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A phase II trial of ifosfamide, etoposide, cytarabine, and methotrexate (IVAM) chemotherapy for refractory or relapsed diffuse large B cell lymphoma
Diffuse Large B-Cell lymphoma is currently used as a standard treatment, with a combination of chemotherapy (R-CHOP), which includes Rituximab. However, the survival rate is very poor if the primary treatment is refractory or relapsed within a year or less. The duration of these patients ' lives is around one year and the five-year survival rate is 15-20 %. Thus, a new treatment strategy is needed to improve the survival of the patient with DLBCL, which are either refractory and relapsed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| I Ifosfamide, Etoposide, Cytarabine, and Methotrexate (IVAM) | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ifosfamide, Etoposide, Cytarabine, and Methotrexate (IVAM) Chemotherapy | Drug | Every cycle(4weeks) Subject will receive Ifosfamide 1.5 g/m2 over 2 hours for Day1~Day5 by Intravenous infusion, Etoposide 150 mg/m2 over 3 hours on Day1~Day3 by Intravenous infusion, Cytarabine 100 mg/m2 over 1 hour on Day1~Day3 by Intravenous infusion. |
| Measure | Description | Time Frame |
|---|---|---|
| Response | CT, PET-CT(positron emission computed tomography ) | 2 to 3 weeks after completion of the 2nd cycle of treatment (each cycle is 28 days) |
| Measure | Description | Time Frame |
|---|---|---|
| Assess response rate | CT, PET-CT | 4 to 5 weeks after completion of the 4th cycle of treatment(each cycle is 28 days) |
| Assess response rate | CT, PET-CT |
| Measure | Description | Time Frame |
|---|---|---|
| Assess overall survival | CT, PET-CT | The time from the 1st day of treatment to death of any cause or the date of last follow-up, assessed up to 66 months |
Inclusion Criteria:
Written informed consent
Histologically confirmed adult patients diagnosed with DLBCL refractory or relapsed.
Large scale B cell lymphoma not received ASCT(autologous stem-cell transplantation ) after primary chemotherapy
At least one measurable lesion
Performance status: Eastern Cooperative Oncology Group (ECOG) 0-2.
Age 19~59yrs
MUGA(multiple gated acquisition scan ): Non-Clinical significant and 2D-Echo( Cardiac Index ≥ 50 % )
Adequate renal function: serum creatinine level < 2.0 mg/dL(177μmol/L) Adequate liver functions: Transaminase (AST/ALT) < 3 X upper limit of normal value (or < 5 x ULN in the presence of DLBCL involvement of the liver), bilirubin < 2 X upper normal value (or < 5 x upper limit of normal in the presence of DLBCL involvement of the liver)
Adequate hematological function: hemoglobin ≥ 9.0 g/dL absolute neutrophil count (ANC) ≥ 1,500/μL and platelet count ≥ 75,000/μL,
A negative serum or urine pregnancy test prior to treatment must be available both for pre menopausal women and for women who are < 1 years after the onset of menopause.
Exclusion Criteria:
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|
|
| 6 to 8 weeks after completion of the 6th cycle of treatment(each cycle is 28 days) |
| Assess response rate | CT, PET-CT | After completion of the treatment, up to 24weeks |
| Assess response rate | CT, PET-CT | After 1year completion of the treatment up to 1year |
| Assess response rate | CT, PET-CT | Afer 2years completion of the treatment up to 3years |
| 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 |
| D009369 | Neoplasms |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
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| ID | Term |
|---|---|
| D007069 | Ifosfamide |
| D005047 | Etoposide |
| D003561 | Cytarabine |
| D008727 | Methotrexate |
| D004358 | Drug Therapy |
| ID | Term |
|---|---|
| D003520 | Cyclophosphamide |
| D010752 | Phosphoramide Mustards |
| D009588 | Nitrogen Mustard Compounds |
| D009150 | Mustard Compounds |
| D006846 | Hydrocarbons, Halogenated |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D063088 | Phosphoramides |
| D009943 | Organophosphorus Compounds |
| D010078 | Oxazines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D011034 | Podophyllotoxin |
| D013764 | Tetrahydronaphthalenes |
| D009281 | Naphthalenes |
| D011084 | Polycyclic Aromatic Hydrocarbons |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D011083 | Polycyclic Compounds |
| D005960 | Glucosides |
| D006027 | Glycosides |
| D002241 | Carbohydrates |
| D003562 | Cytidine |
| D011741 | Pyrimidine Nucleosides |
| D011743 | Pyrimidines |
| D001087 | Arabinonucleosides |
| D009705 | Nucleosides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |
| D000630 | Aminopterin |
| D011622 | Pterins |
| D011621 | Pteridines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D013812 | Therapeutics |
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