Comparison of Toxicity Data in Patients Who Received [177Lu]Lu-PSMA-617 Within EAP and VISION Trial
Any grade AE | Grade ≥ 3 AE | |||||
---|---|---|---|---|---|---|
Event | VISION (n = 529) | EAP (n = 117) | P | VISION (n = 529) | EAP (n = 117) | P |
Anemia* | 168 (32%) | 44 (42%) | 0.04 | 68 (13%) | 19 (18%) | 0.15 |
Thrombocytopenia† | 91 (17%) | 51 (49%) | <0.001 | 42 (8%) | 13 (13%) | 0.13 |
Neutropenia‡ | 45 (9%) | 32 (32%) | <0.001 | 18 (3%) | 3 (3%) | 0.85 |
Lymphopenia‡ | 75 (14%) | 65 (66%) | <0.001 | 41 (8%) | 34 (34%) | <0.001 |
Leukopenia† | 66 (12%) | 49 (47%) | <0.001 | 13 (2%) | 5 (5%) | 0.19 |
177Lu-PSMA-617 discontinuation due to AE | 63 (12%) | 15 (13%) | 0.78 | 37 (7%) | 7 (6%) | 0.69 |