Table 2.
Agent (Dosage Form) | Clone Sensitivity | Dose Adjustment for eGFR? | Described Kidney-Associated Toxicities | Common Adverse Events | |
B Cell | Plasma Cell | ||||
Proteasome inhibitors | |||||
Bortezomib (IV, SC) | X | X | No | None | Thrombocytopenia |
Peripheral neuropathy | |||||
Varicella zoster reactivation | |||||
Carfilzomib (IV) | X | X | Yes | AKI, thrombotic microangiopathy | Thrombocytopenia |
Dyspnea | |||||
Hypersensitivity reaction | |||||
Varicella zoster reactivation | |||||
Monoclonal antibodies | |||||
Rituximab (anti-CD20) (IV) | X | No | None | Infusion reactions | |
Hepatitis B reactivation | |||||
Daratumumab (anti-CD38) (IV) | X | No | None | Infusion reactions | |
Cytotoxic agents | |||||
Cyclophosphamide (IV, PO) | X | X | No | None | Nausea |
Cytopenias | |||||
Melphalan (IV, PO) | X | X | Yes | None | Nausea |
Cytopenias | |||||
Bendamustine (IV) | X | X | Yes | None | Cytopenias |
Immunomodulatory agents | |||||
Thalidomide (IV, PO) | X | X | No | Hyperkalemia observed in renal insufficiency | Constipation |
Fatigue, somnolence | |||||
Peripheral neuropathy | |||||
Venous thrombosis | |||||
Rash | |||||
Teratogenicity | |||||
Lenalidomide (IV) | X | X | Yes | Increased myelosuppression in renal insufficiency, AKI observed in AL amyloidosis | Cytopenias |
Venous thrombosis | |||||
Diarrhea | |||||
Constipation | |||||
Rash | |||||
Teratogenicity | |||||
Pomalidomide (IV) | X | Unknown | No | Cytopenias | |
Venous thrombosis | |||||
Diarrhea; Constipation | |||||
Teratogenicity | |||||
Other agents | |||||
Fludarabine (IV) | X | Yes | None | Cytopenias | |
Opportunistic infections | |||||
Hemolytic anemia | |||||
Secondary myeloid neoplasms | |||||
Pentostatin (IV) | X | Yes | Increased creatinine | Cytopenias | |
Opportunistic infections | |||||
Hemolytic anemia | |||||
Ibrutinib (PO) | X | Unknown | Increased creatinine | Bleeding | |
Tachyarrhythmias |
IV, intravenous; SC, subcutaneous; PO, oral; AL, amyloid light chain amyloidosis.