Copyright
        ©The Author(s) 2020.
    
    
        World J Clin Oncol. Apr 24, 2020; 11(4): 190-204
Published online Apr 24, 2020. doi: 10.5306/wjco.v11.i4.190
Published online Apr 24, 2020. doi: 10.5306/wjco.v11.i4.190
            Table 1 Relationship between anticancer drug class, its nephrotoxic effects and mechanism of action of its lesion
        
    | Class | Drugs | Nephrotoxicity | Mechanism of action | 
| Alkylating agents | Bendamustine; Cyclophosphamide; Ifosfamide; Melfalano; Nitrosureasnts | AKI; Hemorrhagic cystitis; Inflammatory lesion; SIADH; Hyponatremia; Fanconi's syndrome; Interstitial nephritis; Diabetes | Damage to proximal and distal tubular structures by action of metabolites and increased cellular oxidative stress | 
| Antimetabolites | Chlopharabine; Methotrexate; Pemetrexed; Gemcitabine; Pentostatin | AKI; Decreased GFR; Interstitial edema; Tubular acidosis; Diabetes insipidus; Microangiopathic hemolytic anemia; SIADH; Hyponatremia | Decreased GFR due to vasoconstrictor action on afferent renal arteries; Crystal precipitation in tubules and induction of tubular injury | 
| Anti-microtubular agents | Paclitaxis; Vincristine; Vinblastine; Vinorelbine | SIADH | Inhibits synthesis of genetic material or causes irreparable DNA damage | 
| Antitumor antibiotics | Daunorubicin; Doxorubicin; Mitomycin | Nephrotic syndrome; Focal segmental glomerular sclerosis; TMA; AKI; Hemolytic uremic syndrome | Epithelial lesions (podocytes) | 
| Platinum agents | Cisplatin; Carboplatin; Ocaliplatin | AKI; Anemia; Hypomagnesemia; Proximal tubular dysfunction; TMA | Drug accumulation in the proximal renal tubules | 
| Cytotoxic agents | Arsenic trioxide; Etoposide; Irinotecan; Topotecan | Tubulointerstitial disease; Rhabdomyolysis; AKI | Increased exposure can be toxic; Higher levels of hematologic toxicity | 
| Immunomodulatory drugs | Thalidomide; Lenalidomide; Pomalidomide | Hypercalcemia; Decreased GFR; Nephrolithiasis | Unclear, depending on the drug, may be related to its type of metabolism | 
| Proteasome inhibitors | Bortezomib; Carfilzomib; Ixazomib | TMA; Acute interstitial nephritis; AKI | Prerenal causes (e.g., hypovolemia); Tumor lysis-like syndrome | 
| EGFR pathway inhibitors | Cetuximab; Panitumumab; Afatinib; Erlotinib; Gefitinib | Electrolyte disturbance; AKI; Diffuse proliferative glomerulonephritis; Nephrotic syndrome | Inhibition of EGFR signaling at the distal convoluted tubule, which regulates transepithelial magnesium transport; AKI mechanism is unclear, however, EGFR plays a role in the maintenance of tubular integrity | 
| HER-2 inhibitors | Trastuzumab; Ado-trastuzumab emtansine; Pertuzumab | Proteinuria; AKI; Decreased GFR; Electrolyte disturbance; Hypertension | Unclear | 
| BCL-2 inhibitors | Venetoclax; Obituzumab; Ofatumumab | AKI | Tumor lysis syndrome | 
| ALK inhibitors | Crizotinib; Alectinib; Brigatinib | Decreased GFR; Development of complex renal cysts; Electrolyte disturbance | Unclear | 
| BRAF inhibitors | Vemurafenib; Dabrafenib; Trametinib; Cobimetinib | Decrease GFR; AKI; Glomerulonephritis; Hyponatremia; Hypertension | Unclear | 
| MTOR inhibitors | Temsirolimus | Glomerulopathy; AKI; Proteinuria | Unclear | 
| BCR-ABL1 and KIT inhibitors | Bosutinib; Dasatinib; Imatinib | Hypophosphatemia; Decreased GFR; AKI; Proteinuria; Nephrotic syndrome; CKD | Rhabdomyolysis; Thrombotic thrombocytopenic purpura; Alterations in glomerular podocytes; Tumor lysis syndrome; Acute tubular injury | 
| Anti-angiogenesis drugs (VEGF pathway inhibitors and TKI) | Bevacizumab; Ramucirumab; Aflibercept; Sunitinib; Sorafenib; Pazopanib; Ponatinib; Others | Hypertension; Proteinuria; Nephrotic syndrome; Decreased GFR; TMA; Glomerulopathy; Electrolyte disturbance | Endothelial cell dysfunction and dysregulation of podocyte | 
| Inhibitor of Bruton’s tyrosine kinase | Ibrutinib | AKI | Unclear, but tumor lysis syndrome might be contributory | 
| Immune checkpoint inhibitors (PD-1, PD-L1, CTLA-4) | Ipilimumab; Pembrolizumab; Nivolumab | Acute tubulointerstitial nephritis; Immune complex glomerulonephritis; TMA; Electrolyte disturbance; AKI (rare) | Unclear, but development of autoantibodies that are pathogenic to the kidney might be contributory | 
| Cytokine | INF-a | Proteinuria; Glomerulopathy; TMA; AKI | Minimal change disease or focal segmental glomerulosclerosis | 
| Cytokine | IL-2 | AKI | Capillary leak syndrome leading to AKI | 
| Peptide receptor radioligand | Lutetium Lu-177 dotatate | Decreased GFR | Kidney irradiation | 
- Citation: Santos MLC, Brito BB, da Silva FAF, Botelho ACDS, Melo FF. Nephrotoxicity in cancer treatment: An overview. World J Clin Oncol 2020; 11(4): 190-204
- URL: https://www.wjgnet.com/2218-4333/full/v11/i4/190.htm
- DOI: https://dx.doi.org/10.5306/wjco.v11.i4.190

 
         
                         
                 
                 
                 
                 
                 
                         
                         
                        