Phase 2
N=34
Rituximab and Combination Chemotherapy in Treating Patients With Newly Diagnosed, HIV-Associated Burkitt's Lymphoma
Lymphoma
Bottom Line
View on ClinicalTrials.gov: NCT00392834 ↗Enrolled (actual)
34
Serious AEs
67.7%
Results posted
Feb 2013
Primary outcome: Primary: Overall Survival (OS) at 1 Year — 1.0; 0.82 Cumulative proportion surviving at 1 yr
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- filgrastim (Biological); pegfilgrastim (Biological); rituximab (Biological); cyclophosphamide (Drug); cytarabine (Drug); doxorubicin hydrochloride (Drug); etoposide (Drug); ifosfamide (Drug); leucovorin calcium (Drug); liposomal cytarabine (Drug); methotrexate (Drug); therapeutic hydrocortisone (Drug); vincristine sulfate (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- AIDS Malignancy Consortium
- Primary completion
- Jul 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Overall Survival (OS) at 1 Year |
1.0; 0.82 | — |
| SECONDARY Complete Response Rate |
— | — |
| SECONDARY Failure-free Survival (FFS) |
— | — |
| SECONDARY Event-free Survival (EFS) |
— | — |
| SECONDARY Toxicity |
— | — |
| SECONDARY Incidence of Infection-related Deaths |
— | — |
| SECONDARY Correlation of C-flip Expression, p53 Mutations, and Multidrug Resistance Expression With OS, FFS, and EFS |
— | — |
| SECONDARY Utility of Flow Cytometry in Detecting Leptomeningeal Disease |
— | — |
| SECONDARY Degree of Disconcordance Between Flow Cytometry and CNS Cytology Results |
— | — |
| SECONDARY Biologic and Prognostic Significance of Epstein-Barr Virus (EBV) at Diagnosis and Correlation With OS, FFS, and EFS |
— | — |
| SECONDARY Correlation of EBV Load Measurements With OS, FFS, and EFS |
— | — |
Summary
RATIONALE: Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving rituximab together with combination chemotherapy may kill more cancer cells.
PURPOSE: This phase II trial is studying how well giving rituximab together with combination chemotherapy works in treating patients with newly diagnosed, HIV-associated Burkitt's lymphoma.
Eligibility Criteria
DISEASE CHARACTERISTICS:
- Histologically confirmed Burkitt's lymphoma (BL) or new WHO 2009 criteria B-cell lymphoma unclassified (with features intermediated between difuse large B-cell lymphoma and BL)
- Any stage disease
- Newly diagnosed disease
- Meets 1 of the following criteria for disease risk:
- Low-risk disease, defined by 1 of the following:
- Stage I with a single focus of disease < 10 cm AND normal lactate dehydrogenase (LDH) level
- Totally resected intra-abdominal disease only AND normal LDH post surgery
- High-risk disease, defined as not meeting criteria for low-risk disease
- Measurable or nonmeasurable disease
- HIV-positive confirmed by enzyme-linked immunosorbent assay and Western blot OR by measurable HIV viral load
- No visceral Kaposi's sarcoma
PATIENT CHARACTERISTICS:
- Karnofsky performance status 40-100%
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- LVEF ≥ 50% by MUGA or echocardiogram
- Creatinine ≤ 1.5 mg/dL OR creatinine clearance ≥ 60 mL/min
- Absolute neutrophil count ≥ 1,000/mm³
- Platelet count ≥ 50, 000/mm³ (unless related to lymphoma)*
- Direct bilirubin ≤ 2.0 mg/dL OR total bilirubin ≤ 3.5 mg/dL AND direct bilirubin normal (if elevated bilirubin secondary to antiretroviral therapy)
- AST and ALT ≤ 3 times upper limit of normal
- No other malignancy within the past 5 years except curatively treated cutaneous basal cell or squamous cell carcinoma, carcinoma in situ of the cervix, or cutaneous Kaposi's sarcoma
- No other medical illness unrelated to non-Hodgkin's lymphoma, including any of the following:
- Uncontrolled infection (including opportunistic infection)
- Chronic renal insufficiency
- Myocardial infarction within the past 6 months
- Unstable angina
- Cardiac arrhythmias other than chronic atrial fibrillation
- Patients with active hepatitis B infection are eligible provided they receive concurrent dual antiviral therapy NOTE: *Patients with bone marrow involvement are eligible irrespective of blood count
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- No prior therapy for this disease except for 1 of the following :
- Seven consecutive days of steroids alone or in combination with a non-CHOP regimen necessary for patient stabilization (e.g., cyclophosphamide and steroids steroids for normalization of disease-related hyperbilirubinemia)
- One course of CHOP or fractionated CHOP (e.g. CODOX) with or without rituximab
- No epoetin alfa or filgrastim (G-CSF) within 24 hours of study chemotherapy
- No concurrent zidovudine
Data sourced from ClinicalTrials.gov (NCT00392834). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.