Samarium Sm 153 Lexidronam Pentasodium Combined With Zoledronic Acid or Pamidronate in Treating Patients With Relapsed or Refractory Multiple Myeloma and Bone Pain

• Status: Completed
• Trial end date: 2008-12-02
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Radioactive drugs, such as samarium Sm 153 lexidronam pentasodium, may carry radiation directly to cancer cells and not harm normal cells. Zoledronic acid and pamidronate may help relieve bone pain caused by multiple myeloma. Giving samarium Sm 153 lexidronam pentasodium together with zoledronic acid or pamidronate may be an effective treatment for multiple myeloma.

PURPOSE: This phase I/II trial is studying the side effects and best dose of samarium Sm 153 lexidronam pentasodium when given together with zoledronic acid or pamidronate and to see how well it works in treating patients with relapsed or refractory multiple myeloma and bone pain.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Mayo Clinic
• Collaborator: National Cancer Institute (NCI)
• Treatments: Diphosphonates; Pamidronate; Samarium ethylenediaminetetramethylenephosphonate; Zoledronic Acid

Criteria

DISEASE CHARACTERISTICS:

• Diagnosis of multiple myeloma

• Relapsed or refractory disease, meeting 1 of the following criteria:

• Recurrent disease after stem cell transplantation

• Recurrent or progressive disease despite treatment with ≥ 1 standard regimen (e.g., an alkylating agent plus glucocorticoid and/or the combination of vincristine, doxorubicin hydrochloride, and dexamethasone)

• Measurable or evaluable disease, defined by at least 1 of the following:

• Monoclonal protein ≥ 1.0 g by serum protein electrophoresis

• Monoclonal protein ≥ 200 mg by 24-hour urine electrophoresis

• Serum immunoglobulin free light chain ≥ 10 mg/dL AND abnormal serum immunoglobulin kappa to lambda free light chain ratio

• Monoclonal bone marrow plasmacytosis ≥ 30% (evaluable disease)

• Patients must have already undergone hematopoietic stem cell collection, if believed to be a transplant candidate OR not eligible for a hematopoietic stem cell transplant

PATIENT CHARACTERISTICS:

• ECOG performance status (PS) 0-2 (ECOG PS 3 allowed if secondary to pain)

• ANC ≥ 1,000/mm^3

• Platelet count ≥ 75,000/mm^3

• Hemoglobin ≥ 8.0 g/dL (transfusions allowed)

• Creatinine ≤ 3 mg/dL

• Calcium < 15 mg/dL

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during and for 4 weeks after completion of study therapy

• No impending long bone fracture

• No active malignancy except for nonmelanoma skin cancer or carcinoma in situ of the cervix or breast

• No uncontrolled infection

• No other co-morbidity that would interfere with the patient's ability to participate in this trial

• No known hypersensitivity to any of the components of samarium Sm 153 lexidronam pentasodium or bisphosphonates

PRIOR CONCURRENT THERAPY:

• Recovered from all prior surgery, radiotherapy, or other antineoplastic therapy

• More than 4 weeks since prior melphalan or other myelosuppressive agents

• More than 2 weeks since prior nonmyelosuppressive agents (e.g., thalidomide or high-dose corticosteroids)

• More than 30 days since prior and no other concurrent investigational therapy

• No prior samarium Sm 153 lexidronam pentasodium or strontium chloride Sr 89

• No concurrent external beam radiotherapy

• No concurrent high-dose corticosteroids

• Concurrent chronic steroids (maximum dose of 20 mg/day prednisone equivalent) allowed for disorders other than myeloma (i.e., adrenal insufficiency or rheumatoid arthritis)

• Low-dose steroids allowed for replacement or inhalation therapy

• No other concurrent medications, including any of the following:

• Cytotoxic chemotherapy

• Systemic antineoplastic therapy including, but not limited to, immunotherapy, hormonal therapy, or monoclonal antibody therapy

• Prophylactic hematopoietic growth factors

• Hematopoietic growth factors allowed for established cytopenia therapy