Unique ID issued by UMIN | UMIN000005130 |
---|---|
Receipt number | R000006101 |
Scientific Title | Dasatinib discontinuation for Chronic Myelogenous Leukemia-Chronic Phase with One Year Complete Molecular Remission. |
Date of disclosure of the study information | 2011/03/01 |
Last modified on | 2012/09/05 17:15:59 |
Dasatinib discontinuation for Chronic
Myelogenous Leukemia-Chronic Phase with One Year Complete Molecular Remission.
Dasatinib discontinuation for Chronic
Myelogenous Leukemia-Chronic Phase with One Year Complete Molecular Remission.
(DADI trial)
Dasatinib discontinuation for Chronic
Myelogenous Leukemia-Chronic Phase with One Year Complete Molecular Remission.
Dasatinib discontinuation for Chronic
Myelogenous Leukemia-Chronic Phase with One Year Complete Molecular Remission.
(DADI trial)
Japan |
chronic myeloid leukemia
Hematology and clinical oncology |
Malignancy
YES
The purpose of this study is molecular relapse free survival rate after discontinuation of dasatinib in patients with Chronic Myelogenous Leukemia-Chronic Phase who have maintained complete molecular remission for at least 1 year.
Efficacy
Exploratory
Explanatory
Phase II
Molecular relapse free survival rate after discontinuation of dasatinib at 6 months.
1)Molecular relapse free survival rate after discontinuation of dasatinib at 12 months.
2)Evaluate potential prognostic factors for molecular relapse free survival.
i)We assessed LGL expansions,
ii)dose of dasatinib and time to CMR,
iii)total dose of dasatinib in last 12 months during CMR,
iv)methods and response of previous therapy,
v)previous interferon therapy,
vi)sex
vii) sokal risk group
3)Molecular remission rate after dasatinib re-challenge in cases of molecular relapse.
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
Discontinuation of dasatinib in patients with Chronic Myelogenous Leukemia-Chronic Phase who have maintained complete molecular remission for at least 1 year.
15 | years-old | <= |
Not applicable |
Male and Female
1. Patients with Chronic Myelogenous Leukemia-Chronic Phase who have maintained complete molecular remission for at least 1 year.
2. ECOG performance status (PS) score 0-2
3. Adequate organ function (hepatic, renal and lung)
4. Signed written informed consent
1. Concurrent malignancy other than CML
2.Women who are pregnant or breastfeeding
3. A serious uncontrolled medical disorder that would impair the ability of the subjects to receive protocol therapy
4.Subjects with T315I, F317L and V299L BCR-ABL point mutations
5.Subjects with clonal evolution
50
1st name | |
Middle name | |
Last name | Shinya Kimura |
Saga Univ, Faculty of Medicine
Division of Hematology, Respiratory Medicine and Oncology
5-1-1 Nabeshima, Saga, 849-8501
0952-34-2366
1st name | |
Middle name | |
Last name | Shinya Kimura |
DADI-Trial Group
Division of Hematology, Respiratory Medicine and Oncology, Faculty of Medicine, Saga Univ.
shkimu@cc.saga-u.ac.jp
Epidemiological and Clinical Research Information Network (ECRIN)
Epidemiological and Clinical Research Information Network (ECRIN)
Non profit foundation
Japan
NO
佐賀大学医学部(佐賀県)Faculty of Medicine, Saga University
岩手医科大学(岩手県)Iwate Medical University
松下記念病院(大阪府)Matsushita Memorial Hospital
大阪市立大学(大阪府)Osaka City University
名古屋大学医学部(愛知県)Nagoya University School of Medicine
東京都立駒込病院(東京都)Tokyo Metropolitan Cancer and Infectious disease Komagome Hospital
兵庫医科大学(兵庫県)Hyogo College of Medicine
広島市立安佐市民病院(広島県)Hiroshima City Asa Hospital
2011 | Year | 03 | Month | 01 | Day |
Unpublished
No longer recruiting
2011 | Year | 01 | Month | 07 | Day |
2011 | Year | 03 | Month | 01 | Day |
2016 | Year | 03 | Month | 31 | Day |
2011 | Year | 02 | Month | 24 | Day |
2012 | Year | 09 | Month | 05 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006101