Bortezomib, Combination Chemotherapy, and Rituximab as First-Line Therapy in Treating Patients With Stage III or Stage IV Follicular Non-Hodgkin's Lymphoma

• Status: Completed
• Trial end date: 2012-01-01
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cyclophosphamide, vincristine, and prednisone, 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 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. Giving bortezomib together with combination chemotherapy and rituximab may kill more cancer cells.

PURPOSE: This phase II trial is studying the side effects and how well giving bortezomib together with combination chemotherapy and rituximab works when given as first-line therapy in treating patients with stage III or stage IV follicular non-Hodgkin's lymphoma.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: NCIC Clinical Trials Group
• Treatments: Bortezomib; Cyclophosphamide; Prednisone; Rituximab; Vincristine

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed follicular non-Hodgkin's lymphoma meeting the following criteria:

• Stage III or IV disease

• Grade 1, 2, or 3 disease requiring systemic first-line treatment

• No transformation to diffuse large cell lymphoma

• At least 1 bidimensionally measurable lesion meeting 1 of the following criteria:

• Lymph nodes > 1.5 cm x 1.0 cm by physical exam or CT scan

• Other non-nodal lesion ≥ 1.0 cm x 1.0 cm by MRI or CT scan OR ≥ 1.0 cm x 1.0 cm (e.g., skin lesions or nodules) by physical exam

• Must have a medical indication for treatment, as indicated by 1 of the following:

• Presence of constitutional symptoms that are attributed to lymphoma (e.g., B symptoms, including night sweats, fever, weight loss, fatigue, or pain)

• Lymphadenopathy that requires treatment based on presence of associated symptoms, potential threat to organ function (e.g., ureteric compromise from retroperitoneal disease), or degree of enlargement (i.e., > 5 cm)

• Impairment of normal organ function (e.g., impaired hematopoiesis due to marrow involvement by lymphoma or from splenomegaly and hypersplenism)

• Immune-related complications of lymphoma that require therapy

• Rate of disease progression for which observation is deemed inappropriate

• No history of any other lymphoproliferative disorder or evidence of transformation to an aggressive histology lymphoma

• No known CNS involvement by lymphoma

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2

• Life expectancy ≥ 12 weeks

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• Platelet count ≥ 75,000/mm^3*

• Absolute neutrophil count ≥ 1,000/mm^3*

• Creatinine ≤ 1.5 times upper limit of normal (ULN)

• Bilirubin ≤ 1.5 times ULN

• AST or ALT ≤ 2.5 times ULN (5 times ULN if liver involvement with lymphoma)

• Able (i.e., sufficiently fluent) and willing to complete the quality of life questionnaires in either English or French

• Inability (illiteracy in English or French, loss of sight, or other equivalent reason) to complete the questionnaires will not make the patient ineligible for the study

• No history of other malignancies, except for the following:

• Adequately treated nonmelanoma skin cancer

• Curatively treated in situ cancer of the cervix

• Ductal carcinoma in situ of the breast (as long as radiation limitation is not exceeded)

• Other solid tumors curatively treated with no evidence of disease for > 5 years

• No history of allergic reactions attributed to compounds containing boron or mannitol

• No history of an unusual or severe allergic reaction to rituximab or similar agent

• No pre-existing neuropathy ≥ grade 2

• No known HIV infection

• No other serious illness or medical condition that would preclude study participation, including any of the following:

• Active, uncontrolled bacterial, fungal, or viral infection

• Significant cardiac dysfunction

• Cardiovascular disease NOTE: *Exceptions will be allowed for values below these thresholds in patients with marrow involvement by lymphoma or lymphoma-related hypersplenism

PRIOR CONCURRENT THERAPY:

• No prior systemic therapy for lymphoma

• No prior bortezomib, cyclophosphamide, or vincristine

• At least 4 weeks since prior radiotherapy that involved ≤ 25% of functioning bone marrow and recovered

• Exceptions may be made for low-dose, nonmyelosuppressive radiotherapy or if the irradiated field is not a significant marrow-bearing area

• At least 2 weeks since prior major surgery

• No other concurrent anticancer therapy, investigational agents, corticosteroids (except for physiologic replacement or antiemesis), cytotoxic chemotherapy, or immunotherapy