Unique ID issued by UMIN | UMIN000019361 |
---|---|
Receipt number | R000022305 |
Scientific Title | Safety and efficacy of BV-ESHAP therapy for relapsed and refractory Hodgkin's lymphoma before transplantation |
Date of disclosure of the study information | 2015/10/16 |
Last modified on | 2016/10/17 11:17:35 |
Safety and efficacy of BV-ESHAP therapy for relapsed and refractory Hodgkin's lymphoma before transplantation
BV-ESHAP for relapsed and refractory Hodgkin's lymphoma
Safety and efficacy of BV-ESHAP therapy for relapsed and refractory Hodgkin's lymphoma before transplantation
BV-ESHAP for relapsed and refractory Hodgkin's lymphoma
Japan |
Hodgkin's lymphoma
Hematology and clinical oncology |
Malignancy
NO
Examine safety and efficacy of BV-ESHAP therapy for refractory and relapsed Hodgkin's lymphoma before transplantation
Safety,Efficacy
Phase II
overall response rate after therapy
(CR and PR on PET-CT)
collected number of CD34 positive cells/adverse events/Overall survival/relapse-free survival
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
3 to 4 courses of BV therapy(1 course for 21 days)
<BV therapy>
BV 1.8mg/kg day1
Consequently, 1 to 2 courses of ESHAP therapy (1 course for 21 to 28 days)
<ESHAP therapy>
ETP 40mg/m^2 1h div day1,2,3,4
CDDP 25mg/m^2 24hr cont day1,2,3,4
AraC 2g/m^2 2hrs day5
mPSL 500mg/day 30min div day1,2,3,4,5
Administer G-CSF from day7.
Collect peripheral blood stem cells.
16 | years-old | <= |
70 | years-old | >= |
Male and Female
CD30 positive lymphoma cells are confirmed and met all the follows:
Announced that patient is Hodgkin's lymphoma.
Considered that Hodgkin's lymphoma is refractory or relapsed.
Eligible for autologous transplantation.
Performance status is 0 to 3.
Have any calculable lesion radiographically.
AST, ALT is under 2.5 times upper limit of normal controls, and total bilirubin is under 2.0 mg/dl.
Creatinine is under 1.5 mg/dl.
Showed no severe abnormalities on echocardiograms and ultrasonic cardiography.
Showed no interstitial pneumonia.
Have written consents from the patient.
For those under 20 years old, written consents of both the patient and his replacement is required.
AST, ALT is over 2.5 times upper limit of normal controls, or total bilirubin is over 2.0mg/dl.(exclude for abnormal due to primary disease)
Creatinine is over 1.5 mg/dl.
Showed severe abnormalities on echocardiograms or ultrasonic cardiography, or congestive heart failure.
Have severe interstitial pneumonia, or past history of interstitial pneumonia.
Allergic to etoposide, cytarabine, cisplatin, or G-CSF.
HIV antibody or HBV-DNA is positive.
Have severe uncontrollable disease(for example, cerebral disease, diabetes mellitus, or severe psychological diseases).
Considered as inadequate for this study by study director, or members of this study.
35
1st name | |
Middle name | |
Last name | Takayuki Shimizu |
Keio University
Department of Hematology
35, Shinanomachi, Shinjuku-ku, Tokyo
03-3353-1211
taka-sh@keio.jp
1st name | |
Middle name | |
Last name | Takayuki Shimizu |
Keio University
Department of Hematology
35, Shinanomachi, Shinjuku-ku, Tokyo
03-3353-1211
taka-sh@keio.jp
Department of Hematology, Keio University
Department of Hematology, Keio University
Self funding
NO
2015 | Year | 10 | Month | 16 | Day |
Unpublished
Terminated
2015 | Year | 10 | Month | 06 | Day |
2015 | Year | 10 | Month | 06 | Day |
2016 | Year | 02 | Month | 28 | Day |
2016 | Year | 02 | Month | 28 | Day |
2016 | Year | 02 | Month | 28 | Day |
2016 | Year | 02 | Month | 28 | Day |
2015 | Year | 10 | Month | 15 | Day |
2016 | Year | 10 | Month | 17 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022305