Table 1.
Inclusion and exclusion criteria
| Inclusion criteria |
| ∘ Age greater than 18 years |
| ∘ Dialysis dependent acute renal failure (defined by: an estimated GFR of < 15 ml/min/1.73 m2) |
| ∘ Fulfils criteria for the diagnosis of symptomatic de novo multiple myeloma |
| ∘ Abnormal serum FLC ratio and a serum FLC concentration > 500 mg/L |
| ∘ Myeloma kidney demonstrated on a renal biopsy (cast nephropathy) |
| ∘ Commencement of study within 10 days of presenting to enrolling unit |
| Exclusion criteria |
| ∘ Known advanced chronic renal failure (eGFR < 30 mls/min/1.73 m2) or evidence of significant chronic damage on renal biopsy |
| ∘ Amyloidosis or light chain deposition disease on renal biopsy |
| ∘ Previous treatment of multiple myeloma with chemotherapy |
| ∘ Haemodynamic instability that precludes unsupported renal replacement therapy |
| ∘ Significant cardiac disease |
| ∘ Advanced disease or significant co-morbidity: with poor short term prognosis, necessitating palliation and no active or disease specific treatment. |
| ∘ History of allergic reaction attributable to compounds containing boron or mannitol |
| ∘ Peripheral neuropathy or neuropathic pain Grade 2 or higher |
| ∘ Clinically significant liver dysfunction (bilirubin > 1.8 mg/dl (30 umol/L)) |
| ∘ Active uncontrolled infection or known HIV infection |
| ∘ Inability to give informed consent |
| ∘ Pregnant and lactating women |