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| Name | Class |
|---|---|
| Samsung Medical Center | OTHER |
| Asan Medical Center | OTHER |
| Severance Hospital | OTHER |
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Rituximab (R) plus CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) combination is considered as the new gold standard for the first-line treatment of elderly patients with diffuse large B-cell lymphoma (DLBCL).
The study is aimed to evaluate the overall response rate and the safety of four cycles of R-CHOP chemotherapy and followed by rituximab augmentation (weekly four times infusion) in newly diagnosed DLBCL patients with aged more than 70 years.
Four cycles of R-CHOP chemotherapy for the induction treatment [Dose intensity of CHOP chemotherapy is modulated according to Charlson Comorbidity Index (CCI)]
If patients with CCI <1
If patients with CCI ≥1
Rituximab augmentation
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| rituximab | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| rituximab | Drug | A dose of 375mg/m2 rituximab will be administered intravenously on day 1 of first to fourth R-CHOP chemotherapy and on day 1, 8, 15, 22 of each augmentation chemotherapy. |
| Measure | Description | Time Frame |
|---|---|---|
| the overall response rate | To evaluate the objective overall response rate of four cycles of R-CHOP and followed by four times weekly rituximab augmentation in exteremely elderly patients with DLBCL. | three years after the completion of rituximab augmentation |
| Number of patients with adverse events | All patients will be evaluated for the toxicity during the treatment. Toxicity is graded according to the National Cancer Institute Common Toxicity Criteria (NCI-CTC v3.0). | three years |
| Measure | Description | Time Frame |
|---|---|---|
| progression-free survival | Three years after the completion of rituximab augmentation |
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Inclusion Criteria:
Histologically confirmed CD20 positive DLBCL
Age ≥ 70
Ann Arbor stage II, III and IV
No prior chemotherapy or radiotherapy for DLBCL
Performance status (Eastern Cooperative Oncology Group) ≤ 2
At least one or more bidimensionally measurable lesion(s)
Cardiac ejection fraction ≥ 50% as measured by echocardiogram without clinically significant abnormalities
Adequate renal function: serum creatinine level < 2 mg/dL (177 μmol/L)
Adequate liver functions:
Adequate bone marrow functions:
hemoglobin ≥ 9 g/dL absolute neutrophil count ≥ 1,500/μL and platelet count ≥ 75,000/μL, unless abnormalities are due to bone marrow involvement by lymphoma
Life expectancy more than 6 months
Informed consent
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Deok-Hwan Yang, M.D. and Ph.D. | Contact | 82-61-379-7636 | drydh1685@gmail.com | |
| Je-Jung Lee, M.D. and Ph.D. | Contact | 82-61-3797638 | drjejung@chonnam.ac.kr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chonnam National University Hwasun Hosptial | Recruiting | Jeollanam-do | 519-809 | South Korea |
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| ID | Term |
|---|---|
| D016403 | Lymphoma, Large B-Cell, Diffuse |
| ID | Term |
|---|---|
| D016393 | Lymphoma, B-Cell |
| D008228 | Lymphoma, Non-Hodgkin |
| D008223 | Lymphoma |
| D009370 | Neoplasms by Histologic Type |
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| ID | Term |
|---|---|
| D000069283 | Rituximab |
| ID | Term |
|---|---|
| D058846 | Antibodies, Monoclonal, Murine-Derived |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
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| D009369 |
| Neoplasms |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D007162 | Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |