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Uveal melanoma is a disease different from skin melanoma.
Tebentafusp is a bispecific protein that is formed by the fusion of an affinity-enhanced T cell receptor and an anti-CD3 effector, which can redirect T cells to target glycoprotein 100-positive cells
Tebentafusp is a bispecific protein that is formed by the fusion of an affinity-enhanced T cell receptor and an anti-CD3 effector, which can redirect T cells to target glycoprotein 100-positive cells
This study is an open-label phase 3 clinical trial that recruited HLA-A*02:01-positive patients with metastatic uveal melanoma who had not been treated before.
Overall survival of the intention-to-treat population
A total of 378 patients were randomly divided into two groups: 252 in the Tebentafusp group and 126 in the control group
The 1-year overall survival rates of the Tebentafusp group and the control group were 73% and 59%, respectively.
Progression-free survival in the intention-to-treat population
The most common treatment-related adverse events in the Tebentafusp group were cytokine-mediated events (due to T cell activation) and skin-related events (due to glycoprotein 100-positive melanocytes), including skin rash (83%), fever (76%) and itching (69%)
Changes in the incidence of treatment-related adverse events
All in all, compared with the control treatment, Tebentafusp treatment prolonged the overall survival of previously untreated patients with metastatic uveal melanoma
Compared with the control treatment, Tebentafusp treatment prolonged the overall survival of previously untreated patients with metastatic uveal melanoma
Original source:
Paul Nathan, et al.
Overall Survival Benefit with Tebentafusp in Metastatic Uveal Melanoma
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