Bortezomib, Doxorubicin Hydrochloride Liposome, and Rituximab in Treating Patients With Diffuse Large B-Cell Lymphoma That Has Relapsed or Not Responded to Treatment

Roswell Park Comprehensive Cancer Center

Status and phase

Terminated

Phase 2

Conditions

Lymphoma

Treatments

Genetic: polymerase chain reaction

Genetic: polymorphism analysis

Genetic: gene expression analysis

Other: laboratory biomarker analysis

Biological: rituximab

Other: flow cytometry

Genetic: proteomic profiling

Drug: pegylated liposomal doxorubicin hydrochloride

Drug: bortezomib

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00851552

CDR0000635486

RPCI-I-136508

Details and patient eligibility

About

RATIONALE: Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the cancer. Drugs used in chemotherapy, such as doxorubicin hydrochloride liposome, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer cell 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 cell-killing substances to them. Giving bortezomib together with doxorubicin hydrochloride liposome and rituximab may kill more cancer cells.

PURPOSE: This phase II trial is studying how well giving bortezomib together with doxorubicin hydrochloride liposome and rituximab works in treating patients with diffuse large B-Cell lymphoma that has relapsed or not responded to treatment.

Full description

OBJECTIVES:

Primary

To determine the overall objective response rate (i.e., complete and partial response) in patients with relapsed or refractory, CD20-positive, diffuse large B-cell lymphoma treated with bortezomib, pegylated liposomal doxorubicin hydrochloride, and rituximab.

Secondary

To assess the toxicity/safety profile associated with this regimen. To conduct correlative translational research studies.

OUTLINE: Patients receive bortezomib IV on days 1, 4, 8, and 11, pegylated liposomal doxorubicin hydrochloride IV on day 11, and rituximab IV on day 8. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Tissue and blood samples are collected periodically for correlative studies. Samples are analyzed for expression of CD11b/CD18, CD32, CD 33, CD62, CD64, CD69, and CD56 by flow cytometric analysis of neutrophils, NK cells, and monocytes; antibody-dependent cellular and complement-mediated cytotoxicity; and genotypic analysis of polymorphisms by PCR. Autologous neoplastic B-cells derived from tissue samples are used for genetic and protein profiling.

After completion of study therapy, patients are followed periodically for 4 years.

Enrollment

9 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

Diagnosis of CD20-positive diffuse large B-cell lymphoma, including any of the following morphological variants:
- Centroblastic
- Immunoblastic
- T-cell/histiocyte-rich
- Anaplastic
- Mediastinal (thymic) large B-cell lymphoma
- Intravascular large B-cell lymphoma
Relapsed or refractory disease
Measurable disease, defined as tumor size 2 cm²
Must have received ≥ 1 prior standard chemotherapy regimen
No Burkitt or precursor B-lymphoblastic lymphoma
No brain involvement or evidence of CNS lymphoma

PATIENT CHARACTERISTICS:

Karnofsky performance status (PS) 70-100% OR ECOG PS 0-2
Life expectancy ≥ 12 weeks
Absolute neutrophil count ≥ 1,500/μL*
Platelet count ≥ 100,000/μL*
Creatinine < 2.5 mg/dL OR > 40 mL/min*
Hemoglobin > 8.0 g/dL*
AST/ALT < 2 times upper limit of normal (ULN) (< 3 times ULN with liver involvement)*
Alkaline phosphatase < 2 times ULN (< 3 times ULN with liver involvement)*
Total bilirubin < 2 times ULN (< 3 times ULN with liver involvement or Gilbert disease)* NOTE: *Unless attributable to non-Hodgkin lymphoma
LVEF ≥ 50% by MUGA scan or ECHO
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception during and for 6 months after completion of therapy
No HIV positivity
No hepatitis B positivity
Peripheral neuropathy < grade 2 as defined by NCI CTCAE v 3.0
No history of uncontrolled orthostatic hypotension
None of the following cardiac conditions:
- Myocardial infarction within the past 6 months
- New York Heart Association class II-IV congestive heart failure
- Uncontrolled angina
- Severe uncontrolled ventricular arrhythmias
- Clinically significant pericardial disease
- ECG evidence of acute ischemic or active conduction system abnormalities
No hypersensitivity to bortezomib, boron, or mannitol
No history of allergic reactions to compounds containing boron, mannitol, bortezomib, conventional formulation of doxorubicin hydrochloride, or the components of pegylated liposomal doxorubicin hydrochloride
No uncontrolled intercurrent illness including, but not limited to, any of the following:
- Ongoing or active infection
- Poorly controlled hypertension
- Diabetes mellitus
- Serious medical or psychiatric conditions that would interfere with adherence to or completion of this study
No other primary malignancy except squamous cell or basal cell carcinoma of the skin, in situ carcinoma of the cervix, superficial bladder carcinoma, or previously treated localized prostate cancer with normal PSA levels and disease-free for ≥ 5 years

PRIOR CONCURRENT THERAPY:

See Disease Characteristics
Recovered from significant toxicity associated with prior surgery, radiotherapy, chemotherapy, or immunotherapy
Prior rituximab or other monoclonal immunotherapy allowed
More than 4 weeks since prior investigational drugs
More than 4 weeks since prior chemotherapy
More than 4 weeks since prior major surgery, other than diagnostic surgery
No prior doxorubicin hydrochloride (or equivalent) anthracycline treatment exceeding 400 mg/m²
No concurrent corticosteroids, except to control a transient inflammatory reaction (i.e., skin rash or hives)
- Concurrent non-steroidal hormones administered for non-lymphoma related conditions (e.g., insulin for diabetes) allowed
No concurrent radiotherapy
No other concurrent antitumor or chemotherapeutic agents
No other concurrent investigational agents