Overview
Combination Chemotherapy Followed by Bone Marrow or Peripheral Stem Cell Transplantation in Treating Patients With Relapsed or Refractory Hodgkin's Lymphoma
Status:
Completed
Completed
Trial end date:
2002-02-01
2002-02-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with bone marrow or peripheral stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy followed by bone marrow or peripheral stem cell transplantation in treating patients with relapsed or refractory Hodgkin's lymphoma.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Temple UniversityTreatments:
Cisplatin
Cyclophosphamide
Etoposide
Etoposide phosphate
Criteria
DISEASE CHARACTERISTICS:- Histologically proven stage I-IV Hodgkin's lymphoma
- Must have refractory or relapsed disease, defined by 1 of the following:
- Failure to achieve a complete remission (CR) after 4 courses of conventional-dose
front-line chemotherapy
- Disease in second or greater remission
- Patients should be encouraged to undergo transplantation prior to a third
salvage regimen
- Patients previously treated with multiple regimens considered on a
case-by-case basis
- No chemoresistant disease, defined as active progression with tumor growth greater
than 25% by volume during first-line chemotherapy
- Patients who respond to second-line chemotherapy may be eligible
- Stable residual masses after conventional-dose chemotherapy not considered treatment
failures
- Active (refractory or relapsed) disease must be proven histologically or
documented by gallium nitrate uptake
- Syngeneic marrow transplantation offered to patients with consenting identical twin
donor
- No CNS involvement by lymphoma
PATIENT CHARACTERISTICS:
Age:
- 15 to 60 (selected patients up to age 70 may be eligible)
Performance status:
- ECOG 0-2
Life expectancy:
- Not specified
Hematopoietic:
- WBC greater than 4,000/mm^3
- Absolute neutrophil count greater than 2,000/mm^3
- Platelet count greater than 100,000/mm^3
Hepatic:
- Bilirubin less than 2.0 mg/dL
- SGOT and SGPT less than 2 times upper limit of normal
- Albumin greater than 3.0 g/dL
Renal:
- Must meet 1 of the following criteria:
- Creatinine less than 1.8 mg/dL
- Creatinine clearance greater than 60 mL/min
- BUN less than 20 mg/dL
Cardiovascular:
- Left ventricular ejection fraction at least 50%
Pulmonary:
- DLCO, FEV_1, and FVC greater than 50% of predicted OR
- Resting pO_2 greater than 70 mm Hg on room air
Other:
- HIV negative
- No severe neurologic or emotional disorders
- No active infection
- No other disease that would limit life expectancy
- Not pregnant
- Fertile patients must use effective contraception
- Adequate psychosocial support required
PRIOR CONCURRENT THERAPY:
Biologic therapy
- Not specified
Chemotherapy
- See Disease Characteristics
Endocrine therapy
- Not specified
Radiotherapy
- Not specified
Surgery
- Not specified