Table 1.
Type | Drug | Mechanism of CIPN | Cumulative and Dose | Incidence of CIPN | Acute Neuropathy | Chronic Neuropathy | Additional Features |
---|---|---|---|---|---|---|---|
Platinum-Based | Cisplatin Carboplatin Oxaliplatin | Nuclear and mitochondrial DNA damage | Cisplatin >300 mg/m2, Oxalipatin >800 mg/m2 may be needed after the first dose | Cisplatin 49–100%, Carboplatin 13–42%, Oxaliplatin 85–95% | Cold-induced dysesthesias (hand/face), Muscle cramps | Sensory neuropathy/ neuronopathy, ataxia | “Coasting”, cranial nerve involvement: hearing loss, tinnitus, ageusia, Lhermitte’s phenomenon |
Taxanes | Docetaxel Paclitaxel Nab-paclitaxel Cabazitaxel Ixabepilone | Stabilization of microtubule polymers | Docetaxel ~400 mg/m2 Paclitaxel ~1000 mg/m2; doses of ≥250 mg/m2 may be needed after the first dose | 48.2% | Taste impairment | Sensorimotor neuropathy | Occasionally cranial nerves, mononeuropathies, autonomic features, “coasting” |
Vinca alkaloids | Vincristine Vinblastine Vinorelbine Vindesine | Destabilization of microtubule polymers | Vincristine >4 mg/m2 may be needed after the first dose | 20%; Vincristine 30–40% | Taste impairment | Sensorimotor neuropathy | Occasionally cranial nerves, mononeuropathies, autonomic features, possible ‘coasting’ |
Brentuximab vedotin | Brentuximab vedotin | Destabilization of microtubule polymers | 36–53% | Demyelinating, sensorimotor neuropathy | Autonomic myokymia | Conjugated antibody | |
Epothilones | Eribulin | Destabilization of microtubule polymers | 25% | NS | Sensorimotor neuropathy | Conjugated antibody | |
Ado-trastuzumab Emtansine | Ado-trastuzumab Emtansine | Destabilization of microtubule polymers | 13% after the first dose | NS | Sensorimotor neuropathy | Conjugated antibody | |
Proteasome inhibitor | Bortezomib Carfilzomib Ixazomib | Proteasome inhibitor | NS | Small fiber neuropathy, Severe polyradiculoneuropathy | Fewer CIPNs with subcutaneous delivery of bortezomib |
Abbreviations: NS, not specified.