NCT00075725 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG000
- title
- Dexamethasone and Capizzi Methotrexate Patients < 10 Years
- description
- Patients non-randomly assigned to the DH (High Dose) regimen based on one (or more) of the following characteristics: (1) CNS3 status at entry, (2) testicular leukemic involvement at entry, or (3) extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG001
- title
- Dexamethasone, High Dose Methotrexate (Non Randomly Assigned)
- description
- Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG002
- title
- Dexamethasone & Capizzi Methotrexate Patients => 10 Years Old
- description
- Patients randomly assigned to the DH regimen based on one (or more) of the following characteristics: (1) No CNS3 status at entry, (2) no testicular leukemic involvement at entry, or (3) no extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG003
- title
- Dexamethasone, High Dose Methotrexate (IM) < 10 Years
- description
- Patients in regimen PC (Prednisone, Capizzi) will receive cytarabine, vincristine sulfate, daunorubicin hydrochloride, and pegaspargase. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG004
- title
- Prednisone, Capizzi Methotrexate <10 Years
- description
- Patients in regimen PC will receive cytarabine, vincristine sulfate, daunorubicin hydrochloride, and pegaspargase. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG005
- title
- Prednisone, Capezzi Methotrexate >= 10 Years
- description
- Patients randomly assigned to the PH (Prednisone, High Dose MTX) regimen receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG006
- title
- Prednisone and High Dose Methotrexate < 10 Yrs Old
- description
- Patients randomly assigned to the PH regimen receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG007
- title
- Prednisone and High Dose Methotrexate >=10 Years
- description
- Patients randomly assigned to the DH regimen based on one (or more) of the following characteristics: (1) No CNS3 status at entry, (2) no testicular leukemic involvement at entry, or (3) no extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG008
- title
- Dexamethasone, High Dose Methotrexate (IM) >= 10 Years
- description
- Patients in regimen PC will receive cytarabine, vincristine sulfate, daunorubicin hydrochloride, and pegaspargase. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG009
- title
- Prednisone, Capezzi Methotrexate (Down's Syndrome)
- description
- Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG010
- title
- Dexamethasone, Capizzi Methotrexate Down Syndrome (Non Random)
- description
- Patients non-randomly assigned to the PH regimen based on one (or more) of the following: (1) CNS3 status at entry, (2) testicular leukemic involvement at entry, or (3) extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal MTX in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG011
- title
- Prednisone and High Dose Methotrexate (Non Randomly Assigned)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 6
- group Id
- FG001
- num Subjects
- 6
- group Id
- FG002
- num Subjects
- 20
- group Id
- FG003
- num Subjects
- 8
- group Id
- FG004
- num Subjects
- 4
- group Id
- FG005
- num Subjects
- 38
- group Id
- FG006
- num Subjects
- 3
- group Id
- FG007
- num Subjects
- 51
- group Id
- FG008
- num Subjects
- 15
- group Id
- FG009
- num Subjects
- 4
- group Id
- FG010
- num Subjects
- 2
- group Id
- FG011
- num Subjects
- 2
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 5
- group Id
- FG002
- num Subjects
- 10
- group Id
- FG003
- num Subjects
- 2
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 25
- group Id
- FG006
- num Subjects
- 4
- group Id
- FG007
- num Subjects
- 22
- group Id
- FG008
- num Subjects
- 14
- group Id
- FG009
- num Subjects
- 4
- group Id
- FG010
- num Subjects
- 3
- group Id
- FG011
- num Subjects
- 0
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 4
- group Id
- FG003
- num Subjects
- 1
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 13
- group Id
- FG006
- num Subjects
- 2
- group Id
- FG007
- num Subjects
- 4
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 6
- group Id
- FG002
- num Subjects
- 5
- group Id
- FG003
- num Subjects
- 8
- group Id
- FG004
- num Subjects
- 4
- group Id
- FG005
- num Subjects
- 19
- group Id
- FG006
- num Subjects
- 3
- group Id
- FG007
- num Subjects
- 17
- group Id
- FG008
- num Subjects
- 5
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 1
- group Id
- FG011
- num Subjects
- 0
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 1
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 1
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Pregnancy
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 3
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 2
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 2
- group Id
- FG008
- num Subjects
- 3
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 1
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 12
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 6
- group Id
- FG003
- num Subjects
- 10
- group Id
- FG004
- num Subjects
- 6
- group Id
- FG005
- num Subjects
- 27
- group Id
- FG006
- num Subjects
- 7
- group Id
- FG007
- num Subjects
- 31
- group Id
- FG008
- num Subjects
- 10
- group Id
- FG009
- num Subjects
- 2
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 17
- group Id
- FG001
- num Subjects
- 5
- group Id
- FG002
- num Subjects
- 33
- group Id
- FG003
- num Subjects
- 6
- group Id
- FG004
- num Subjects
- 21
- group Id
- FG005
- num Subjects
- 59
- group Id
- FG006
- num Subjects
- 20
- group Id
- FG007
- num Subjects
- 46
- group Id
- FG008
- num Subjects
- 21
- group Id
- FG009
- num Subjects
- 4
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 5
- type
- Disease Progression, all other reasons
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 2
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 2
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Patient off treatment
- reasons
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 3
- group Id
- FG003
- num Subjects
- 10
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 17
- group Id
- FG006
- num Subjects
- 6
- group Id
- FG007
- num Subjects
- 9
- group Id
- FG008
- num Subjects
- 10
- group Id
- FG009
- num Subjects
- 1
- group Id
- FG010
- num Subjects
- 2
- group Id
- FG011
- num Subjects
- 4
- type
- Ineligible or wrong diagnosis
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 2
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Pt/Guardian refused RT therapy
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 2
- group Id
- FG005
- num Subjects
- 14
- group Id
- FG006
- num Subjects
- 2
- group Id
- FG007
- num Subjects
- 5
- group Id
- FG008
- num Subjects
- 3
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Pt non compliant with therapy
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 246
- group Id
- FG001
- num Subjects
- 106
- group Id
- FG002
- num Subjects
- 296
- group Id
- FG003
- num Subjects
- 246
- group Id
- FG004
- num Subjects
- 232
- group Id
- FG005
- num Subjects
- 710
- group Id
- FG006
- num Subjects
- 246
- group Id
- FG007
- num Subjects
- 696
- group Id
- FG008
- num Subjects
- 302
- group Id
- FG009
- num Subjects
- 34
- group Id
- FG010
- num Subjects
- 12
- group Id
- FG011
- num Subjects
- 28
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 172
- group Id
- FG001
- num Subjects
- 57
- group Id
- FG002
- num Subjects
- 175
- group Id
- FG003
- num Subjects
- 168
- group Id
- FG004
- num Subjects
- 166
- group Id
- FG005
- num Subjects
- 397
- group Id
- FG006
- num Subjects
- 171
- group Id
- FG007
- num Subjects
- 401
- group Id
- FG008
- num Subjects
- 185
- group Id
- FG009
- num Subjects
- 16
- group Id
- FG010
- num Subjects
- 3
- group Id
- FG011
- num Subjects
- 10
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 74
- group Id
- FG001
- num Subjects
- 49
- group Id
- FG002
- num Subjects
- 121
- group Id
- FG003
- num Subjects
- 78
- group Id
- FG004
- num Subjects
- 66
- group Id
- FG005
- num Subjects
- 313
- group Id
- FG006
- num Subjects
- 75
- group Id
- FG007
- num Subjects
- 295
- group Id
- FG008
- num Subjects
- 117
- group Id
- FG009
- num Subjects
- 18
- group Id
- FG010
- num Subjects
- 9
- group Id
- FG011
- num Subjects
- 18
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG000
- title
- Dexamethasone and Capizzi Methotrexate Patients < 10 Years
- description
- Patients non-randomly assigned to the DH (High Dose) regimen based on one (or more) of the following characteristics: (1) CNS3 status at entry, (2) testicular leukemic involvement at entry, or (3) extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG001
- title
- Dexamethasone, High Dose Methotrexate (Non Randomly Assigned)
- description
- Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG002
- title
- Dexamethasone & Capizzi Methotrexate Patients => 10 Years Old
- description
- Patients randomly assigned to the DH regimen based on one (or more) of the following characteristics: (1) No CNS3 status at entry, (2) no testicular leukemic involvement at entry, or (3) no extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG003
- title
- Dexamethasone, High Dose Methotrexate (IM) < 10 Years
- description
- Patients in regimen PC (Prednisone, Capizzi) will receive cytarabine, vincristine sulfate, daunorubicin hydrochloride, and pegaspargase. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG004
- title
- Prednisone, Capizzi Methotrexate <10 Years
- description
- Patients in regimen PC will receive cytarabine, vincristine sulfate, daunorubicin hydrochloride, and pegaspargase. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG005
- title
- Prednisone, Capezzi Methotrexate >= 10 Years
- description
- Patients randomly assigned to the PH (Prednisone, High Dose MTX) regimen receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG006
- title
- Prednisone and High Dose Methotrexate < 10 Yrs Old
- description
- Patients randomly assigned to the PH regimen receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG007
- title
- Prednisone and High Dose Methotrexate >=10 Years
- description
- Patients randomly assigned to the DH regimen based on one (or more) of the following characteristics: (1) No CNS3 status at entry, (2) no testicular leukemic involvement at entry, or (3) no extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG008
- title
- Dexamethasone, High Dose Methotrexate (IM) >= 10 Years
- description
- Patients in regimen PC will receive cytarabine, vincristine sulfate, daunorubicin hydrochloride, and pegaspargase. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal methotrexate in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG009
- title
- Prednisone, Capezzi Methotrexate (Down's Syndrome)
- description
- Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. Dexamethasone (5 mg/m2/dose on Days 1-14 by mouth or infusion twice a day in weeks 1 and 2; intrathecal methotrexate (Aged based dosing: Age (yrs) Dose 1 - 1.99 8 mg 2 - 2.99 10 mg 3 - 8.99 12 mg ≥ 9 15 mg) on days 8 and 29 (CNS3 also on days 15 \& 22) and an injection of pegaspargase (2500 International units/m2 x 1 dose on Day 4, 5 or 6).
- id
- FG010
- title
- Dexamethasone, Capizzi Methotrexate Down Syndrome (Non Random)
- description
- Patients non-randomly assigned to the PH regimen based on one (or more) of the following: (1) CNS3 status at entry, (2) testicular leukemic involvement at entry, or (3) extensive pre-treatment with steroids prior to entry. Patients receive intrathecal cytarabine (Age-based dosing: Age (yrs) Dose 1 - 1.99 30 mg 2 - 2.99 50 mg ≥ 3 70 mg) on day 1; infusions of vincristine sulfate 1.5 mg/m2/dose (maximum dose of 2 mg) on Days 1, 8, 15 and 22 and daunorubicin hydrochloride (25 mg/m2/dose on Days 1, 8, 15 and 22. They will also receive prednisone by mouth or infusion twice a day in weeks 1-4 and intrathecal MTX in weeks 2 and 5. Some patients in all groups may receive induction therapy for 2 additional weeks. Beginning in week 6 or 7, patients may receive combination chemotherapy (vincristine sulfate, dexamethasone, doxorubicin hydrochloride, pegaspargase, cyclophosphamide, mercaptopurine, cytarabine, thioguanine) by infusion, injection, intrathecally, and by mouth for up to 8 weeks.
- id
- FG011
- title
- Prednisone and High Dose Methotrexate (Non Randomly Assigned)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 6
- group Id
- FG001
- num Subjects
- 6
- group Id
- FG002
- num Subjects
- 20
- group Id
- FG003
- num Subjects
- 8
- group Id
- FG004
- num Subjects
- 4
- group Id
- FG005
- num Subjects
- 38
- group Id
- FG006
- num Subjects
- 3
- group Id
- FG007
- num Subjects
- 51
- group Id
- FG008
- num Subjects
- 15
- group Id
- FG009
- num Subjects
- 4
- group Id
- FG010
- num Subjects
- 2
- group Id
- FG011
- num Subjects
- 2
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 5
- group Id
- FG002
- num Subjects
- 10
- group Id
- FG003
- num Subjects
- 2
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 25
- group Id
- FG006
- num Subjects
- 4
- group Id
- FG007
- num Subjects
- 22
- group Id
- FG008
- num Subjects
- 14
- group Id
- FG009
- num Subjects
- 4
- group Id
- FG010
- num Subjects
- 3
- group Id
- FG011
- num Subjects
- 0
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 4
- group Id
- FG003
- num Subjects
- 1
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 13
- group Id
- FG006
- num Subjects
- 2
- group Id
- FG007
- num Subjects
- 4
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 6
- group Id
- FG002
- num Subjects
- 5
- group Id
- FG003
- num Subjects
- 8
- group Id
- FG004
- num Subjects
- 4
- group Id
- FG005
- num Subjects
- 19
- group Id
- FG006
- num Subjects
- 3
- group Id
- FG007
- num Subjects
- 17
- group Id
- FG008
- num Subjects
- 5
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 1
- group Id
- FG011
- num Subjects
- 0
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 1
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 1
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Pregnancy
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 3
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 2
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 2
- group Id
- FG008
- num Subjects
- 3
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 1
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 12
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 6
- group Id
- FG003
- num Subjects
- 10
- group Id
- FG004
- num Subjects
- 6
- group Id
- FG005
- num Subjects
- 27
- group Id
- FG006
- num Subjects
- 7
- group Id
- FG007
- num Subjects
- 31
- group Id
- FG008
- num Subjects
- 10
- group Id
- FG009
- num Subjects
- 2
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 17
- group Id
- FG001
- num Subjects
- 5
- group Id
- FG002
- num Subjects
- 33
- group Id
- FG003
- num Subjects
- 6
- group Id
- FG004
- num Subjects
- 21
- group Id
- FG005
- num Subjects
- 59
- group Id
- FG006
- num Subjects
- 20
- group Id
- FG007
- num Subjects
- 46
- group Id
- FG008
- num Subjects
- 21
- group Id
- FG009
- num Subjects
- 4
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 5
- type
- Disease Progression, all other reasons
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 2
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 2
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Patient off treatment
- reasons
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 3
- group Id
- FG003
- num Subjects
- 10
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 17
- group Id
- FG006
- num Subjects
- 6
- group Id
- FG007
- num Subjects
- 9
- group Id
- FG008
- num Subjects
- 10
- group Id
- FG009
- num Subjects
- 1
- group Id
- FG010
- num Subjects
- 2
- group Id
- FG011
- num Subjects
- 4
- type
- Ineligible or wrong diagnosis
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 2
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Pt/Guardian refused RT therapy
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 2
- group Id
- FG005
- num Subjects
- 14
- group Id
- FG006
- num Subjects
- 2
- group Id
- FG007
- num Subjects
- 5
- group Id
- FG008
- num Subjects
- 3
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Pt non compliant with therapy
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 246
- group Id
- FG001
- num Subjects
- 106
- group Id
- FG002
- num Subjects
- 296
- group Id
- FG003
- num Subjects
- 246
- group Id
- FG004
- num Subjects
- 232
- group Id
- FG005
- num Subjects
- 710
- group Id
- FG006
- num Subjects
- 246
- group Id
- FG007
- num Subjects
- 696
- group Id
- FG008
- num Subjects
- 302
- group Id
- FG009
- num Subjects
- 34
- group Id
- FG010
- num Subjects
- 12
- group Id
- FG011
- num Subjects
- 28
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 172
- group Id
- FG001
- num Subjects
- 57
- group Id
- FG002
- num Subjects
- 175
- group Id
- FG003
- num Subjects
- 168
- group Id
- FG004
- num Subjects
- 166
- group Id
- FG005
- num Subjects
- 397
- group Id
- FG006
- num Subjects
- 171
- group Id
- FG007
- num Subjects
- 401
- group Id
- FG008
- num Subjects
- 185
- group Id
- FG009
- num Subjects
- 16
- group Id
- FG010
- num Subjects
- 3
- group Id
- FG011
- num Subjects
- 10
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 74
- group Id
- FG001
- num Subjects
- 49
- group Id
- FG002
- num Subjects
- 121
- group Id
- FG003
- num Subjects
- 78
- group Id
- FG004
- num Subjects
- 66
- group Id
- FG005
- num Subjects
- 313
- group Id
- FG006
- num Subjects
- 75
- group Id
- FG007
- num Subjects
- 295
- group Id
- FG008
- num Subjects
- 117
- group Id
- FG009
- num Subjects
- 18
- group Id
- FG010
- num Subjects
- 9
- group Id
- FG011
- num Subjects
- 18
- type
- NOT COMPLETED
- title
- Overall Study
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