Unique ID issued by UMIN | UMIN000014902 |
---|---|
Receipt number | R000017333 |
Scientific Title | A multicenter phase II study for previouly untreated advanced stage peripheral T-cell lymphoma evaluating efficacy and safety of combination chemotherapy with THP-COP regimen |
Date of disclosure of the study information | 2014/08/20 |
Last modified on | 2014/08/20 13:45:43 |
A multicenter phase II study for previouly untreated advanced stage peripheral T-cell lymphoma evaluating efficacy and safety of combination chemotherapy with THP-COP regimen
A phase II study of THP-COP therapy for previouly untreated advanced stage peripheral T-cell lymphoma.
A multicenter phase II study for previouly untreated advanced stage peripheral T-cell lymphoma evaluating efficacy and safety of combination chemotherapy with THP-COP regimen
A phase II study of THP-COP therapy for previouly untreated advanced stage peripheral T-cell lymphoma.
Japan |
previouly untreated advanced stage peripheral T-cell lymphoma
Hematology and clinical oncology |
Malignancy
NO
A multicenter phase II study in previouly untreated advanced stage peripheral T-cell lymphoma evaluating efficacy and safety of combination chemotherapy with THP-COP regimen
Safety,Efficacy
Exploratory
Pragmatic
Phase II
complete response rate, %CR
1) short-term safety
2) response rate (%RR)
3) 1year progression-free survival (1-y PFS)
4) 1year overall survival (1-y OS)
5)long-term safety
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
Chemotherapy (Age20-69: 8 cycles and 70-79: 6 cycles of R-THP-COP therapy)
20 | years-old | <= |
79 | years-old | >= |
Male and Female
1. Histological confirmed Peripheral T-cell lymphoma including unspecified (PTCL-u), Angioimmunoblatic T-cell lymphoma (AITL) and Anaplastic large cell lymphoma (ALCL) excluding ETL, HSTCL, SPTCL and ATLL (WHO)
2. Clinical stage of bulky II, III or IV according to Ann Arbor classification
3. Aged 20-79 years
4. Performance status of 0-2
5. Presence of measurable lesion(s)
6. No prior chemotherapy, radiotherapy, interferon and/or antibody therapy
7. Patients with sufficient organ functions
8. Patient's written informed consent
1. Presence of central nervous involvement (clinical or pathological)
2. Diabetes mellitus receiving insulin therapy
3. Uncontrollable hypertension
4. History of angina pectoris or myocardial infarction. Comorbidity of cardiomyopathy. Arrhythmia on treatment with antiarrhythmic agents
5. Positive test for HBs antigen
6. Positive test for HCV antibody
7. Positive test for HIV antibody
8. Accompanying interstitial pneumonitis, pulmonary fibrosis or severe emphysema diagnosed by chest X-ray
9. Severe infection
10. Biopsy proven or clinically diagnosed Liver cirrhosis
11. Active double cancer: overlapping cancer or asynchronous cancer within 5 years. Carcinoma in situ, intramucosal cancers, and other equivalent lesions are not included for the active double cancer
12. Use of major tranquilizer, antidepressant or antimanic drugs
13. Severe psychosis
40
1st name | |
Middle name | |
Last name | Michinori Ogura |
National Hospital Organization Suzuka National Hospital
Department of Internal Mediciney & Laboratory Medicine
Kasado 3-2-1, Suzuka, Mie, 513-8501, Japan
059-378-1321
mi-ogura@naa.att.ne.jp
1st name | |
Middle name | |
Last name | Michinori Ogura |
Hematological Malignancy Study Group
Hematological Malignancy Study Group
Kasado 3-2-1, Suzuka, Mie, 513-8501, Japan
059-378-1321
http://www.hmcsg.umin.jp/
mi-ogura@naa.att.ne.jp
Hematological Malignancy Study Group
none
Self funding
NO
2014 | Year | 08 | Month | 20 | Day |
Unpublished
No longer recruiting
2007 | Year | 05 | Month | 12 | Day |
2007 | Year | 10 | Month | 07 | Day |
2015 | Year | 09 | Month | 15 | Day |
2014 | Year | 08 | Month | 20 | Day |
2014 | Year | 08 | Month | 20 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000017333