Adjuvant Bortezomib Maintenance Therapy After Autologous Peripheral Stem Cell Transplantation in Treating Patients With Intermediate or Advanced Multiple Myeloma

Jonsson Comprehensive Cancer Center

Status and phase

Completed

Phase 2

Phase 1

Conditions

Multiple Myeloma and Plasma Cell Neoplasm

Treatments

Drug: bortezomib

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00084747

CDR0000365583

MILLENNIUM-MM2003

UCLA-0306106

Details and patient eligibility

About

RATIONALE: Bortezomib may stop the growth of cancer cells by blocking the enzymes necessary for their growth. Giving bortezomib as maintenance therapy after autologous stem cell transplantation may kill more cancer cells and prolong remission.

PURPOSE: This phase I/II trial is studying the side effects and best dose of adjuvant bortezomib as maintenance therapy and to see how well it works in treating patients who have undergone stem cell transplantation for intermediate or advanced multiple myeloma.

Full description

OBJECTIVES:

Determine response rate, as defined by resolution of bone marrow plasmacytosis and monoclonal paraproteinemia, in the first year after autologous peripheral blood stem cell transplantation in patients with intermediate or advanced multiple myeloma treated with adjuvant bortezomib.
Compare progression-free survival of patients treated with adjuvant bortezomib with historical controls treated with autologous transplantation alone.
Determine the toxicity of this drug in these patients (phase I).

OUTLINE: This is a multicenter, dose-escalation study.

Patients receive bortezomib IV on days 1, 8, and 15. Treatment repeats every 28 days for 8 courses in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of bortezomib until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 3-30 patients will be accrued for this study within 2 years.

Enrollment

30 patients

Sex

All

Ages

18 to 69 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosis of intermediate or advanced multiple myeloma meeting criteria for at least 1 2 following:
Intermediate- to high-M-component production rates (immunoglobulin [Ig]G > 5 g/dL or immunoglobulin A (IgA) > 3 g/dL or urine M component > 4 g/24 hours)
More than one osteolytic bone lesion or radiographic evidence of diffuse osteoporosis
β-2 microglobulin > 3
Nonsecretory myeloma if bone marrow plasmacytosis is greater than 30%
Must have undergone autologous peripheral blood stem cell transplantation within the past 3-4 months
Age 18 to 69 years old
Absolute neutrophil count ≥ 1,000/mm^3
Platelet count ≥ 30,000/mm^3
serum glutamate oxaloacetate transaminase (SGOT) or serum glutamate pyruvate transaminase (SGPT) ≤ 300 IU
Bilirubin ≤ 2 mg/dL
Creatinine ≤ 2.0 mg/dL
Creatinine clearance ≥ 30 mL/min
Negative pregnancy test
Fertile patients must use effective contraception

Exclusion criteria

concurrent major cardiac disease that would preclude study participation
concurrent major pulmonary disease that would preclude study participation
pregnant or nursing
peripheral neuropathy ≥ grade 2
history of hypersensitivity to bortezomib, boron, or mannitol
concurrent major gastrointestinal or bladder disease that would preclude study participation
concurrent major neurologic or psychiatric disease that would preclude study participation
dementia or significantly altered mental status that would preclude giving informed consent
prior interferon post-transplantation
prior thalidomide post-transplantation
prior chemotherapy post-transplantation
prior radiotherapy post-transplantation
prior investigational therapy post-transplantation
prior bortezomib
prior therapy for myeloma post-transplantation
other concurrent anti-myeloma therapy
other concurrent investigational therapy