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Chemotherapy and Rituximab With or Without Total-Body Irradiation and Peripheral Stem Cell Transplant in Treating Patients With Lymphoma

Risk-Adapted Therapy for Patients With Untreated Age-Adjusted International Prognostic Index II or III Diffuse Large B Cell Lymphoma

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00039195
Enrollment
98
Registered
2003-01-27
Start date
2006-11-30
Completion date
2010-01-31
Last updated
2016-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lymphoma

Keywords

stage I adult diffuse large cell lymphoma, stage III adult diffuse large cell lymphoma, stage IV adult diffuse large cell lymphoma, contiguous stage II adult diffuse large cell lymphoma, noncontiguous stage II adult diffuse large cell lymphoma

Brief summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Combining chemotherapy with monoclonal antibody therapy, total-body irradiation, and peripheral stem cell transplant may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells. PURPOSE: This phase II trial is studying how well giving chemotherapy with rituximab followed by combination chemotherapy with or without rituximab, total-body irradiation, and peripheral stem cell transplant works in treating patients with lymphoma.

Detailed description

OUTLINE: Patients are stratified according to risk (low-intermediate vs high-intermediate or high). Patients receive induction chemotherapy comprising cyclophosphamide IV, doxorubicin IV over 15 minutes, and vincristine IV over 1-2 minutes on day 1; oral prednisone once daily on days 1-5; and filgrastim (G-CSF) subcutaneously (SC) once daily on days 7-11 or PEG-filgrastim once at least 24 hours after infusion. Patients also receive rituximab IV 2-3 days apart for a total of 2 doses during the week prior to the first course of chemotherapy and on day 1 of courses 2-4 of chemotherapy. Treatment repeats every 14 days for a total of 4 courses in the absence of disease progression or unacceptable toxicity. After the completion of induction chemotherapy, patients undergo CT scan and positron emission tomography (PET) scanning. If the PET scan is positive in one or more nodal sites, a repeat biopsy is performed. Patients with a negative PET scan OR a negative repeat biopsy (including no evidence of lymphoma on repeat bone marrow biopsy) are assigned to receive regimen A for consolidation therapy. Patients with a positive repeat biopsy are assigned to receive regimen B for consolidation therapy. * Regimen A: Patients receive consolidation chemotherapy comprising etoposide IV over 1 hour on days 1-3, ifosfamide IV continuously over 24 hours on day 2, carboplatin IV on day 2, and G-CSF SC once daily on days 5-12 or PEG-filgrastim once at least 24 hours after infusion. Treatment repeats every 14 days for a total of 3 courses in the absence of disease progression or unacceptable toxicity. * Regimen B: Patients receive consolidation chemotherapy as in regimen A for 3 courses. Patients also receive rituximab IV on days -3 to -1 of course 3 of chemotherapy. Patients undergo leukapheresis at the completion of course 3 (G-CSF continues from day 5 until the end of leukapheresis). After completion of leukapheresis, patients begin a regimen of high-dose chemoradiotherapy comprising either total body irradiation twice daily on days -10 to -7 and ifosfamide IV over 1 hour and etoposide IV continuously on days -6 to -2 or BEAM chemotherapy comprising carmustine, etoposide, cytarabine, and melphalan. Autologous peripheral blood stem cells (APBSC) are reinfused on day 0. Patients also receive G-CSF SC daily beginning on day 5 and continuing until blood counts recover. Beginning on day 42 post-APBSC, if blood counts have recovered, patients receive rituximab IV once weekly for 4 weeks. Rituximab is repeated beginning on day 180 in the absence of disease progression. Patients who receive consolidation therapy on regimen A are followed at 4-6 weeks after chemotherapy and patients who receive consolidation therapy on regimen B are followed at 90-120 days after transplantation. All patients are followed closely for 5 years and then annually thereafter. PROJECTED ACCRUAL: A total of 40-98 patients will be accrued for this study within 4 years.

Interventions

BIOLOGICALfilgrastim
BIOLOGICALrituximab
DRUGcarboplatin
DRUGcyclophosphamide
DRUGdoxorubicin hydrochloride
DRUGetoposide
DRUGifosfamide
DRUGprednisone
DRUGvincristine sulfate
PROCEDUREperipheral blood stem cell transplantation
RADIATIONradiation therapy

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Bristol-Myers Squibb
CollaboratorINDUSTRY
Genentech, Inc.
CollaboratorINDUSTRY
Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed aggressive diffuse large B-cell lymphoma * CD20-positive disease * Age-adjusted International Prognostic Index II or III defined by the presence of at least 1 of the following: * Karnofsky performance status 10-70% * Lactate dehydrogenase greater than 200 U/L * Stage III or IV disease * Positron emission tomography avid measurable disease * No CNS involvement PATIENT CHARACTERISTICS: Age: * 18 to 64 Performance status: * See Disease Characteristics Life expectancy: * Not specified Hematopoietic: * Absolute neutrophil count greater than 1,000/mm\^3 * Platelet count greater than 50,000/mm\^3 Hepatic: * Bilirubin less than 2.0 mg/dL unless history of Gilbert's disease or pattern consistent with Gilbert's disease * Hepatitis B surface antigen and hepatitis C antibody negative * No chronic, active, or persistent hepatitis Renal: * Creatinine no greater than 1.5 mg/dL OR * Creatinine clearance greater than 60 mL/min * No chronic renal insufficiency Cardiovascular: * Ejection fraction at least 50% by echocardiogram or MUGA scan * No myocardial infarction within the past 6 months * No unstable angina * No cardiac arrhythmias except chronic atrial fibrillation Other: * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective barrier contraception * HIV negative * No other medical illness that would preclude study * No uncontrolled infection * No other malignancy within the past 5 years except curatively treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix PRIOR CONCURRENT THERAPY: Biologic therapy: * No prior biologic therapy for malignancy Chemotherapy: * No prior chemotherapy for malignancy Endocrine therapy: * Prior steroids allowed if received no more than 1 week of therapy Radiotherapy: * No prior radiotherapy for malignancy Surgery: * No prior surgery for malignancy Other: * No other prior therapy for malignancy

Design outcomes

Primary

MeasureTime frameDescription
Progression Free Survival2 yearsKaplan-Meier estimates will be used to verify the progression free survival.

Countries

United States

Participant flow

Participants by arm

ArmCount
Induction R-CHOPac Therapy
Induction R-CHOPac Therapy for patients with B-Cell Lymphoma
98
Total98

Baseline characteristics

CharacteristicInduction R-CHOPac Therapy
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
1 Participants
Age, Categorical
Between 18 and 65 years
97 Participants
Region of Enrollment
United States
98 participants
Sex: Female, Male
Female
42 Participants
Sex: Female, Male
Male
56 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
98 / 98
serious
Total, serious adverse events
20 / 98

Outcome results

Primary

Progression Free Survival

Kaplan-Meier estimates will be used to verify the progression free survival.

Time frame: 2 years

ArmMeasureValue (NUMBER)
Induction R-CHOPac TherapyProgression Free Survival79 percentage of patients progression free

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026