Title

Combination Chemotherapy in Treating Patients With Non-Hodgkin's Lymphoma or Acute Lymphocytic Leukemia
A Pilot Study of Dose Intensification of Methotrexate in Patients With Advanced-Stage (III/IV) Small Non-Cleaved Cell Non-Hodgkins Lymphoma and B-Cell All
  • Phase

    Phase 3
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Study Participants

    83
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells.

PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy in treating patients who have non-Hodgkin's lymphoma or acute lymphocytic leukemia.
OBJECTIVES:

Determine if increasing the methotrexate dose in combination with standard treatment is feasible in patients with advanced small noncleaved cell non-Hodgkin's lymphoma or B-cell acute lymphocytic leukemia.
Assess the toxicity of this intensified therapy in these patients.
Assess the feasibility of treating these patients that have CNS disease at diagnosis with this intensified therapy plus etoposide and ifosfamide.
Assess toxicities and late effects of this intensive therapy on the central nervous system, cardiac function, and fertility in these patients.

OUTLINE: This is a multicenter study. Patients are stratified according to stage and disease (stage III non-Hodgkin's lymphoma (NHL) vs stage IV NHL with no CNS involvement vs stage IV NHL with CNS involvement vs B-cell acute lymphocytic leukemia (B-ALL) with no CNS involvement vs B-ALL with CNS involvement).

Patients receive methotrexate and cytarabine intrathecally on days 1, 4, 11, and 36 (on day 40 for patients with stage IV NHL or B-ALL only) in combination with alternating courses of: A) cyclophosphamide IV every 12 hours for a total of six doses on days 1-3, doxorubicin IV over 30 minutes on day 4, vincristine IV on days 4 and 11, dexamethasone IV or orally twice daily on days 1-5, and filgrastim (G-CSF) subcutaneously (SQ) or IV over 30 minutes beginning on day 5 and continuing until blood counts recover and B) methotrexate IV over 24 hours on day 18, methotrexate intrathecally on day 18, dexamethasone IV or orally twice daily on days 18-22, leucovorin calcium IV or orally every 6 hours for a total of 6 doses on days 20-21, cytarabine IV over 48 hours on days 20-21, and G-CSF SQ or IV over 30 minutes beginning on day 22 and continuing until blood counts recover. Patients with stage III NHL receive at total of 5 courses of treatment (A-B-A-B-A) and patients with stage IV NHL or B-ALL with no CNS involvement receive a total of 6 courses of treatment (A-B-A-B-A-B).

Patients with CNS involvement receive a third course of treatment: C) etoposide IV over 1 hour on days 36-40, ifosfamide IV over 1 hour on days 36-40, oral dexamethasone twice daily on days 36-40, and G-CSF SQ or IV over 30 minutes beginning on day 41 and continuing until blood counts recover. Patients with CNS involvement receive a total of 7 courses of treatment (A-B-C-A-B-A-B).

Patients are followed every 6 months for 4 years and then annually thereafter.

PROJECTED ACCRUAL: A total of 27-80 patients will be accrued for this study over 24 months.
Study Started
Sep 30
2000
Primary Completion
Mar 31
2004
Study Completion
Sep 30
2006
Last Update
Aug 21
2013
Estimate

Biological filgrastim

Given IV

  • Other names: GRANULOCYTE COLONY-STIMULATING FACTOR, r-metHuG-CSF, G-CSF, Neupogen, NSC #614629

Drug cyclophosphamide

Given IV

  • Other names: CTX, Cytoxan, NSC #26271, IND #7089

Drug cytarabine

Given IV

  • Other names: cytosine arabinoside, Ara-C, Cytosar, NSC #638

Drug dexamethasone

Given IV

  • Other names: DECADRON, NSC #034521

Drug doxorubicin hydrochloride

Given IV

  • Other names: Adriamycin, NSC #123127, IND #7038

Drug etoposide

Given IV

  • Other names: VP-16, VePesid, NSC #141540, IND #9197

Drug ifosfamide

Given IV

  • Other names: IFX, IFOS, NSC #109724, IND #7887

Drug leucovorin calcium

Given IV

  • Other names: LCV, Wellcovorin, citrovorum factor, folinic acid, NSC #3590

Drug methotrexate

Given IV

  • Other names: MTX, amethopterin, NSC #740, IND #4291

Drug vincristine sulfate

Given IV

  • Other names: VCR, Oncovin, NSC #67574, IND #7161

STAGE III NHL (Trt 1) Experimental

A: Cyclophosphamide (CTX), Doxorubicin hydrochloride, Vincristine sulfate (VCR), Dexamethasone IT Therapy. B: HD-Methotrexate(MTX), Cytarabine(Ara-C), Dexamethasone IT Therapy. Treatment ABABA

STAGE IV NHL, -CNS (Trt 2) Experimental

A: Cyclophosphamide (CTX), Doxorubicin hydrochloride, Vincristine sulfate (VCR), Dexamethasone IT Therapy. B: HD-Methotrexate(MTX), Cytarabine(Ara-C), Dexamethasone IT Therapy. Treatment ABABAB

STAGE IV, +CNS (Trt 3) Experimental

A: Cyclophosphamide (CTX), Doxorubicin hydrochloride, Vincristine sulfate (VCR), Dexamethasone IT Therapy. B: HD-Methotrexate(MTX), Cytarabine(Ara-C), Dexamethasone IT Therapy. C: Etoposide, Ifosfamide, Dexamethasone IT Therapy. Treatment ABCABAB

B-ALL, -CNS (Trt 2) Experimental

A: Cyclophosphamide (CTX), Doxorubicin hydrochloride, Vincristine sulfate (VCR), Dexamethasone IT Therapy. B: HD-Methotrexate(MTX), Cytarabine(Ara-C), Dexamethasone IT Therapy. Treatment ABABAB

B-ALL, +CNS (Trt 3) Experimental

A: Cyclophosphamide (CTX), Doxorubicin hydrochloride, Vincristine sulfate (VCR), Dexamethasone IT Therapy. B: HD-Methotrexate(MTX), Cytarabine(Ara-C), Dexamethasone IT Therapy. C: Etoposide, Ifosfamide, Dexamethasone IT Therapy. Treatment ABCABAB

Criteria

DISEASE CHARACTERISTICS:

One of the following diagnoses:

Histologically confirmed small noncleaved cell non-Hodgkin's lymphoma

Stage III or IV
Burkitt's or non-Burkitt's by the Working Formulation OR
Burkitt's or Burkitt's-like by the REAL classification

Histologically confirmed B-cell acute lymphocytic leukemia

At least 25% blasts in bone marrow
FAB L3 morphology
FAB L1 morphology allowed if blasts show B-cell markers (CD19, 20, 22) and surface immunoglobulin positivity
Must be registered on POG-9900 in past 8 days

PATIENT CHARACTERISTICS:

Age:

Under 22 at time of diagnosis

Performance status:

Not specified

Life expectancy:

Not specified

Hematopoietic:

Not specified

Hepatic:

Not specified

Renal:

Not specified

Other:

Not pregnant or nursing
Negative pregnancy test
HIV positive allowed

PRIOR CONCURRENT THERAPY:

Biologic therapy:

Not specified

Chemotherapy:

Not specified

Endocrine therapy:

No concurrent use of dexamethasone as antiemetic

Radiotherapy:

Not specified

Surgery:

Prior surgery allowed

Other:

No prior therapy except surgery
No Results Posted