9)Having a past history of severe mental disorder or the patient who is under treatment of it
10)Pregnancy, or suspected pregnancy
11)HBs antigen positive or the patient for whom deoxyribonucleic acid analog is needed
12)Cases who physician judged improper to entry this trial
22
1st name | |
Middle name | |
Last name | Kenji Tezuka |
National Hospital Organization Kinki-chuo Chest Medical Center
Department of Breast Surgery
1180 Nagasonemachi Kita-ku Sakai-shi Osaka
072-252-3021
kntezuka@kch.hosp.go.jp
1st name | |
Middle name | |
Last name | Tsutomu Takashima |
Osaka Breast Cancer Chemo-Endocrine Therapy Study Group
Executive office
1-4-3 Asahimachi Abeno-ku Osaka-shi Osaka
06-6645-3838
tsutomu-@rd5.so-net.ne.jp
Department of Surgical Oncology, Osaka City University Graduate School of Medicine
None
Self funding
NO
2012 | Year | 04 | Month | 01 | Day |
Unpublished
Enrolling by invitation
2012 | Year | 02 | Month | 29 | Day |
2012 | Year | 04 | Month | 01 | Day |
2015 | Year | 09 | Month | 30 | Day |
2012 | Year | 03 | Month | 29 | Day |
2015 | Year | 03 | Month | 30 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008968