INTRODUCTIONMultiple myeloma (MM) is a clonal B-cell disorder characterized by proliferation and accumulation of Blymphocytes and plasma cells in the bone marrow and, more rarely, at extra medullary sites.1 Spine is the bone site that is most frequently affected by MM-related lesions.2 Vertebral lesions can result in pain, permanent deformity, kyphosis, walking impairment, permanent disability, or paralysis. In almost 20% of the cases, spinal cord compression (SCC) may occur; diagnosis and treatment must be carried out rapidly in order to avoid a permanent sensitive or motor defect.
3It can be estimated that over 60% of bone lesions occurring in MM patients involve the spine, as compared with 90% in metastatic prostate cancer, 75% in breast cancer, and 45% in lung cancer. 4 Displacement and compression of the spinal cord can be caused by either epidural invasion by neoplastic tissue or by osseous fragments protruding from a fractured vertebral body. Pain is the first and most common presenting symptom. 5,6 The reason for the pain could be either, mechanical which becomes more intense in case of cough/exercise or radicular pain caused by nerve-root compression. Motor weakness is the second most ABSTRACT Background: Multiple myeloma a plasma cell neoplasm characterized by heterogeneous myriad of presentation with paraparesis or paraplegia in 20% cases due to spinal cord compression by vertebral collapse, compression or fracture. Methods: This is a prospective observational study of thirty transplant ineligible multiple myeloma patients with paraplegia/paraparesis. Pretreatment evaluation done as per standard protocol including MRI whole spine. Involved spine XRT 8Gy single fraction followed by BLD (Bortezomib 1.3mg/m 2 weekly once, Lenalidomide 10mg/m 2 for 21 days, oral dexamethasone 40 mg weekly once). Neurological parameters, time to neurological and tumor response at 6 months assessed. Patients in very good partial response or complete response were maintained on Lenalidomide and bisphosphonate therapy for a period of two years. The duration of symptoms and time to response were analyzed with Mann Whitney Cox test. Results: 15 patients were grade 0 power and others grade 1 or 2. Median time to any neurological response was 2.97 weeks. 63.3% of patients achieved power of grade 5, 30% grade 4 and 6.7% grade 3 powers. 23.3% patients received complete response while 63.3% patient's very good partial response. Conclusions: Bedridden myeloma patients had an excellent improvement in quality of life and tumor control with this treatment schedule.