Unique ID issued by UMIN | C000000170 |
---|---|
Receipt number | R000000237 |
Scientific Title | A phase II randomized study of DP(Docetaxel+Cisplatin),DJ(Docetaxel+Carboplatin),and TJ(Paclitaxel+Carboplatin) in patients with advanced and recurrent endometrial carcinoma |
Date of disclosure of the study information | 2005/09/15 |
Last modified on | 2010/12/20 11:35:55 |
A phase II randomized study of DP(Docetaxel+Cisplatin),DJ(Docetaxel+Carboplatin),and TJ(Paclitaxel+Carboplatin) in patients with advanced and recurrent endometrial carcinoma
Evaluation of Taxane and Platinum combinations in patients with advanced and recurrent endometrial carcinoma
A phase II randomized study of DP(Docetaxel+Cisplatin),DJ(Docetaxel+Carboplatin),and TJ(Paclitaxel+Carboplatin) in patients with advanced and recurrent endometrial carcinoma
Evaluation of Taxane and Platinum combinations in patients with advanced and recurrent endometrial carcinoma
Japan |
advanced or recurrent endometrial carcinoma
Obstetrics and Gynecology |
Malignancy
NO
The purpose is to assess the efficacy and safety of the treatment with Taxane plus Platinum combination chemotherapy for advanced or recurrent endometrial carcinoma. The combinations of Taxane and Platinum are as follows; Docetaxel and Cisplatin, Docetaxel and Carboplatin, AND Paclitaxel and Carboplatin.
Safety,Efficacy
Phase II
Tumor Response
Toxicity, Feasibility, Progression free survival
Interventional
Parallel
Randomized
Open -no one is blinded
Active
YES
YES
Institution is not considered as adjustment factor.
NO
Central registration
3
Treatment
Medicine |
Docetaxel 70mg/m2+CDDP 60mg/m2 day1 q 3 weeks 3courses or more
Docetaxel 60mg/m2+CBDCA AUC 6 day1 q 3 weeks 3courses or more
Paclitaxel 180mg/m2+CBDCA AUC 6 day1 q 3 weeks 3courses or more
20 | years-old | <= |
75 | years-old | > |
Female
-Histologically confirmed endometrial carcinoma
-Stage III, IV, or recurrent disease
-Measurable disease
-At least 1 uni-dimensional measurable lesion >= 20 mm by conventional CT or MR OR >= 10 mm by helical CT scan
-At least 1 target lesion
-Prior therapy:
*At least 6 months since prior cytotoxic chemotherapy
*At least 4 weeks since prior radiotherapy
*At least 2 weeks since prior oral fluorouracil, hormonal or immunologic therapy
-Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
-Adequate bone marrow, hepatic, renal, cardiac and respiratory functions
-Written informed consent
-Patients with sarcomatous element
-Active infections
-Serious complications (heart disease, interstitial lung disease, uncontrolled hypertension, diabetes mellitus and tendency to bleeding)
-Massive pleural effusion or ascites
-Neuropathy grade 2 or more; edema grade 2 or more (NCI-CTC)
-Active concomitant malignancy
-Hypersensitivity to Polysorbate 80 or Cremophor EL
-Patients judged inappropriate for this study by the physicians
90
1st name | |
Middle name | |
Last name | Daisuke Aoki, M.D. |
School of Medicine, Keio University
Department of Obstetrics and Gynecology
35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 Japan
03-3353-1211
1st name | |
Middle name | |
Last name | Daisuke Aoki, M.D. |
JGOG2041 Coordinating Office
Department of Obstetrics and Gynecology, School of Medicine, Keio University
35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 Japan
03-3353-1211
http://www.jgog.gr.jp/
Japanese Gynecologic Oncology Group
Ministry of Health, Labour and Welfare
Japanese Gynecologic Oncology Group
NO
2005 | Year | 09 | Month | 15 | Day |
Published
http://annonc.oxfordjournals.org/content/early/2010/08/07/annonc.mdq401.abstract?sid=ae1bc117-d083-4f07-a1f4-a72f54030cf8
Completed
2003 | Year | 11 | Month | 28 | Day |
2003 | Year | 12 | Month | 01 | Day |
2006 | Year | 07 | Month | 01 | Day |
2006 | Year | 09 | Month | 01 | Day |
2007 | Year | 01 | Month | 01 | Day |
2007 | Year | 04 | Month | 01 | Day |
2005 | Year | 09 | Month | 12 | Day |
2010 | Year | 12 | Month | 20 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000237