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lack of funding
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Phase 2 single-institution trial of early systemic central nervous system prophylaxis in high-risk diffuse large B-cell lymphoma
This is a prospective phase 2 clinical trial of systemic central nervous system prophylaxis among patients with diffuse large B-cell lymphoma at high risk of central nervous system recurrence. The main objective is to evaluate safety and efficacy of early institution of intensive central nervous system prophylaxis in a high-risk group to minimize the risk of a devastating central nervous system recurrence. Patients receive standard primary immunochemotherapy with an addition of planned central nervous system prophylaxis courses on or around day 15 of cycles 2, 4, and 6. Growth factor support and Pneumocystis jirovecii prophylaxis is required. The primary endpoint of this pilot study is protocol-defined toxicity, whereas efficacy (cumulative incidence of central nervous system recurrence) will be a secondary endpoint.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CNS prophylaxis protocol | Experimental | Patients will receive central nervous system prophylaxis protocol using high-dose methotrexate and cytarabine. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Methotrexate | Drug | Systemic methotrexate |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Proportion with clinically significant toxicity | Clinically significant toxicity as defined in the protocol | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative incidence of central nervous system recurrence | Cumulative incidence of central nervous system recurrence | 2 years |
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Inclusion Criteria:
New diagnosis of diffuse large B-cell lymphoma, planned first-line therapy using the standard rituximab- and anthracycline-containing regimens
No central nervous system involvement on initial staging
Performance status of 0 or 1 (Eastern Cooperative Oncology Group scale)
Renal function: creatinine clearance >45 ml/min
Not pregnant; agreeable to contraception
Written informed consent
High risk for central nervous system recurrence as determined by one of the following high-risk features:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Adam J Olszewski, MD | Rhode Island Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Roxanne Wood | Providence | Rhode Island | 02903 | United States |
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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 |
|---|---|
| D008727 | Methotrexate |
| D003561 | Cytarabine |
| ID | Term |
|---|---|
| D000630 | Aminopterin |
| D011622 | Pterins |
| D011621 | Pteridines |
| D006574 | Heterocyclic Compounds, 2-Ring |
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| Cytarabine | Drug | Systemic cytarabine |
|
|
| D009369 |
| Neoplasms |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D000072471 |
| Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
| D003562 | Cytidine |
| D011741 | Pyrimidine Nucleosides |
| D011743 | Pyrimidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D001087 | Arabinonucleosides |
| D009705 | Nucleosides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |