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| Name | Class |
|---|---|
| Consortium for Improving Survival of Lymphoma | OTHER |
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The outcome of patients with central nervous system (CNS) relapse in DLBCL is poor, with median survival times of 2-5 months. This fatal prognosis necessitates CNS prevention in a subgroup of patients with a high risk of CNS relapse.
Intrathecal methotrexate (ITMTX) has traditionally been used, although its efficacy for CNS prophylaxis is contradictory. High-dose intravenous methotrexate (IVMTX) has been suggested as an alternative approach. Considering the lack of evidence supporting the role of ITMTX, the investigators propose to compare the efficacy of ITMTX and IVMTX for prophylaxis of CNS relapse in a subgroup of patients with DLBCL at a high risk for CNS relapse.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intrathecal Methotrexate | Other |
| |
| High-dose Intravenous Methotrexate | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Intrathecal methotrexate | Drug | Intrathecal administration of 2nd, 3rd, and 4th doses of methotrexate 15 mg and hydrocortisone 50mg on day 2 or 3 of 2nd, 3rd, and 4th cycles of immunochemotherapy with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (RCHOP), respectively. |
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative incidence of CNS relapse | The rate of relapse will be analyzed by the cumulative incidence method | 2 year |
| Measure | Description | Time Frame |
|---|---|---|
| Toxicity | Toxicity will be graded according to NCI-CTCAE v.4.03 | 2 year |
| Progression-free survival (PFS) | PFS will be calculated from randomization to the date of CNS relapse and/or systemic disease progression, death, or last follow-up, as appropriate. |
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Inclusion Criteria:
Aged ≥18 years <80
Newly diagnosed, histologically confirmed DLBCL
High-risk of CNS recurrence at diagnosis:
Estimated life expectancy of more than 90 days
Performance status (ECOG) ≤ 2
Written informed consent
Exclusion Criteria:
Psychiatric or mental disorder which make the patient unable to give an informed consent and/or adhere to the protocol
DLBCL or following subtypes:
Previous immunochemotherapeutic treatment for DLBCL other than short-term use of corticosteroids (≤ 8 days before randomization)
Previous radiotherapy
CNS involvement of DLBCL at diagnosis
HIV positive
Any contraindication for application of RCHOP or high dose methotrexate
Any of following laboratory results
Serum creatinine >2.0 x ULN or creatinine clearance <50 mL/min
Active cancer except curable basal cell carcinoma, cervical cancer in situ, and/or papillary thyroid cancer during the last five years
Ejection fraction < 45% on echocardiography
Uncontrolled active hepatitis
Pregnancy or breast-feeding
Men and women of reproductive potential no agreeing to use an acceptable method of birth control during treatment
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Deok-Hwan Yang | Contact | +82-61-379-7636 | drydh1685@hotmail.com | |
| Seung-Ah Yahng | Contact | +82-32-280-5893 | saymd@catholic.ac.kr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chonnam National University Hwasun Hospital | Hwasun-gun | Jeollanam-do | 519-809 | South Korea |
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| High-dose intravenous methotrexate | Drug | Intravenous administration of 1st and 2nd doses of methotrexate 3g/m2 on day 15 of 2nd and 6th cycles of immunochemotherapy with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (RCHOP), respectively. * Dose of intravenous methotrexate will be reduced to 2g/m2 for patients aged >70 years. |
|
| 2 year |