Diffuse Large B Cell Lymphoma Clinical Trial
— BormaOfficial title:
Open-label, Multicenter Phase II Study of Bortezomib for Maintenance Therapy in Patients With High Risk Diffuse Large B Cell Lymphoma
Verified date | October 2020 |
Source | Samsung Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is an Open-labeled, multicenter Phase II study of Bortezomib for maintenance therapy in patients with high risk diffuse large B cell lymphoma (DLBCL). Primary objective is 3 years relapse free survival (RFS) and Secondary objectives are 3 years overall survival (OS), 3 years event free survival (EFS),Toxicities profiles, Quality of Life (FACT&GOG-Ntx)
Status | Active, not recruiting |
Enrollment | 59 |
Est. completion date | October 30, 2021 |
Est. primary completion date | October 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility | Inclusion Criteria: 1. Newly histologically confirmed CD20 positive diffuse large B-cell lymphomas and only Non-GCB type will be included 2. High intermediate or high risk by IPI risk, or Bulky mass = 10cm at diagnosis 3. Complete response is confirmed after six or eight cycles R-CHOP chemotherapy by CT scan with confirmed negative PET-CT based on the Revised International Workshop Criteria. 4. Additional surgery or radiotherapy are accepted 5. Age = 20 6. Performance status (ECOG) = 2 7. Adeqaute renal function: Cr < 2.5 mg/dL 8. Adeqaute liver functions: Transaminase (AST/ALT) < 3 x upper normal value UNV)Bilirubin < 1.5 x UNV Alkaline phosphatase < 5 xUNV 9. Adeqaute BM functions: ANC > 1,000/uL and platelet > 75,000/uL and hemoglobin > 9.0 g/dL 10. Written Informed consent Exclusion Criteria: 1. Tumor response after 6-8 cycles CTx< CR 2. Consider stem cell transplantation 3. Central nervous system (CNS) metastases 4. Pregnant or lactating women, patients of childbearing potential not employing adequate contraception 5. Other serious illness or medical conditions A. Unstable cardiac disease despite treatment, myocardial infarction within 6 months prior to study entry B. History of significant neurologic or psychiatric disorders including dementia or seizures C. Active uncontrolled infection 6. Any other malignancies within the past 5 years except curatively treated non- melanoma skin cancer or in situ carcinoma of cervix uteri. 7. Prior history of allegic reaction to study treatment drugs 8. Peripheral neuropathy grade 2 or worse 9. DLBCL of the testis and primary mediastinal DLBCL |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Samsung Medical Center | Seoul |
Lead Sponsor | Collaborator |
---|---|
Samsung Medical Center | Janssen, LP |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 3years relapse free survival | 3years relapse free survival will be assessed after starting maintenance therapy for 1year and then following up for 3years. | from the date of first drug administration until the date of last follow up, assessed up to 4years | |
Secondary | 3years overall survival | 3years overall survival will be assessed after starting maintenance therapy for 1year and then following up for 3years. | from the date of first drug administration until the date of last follow up, assessed up to 4years | |
Secondary | 3years event free survival | 3years event free survival will be assessed after starting maintenance therapy for 1year and then following up for 3years. | from the date of first drug administration until the date of last follow up, assessed up to 4years | |
Secondary | Toxicity profiles | Safety profiles will be evaluated using NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.0. | from the date of first drug administration until the date of the 30th day after last cycle of chemotherapy | |
Secondary | Quality of life scale | Quality of life will be assessed after starting maintenance therapy for 1year and then following up for 3years by using FACT&GOG-Ntx. | from the date of first drug administration until the date of last follow up, assessed up to 4years |
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