Unique ID issued by UMIN | UMIN000001050 |
---|---|
Receipt number | R000001258 |
Scientific Title | A phase II study of the combination of Rituximab, Mitoxantrone, Etoposide, and Prednisolone for relapsed elderly patients with diffuse large B-cell lymphoma (R-MEP07) |
Date of disclosure of the study information | 2008/03/01 |
Last modified on | 2015/08/27 16:13:13 |
A phase II study of the combination of Rituximab, Mitoxantrone, Etoposide, and Prednisolone for relapsed elderly patients with diffuse large B-cell lymphoma (R-MEP07)
A phase II study of the combination of Rituximab, Mitoxantrone, Etoposide, and Prednisolone for relapsed elderly patients with lymphoma (R-MEP07)
A phase II study of the combination of Rituximab, Mitoxantrone, Etoposide, and Prednisolone for relapsed elderly patients with diffuse large B-cell lymphoma (R-MEP07)
A phase II study of the combination of Rituximab, Mitoxantrone, Etoposide, and Prednisolone for relapsed elderly patients with lymphoma (R-MEP07)
Japan |
Diffuse large B-cell lymphoma
Hematology and clinical oncology |
Malignancy
NO
The pricipal aims of the study are to investigate the efficacy and safety of the combination of rituximab, mitoxantrone, etoposide and prednisolone for relapsed elderly patients with diffuse large B-cell lymphoma.
Safety,Efficacy
Exploratory
Explanatory
Phase II
Overall tumor response
Complete response, three-year overall survival, three-year progression free survival, treatment related toxicity.
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
R-MEP therapy: rituximab (375mg/m2) on day1 iv, mitoxantrone (6mg/m2) on day2 iv, etoposide (80mg/m2) on day2-6 po and prednisolone (40mg/m2) on day2-6 po. The R-MEP is repeated every 3 weeks for total four cycles.
70 | years-old | <= |
85 | years-old | > |
Male and Female
1) PS (ECOG) 0-2
2) Diffuse large B-cell lymphoma (WHO classification).
Histologically/cytologically proven CD20 positive lymphoma
3) First relapse after prior chemotherapy. Interval of more than 24 weeks from the last chemotherapy
4) Having at least one measurable lesion
5) Well preserved major organ function
6) Cumulative doxorubicin doses <= 400mg/m2
7) Written informed consent
8) Expected survival of => 2 months
1) CNS involvement
2) History of glaucoma
3) History of severe drug allergy
4) Active infectious diseases
5) HIV or HTLV-1 positive
6) HBs antigen or HCV antibody positive
7) Significant complications which include cardiac dysfunction, liver cirrhosis, uncontrolled diabetes, renal failure
8) Interstitial pneumonitis or fibrosis
9) History of other active malignancy
10) Severe mental disorder
11) Regular use of systemic steroids
12) Inadequate physical condition, as diagnosed by primary physician
40
1st name | |
Middle name | |
Last name | Takuya Komeno |
National Hospital Organization Mito Medical Center
Department of Hematology
280 Sakuranosato, Ibaraki-machi, Ibaraki 311-3193 Japan
029-240-7711
t.komeno.d@mn.hosp.go.jp
1st name | |
Middle name | |
Last name | Takuya Komeno |
National Hospital Organization Mito Medical center
Department of Hematology
280 Sakuranosato, Ibaraki-machi, Ibaraki 311-3193 Japan
029-240-7711
t.komeno.d@mn.hosp.go.jp
Clinical Hematology Study Group of National Hospital Organization (CHSG-NHO)
National Hospital Organization
Japan
NO
2008 | Year | 03 | Month | 01 | Day |
Unpublished
Completed
2007 | Year | 11 | Month | 16 | Day |
2007 | Year | 12 | Month | 01 | Day |
2015 | Year | 07 | Month | 30 | Day |
2008 | Year | 02 | Month | 24 | Day |
2015 | Year | 08 | Month | 27 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001258