Toxicity compare
Adverse-event rates side by side across products of the same class. Any-grade and grade 3 or higher, from the US prescribing information where read. Blank means not sourced, not zero. Trial populations differ, so compare with care.
138 of 983 adverse-event rows
| Trial / note | ||||
|---|---|---|---|---|
Neutropenia | 91% | 82% | ECHELON-1, A+AVD arm · source | |
Neutropenia | 78% | 49% | ASCENT, Trodelvy arm, n=258 · source | |
Thrombocytopenia | — | 41% | ||
Neutropenia | — | 40% | ||
Neutropenia | — | 28.3% | ||
Neutropenia Febrile neutropenia | — | 27% | ||
Neutropenia Febrile neutropenia | 19% | 19% | ECHELON-1, A+AVD arm · source | |
Neutropenia | — | 18% | DESTINY-Breast03/04; all-grade rates ≥20% per label · source | |
Rash / skin Rash | 68% | 15% | EV-302 with pembrolizumab, n=440 · source | |
Hyperglycaemia Hyperglycaemia (grade 3-4 glucose elevation) | — | 14% | EV-302 with pembrolizumab, n=440 · source | |
Neutropenia Febrile neutropenia | — | 13.8% | ||
Diarrhoea | 59% | 11% | ASCENT, Trodelvy arm, n=258 · source | |
Peripheral neuropathy Peripheral sensory neuropathy | 65% | 10% | ECHELON-1, A+AVD arm · source | |
Anaemia | 94% | 9% | ASCENT, Trodelvy arm, n=258 · source | |
Peripheral neuropathy | 67% | 8% | EV-302 with pembrolizumab, n=440 · source | |
Anaemia | — | 7% | DESTINY-Breast03/04; all-grade rates ≥20% per label · source | |
Nausea | — | 7% | DESTINY-Breast03/04; all-grade rates ≥20% per label · source | |
Stomatitis | 59% | 7% | TROPION-Breast01, n=360 · source | |
Fatigue | 51% | 6% | EV-302 with pembrolizumab, n=440 · source | |
Fatigue | 65% | 6% | ASCENT, Trodelvy arm, n=258 · source | |
Fatigue | — | 6% | DESTINY-Breast03/04; all-grade rates ≥20% per label · source | |
Peripheral neuropathy | 38% | 6% | innovaTV 301, n=250 · source | |
Thrombocytopenia | 29% | 6% | KATHERINE (adjuvant) · source | |
Diarrhoea | 38% | 4.5% | EV-302 with pembrolizumab, n=440 · source | |
Fatigue | 44% | 4.2% | TROPION-Breast01, n=360 · source | |
Weight decrease | 33% | 3.6% | EV-302 with pembrolizumab, n=440 · source | |
Corneal complications | — | 3.2% | innovaTV 301, n=250 · source | |
Nausea | 57% | 3.1% | ASCENT, Trodelvy arm, n=258 · source | |
Vomiting | 33% | 3% | ECHELON-1, A+AVD arm · source | |
Constipation | 42% | 2% | ECHELON-1, A+AVD arm · source | |
Nausea | 40% | 2% | ECHELON-1, A+AVD arm · source | |
Decreased appetite | 33% | 1.8% | EV-302 with pembrolizumab, n=440 · source | |
Decreased appetite | 28% | 1.6% | ASCENT, Trodelvy arm, n=258 · source | |
Peripheral neuropathy | 52.9% | 1.6% | POLARIX Pola-R-CHP arm | |
Vomiting | 33% | 1.6% | ASCENT, Trodelvy arm, n=258 · source | |
Nausea | 56% | 1.4% | TROPION-Breast01, n=360 · source | |
Ocular Keratitis | 24% | 1.1% | TROPION-Breast01, n=360 · source | |
Pruritus | 41% | 1.1% | EV-302 with pembrolizumab, n=440 · source | |
Vomiting | 24% | 1.1% | TROPION-Breast01, n=360 · source | |
Ocular Dry eye | 27% | 0.8% | TROPION-Breast01, n=360 · source | |
Alopecia | 35% | 0.5% | EV-302 with pembrolizumab, n=440 · source | |
Constipation | 37% | 0.4% | ASCENT, Trodelvy arm, n=258 · source | |
Rash / skin Rash | 12% | 0.4% | ASCENT, Trodelvy arm, n=258 · source | |
Constipation | 34% | 0.3% | TROPION-Breast01, n=360 · source | |
Alopecia | 38% | 0% | TROPION-Breast01, n=360 · source | |
Alopecia | 47% | 0% | ASCENT, Trodelvy arm, n=258 · source | |
Ocular Dry eye | 24% | 0% | EV-302 with pembrolizumab, n=440 · source | |
Abdominal pain | 34% | — | MIRASOL; all-grade rates · source | |
Alopecia | — | — | ||
Alopecia | — | — | ||
Alopecia | 24% | — | innovaTV 301, n=250 · source | |
Alopecia | — | — | DESTINY-Breast03/04; all-grade rates ≥20% per label · source | |
Anaemia | — | — | ||
Anaemia | — | — | ||
Anaemia | — | — | ||
Anaemia | — | — | ||
Constipation | — | — | DESTINY-Breast03/04; all-grade rates ≥20% per label · source | |
Decreased appetite | — | — | ||
Decreased appetite | — | — | ||
Decreased appetite | — | — | ||
Decreased appetite | 24% | — | innovaTV 301, n=250 · source | |
Decreased appetite | — | — | DESTINY-Breast03/04; all-grade rates ≥20% per label · source | |
Diarrhoea | 29% | — | MIRASOL; all-grade rates · source | |
Diarrhoea | 30.8% | — | ||
Epistaxis | 26% | — | innovaTV 301, n=250 · source | |
Fatigue | — | — | ||
Fatigue | 47% | — | MIRASOL; all-grade rates · source | |
Fatigue | — | — | ||
Fatigue | — | — | ||
Fatigue | — | — | ||
Fatigue | — | — | ||
Fatigue | 28% | — | innovaTV 301, n=250 · source | |
Fatigue | 50% | — | KATHERINE (adjuvant) · source | |
Fatigue | — | — | ||
Haemorrhage | — | — | ||
Haemorrhage | 21% | — | innovaTV 301, n=250 · source | |
Haemorrhage | 29% | — | KATHERINE (adjuvant) · source | |
Headache | 28% | — | KATHERINE (adjuvant) · source | |
Hepatotoxicity AST/ALT increased | — | — | ||
Hepatotoxicity Hepatotoxicity including veno-occlusive disease | — | — | ||
Hepatotoxicity Hepatic veno-occlusive disease | 14% | — | Boxed warning; 22% of those who went on to transplant in INO-VATE · source | |
Hepatotoxicity Transaminase elevation | 27% | — | ||
Hepatotoxicity AST increased | 57% | — | MIRASOL; all-grade rates · source | |
Hepatotoxicity ALT increased | 38% | — | MIRASOL; all-grade rates · source | |
Hepatotoxicity Transaminases increased | 32% | — | KATHERINE (adjuvant) · source | |
ILD / pneumonitis ILD/pneumonitis | — | — | ||
ILD / pneumonitis ILD/pneumonitis | — | — | ||
ILD / pneumonitis Interstitial lung disease / pneumonitis | 12% | — | 0.9% fatal; pooled breast studies at 5.4 mg/kg · source | |
ILD / pneumonitis Interstitial lung disease | 4% | — | ||
Increased GGT | — | — | ||
Infections | — | — | ||
Infections Infection | — | — | ||
Infusion reactions | — | — | ||
Left ventricular dysfunction | 3% | — | KATHERINE (adjuvant) · source | |
Musculoskeletal pain | 30% | — | KATHERINE (adjuvant) · source | |
Nausea | — | — | ||
Nausea | 27% | — | MIRASOL; all-grade rates · source | |
Nausea | — | — | ||
Nausea | — | — | ||
Nausea | — | — | ||
Nausea | — | — | ||
Nausea | — | — | ||
Nausea | — | — | ||
Nausea | 33% | — | innovaTV 301, n=250 · source | |
Nausea | 42% | — | KATHERINE (adjuvant) · source | |
Nausea | 60% | — | ||
Neutropenia | — | — | ||
Neutropenia | — | — | ||
Neutropenia | — | — | ||
Neutropenia | — | — | ||
Neutropenia | — | — | ||
Neutropenia | — | — | ||
Neutropenia | — | — | Most common grade ≥3 event in OptiTROP-Breast01; rates per publication | |
Neutropenia | — | — | ||
Neutropenia | — | — | ||
Ocular Keratopathy | — | — | Ocular events in most patients; boxed warning | |
Ocular Blurred vision | — | — | ||
Ocular Dry eye | — | — | ||
Ocular Blurred vision | 45% | — | MIRASOL; all-grade rates · source | |
Ocular Keratopathy | 37% | — | MIRASOL; all-grade rates · source | |
Ocular Dry eye | 29% | — | MIRASOL; all-grade rates · source | |
Ocular Conjunctival disorders | 37% | — | innovaTV 301, n=250 · source | |
Ocular Dry eye | 21% | — | innovaTV 301, n=250 · source | |
Oedema and effusions | — | — | ||
Peripheral neuropathy | — | — | ||
Peripheral neuropathy | 37% | — | MIRASOL; all-grade rates · source | |
Peripheral neuropathy | — | — | ||
Peripheral neuropathy | 28% | — | KATHERINE (adjuvant) · source | |
Peripheral neuropathy | — | — | ||
Peripheral oedema | — | — | ||
Rash / skin Photosensitivity/rash | — | — | ||
Stomatitis | — | — | ||
Thrombocytopenia | — | — | ||
Thrombocytopenia | — | — | ||
Thrombocytopenia | — | — | ||
Thrombocytopenia | — | — | ||
Vomiting | — | — | ||
Vomiting | — | — | DESTINY-Breast03/04; all-grade rates ≥20% per label · source |