Back to Search Start Over

Three-Year Overall Survival with Tebentafusp in Metastatic Uveal Melanoma.

Authors :
Hassel JC
Piperno-Neumann S
Rutkowski P
Baurain JF
Schlaak M
Butler MO
Sullivan RJ
Dummer R
Kirkwood JM
Orloff M
Sacco JJ
Ochsenreither S
Joshua AM
Gastaud L
Curti B
Piulats JM
Salama AKS
Shoushtari AN
Demidov L
Milhem M
Chmielowski B
Kim KB
Carvajal RD
Hamid O
Collins L
Ranade K
Holland C
Pfeiffer C
Nathan P
Source :
The New England journal of medicine [N Engl J Med] 2023 Dec 14; Vol. 389 (24), pp. 2256-2266. Date of Electronic Publication: 2023 Oct 21.
Publication Year :
2023

Abstract

Background: Tebentafusp, a T-cell receptor-bispecific molecule that targets glycoprotein 100 and CD3, is approved for adult patients who are positive for HLA-A*02:01 and have unresectable or metastatic uveal melanoma. The primary analysis in the present phase 3 trial supported a long-term survival benefit associated with the drug.<br />Methods: We report the 3-year efficacy and safety results from our open-label, phase 3 trial in which HLA-A*02:01-positive patients with previously untreated metastatic uveal melanoma were randomly assigned in a 2:1 ratio to receive tebentafusp (tebentafusp group) or the investigator's choice of therapy with pembrolizumab, ipilimumab, or dacarbazine (control group), with randomization stratified according to the lactate dehydrogenase level. The primary end point was overall survival.<br />Results: At a minimum follow-up of 36 months, median overall survival was 21.6 months in the tebentafusp group and 16.9 months in the control group (hazard ratio for death, 0.68; 95% confidence interval, 0.54 to 0.87). The estimated percentage of patients surviving at 3 years was 27% in the tebentafusp group and 18% in the control group. The most common treatment-related adverse events of any grade in the tebentafusp group were rash (83%), pyrexia (76%), pruritus (70%), and hypotension (38%). Most tebentafusp-related adverse events occurred early during treatment, and no new adverse events were observed with long-term administration. The percentage of patients who discontinued treatment because of adverse events continued to be low in both treatment groups (2% in the tebentafusp group and 5% in the control group). No treatment-related deaths occurred.<br />Conclusions: This 3-year analysis supported a continued long-term benefit of tebentafusp for overall survival among adult HLA-A*02:01-positive patients with previously untreated metastatic uveal melanoma. (Funded by Immunocore; IMCgp100-202 ClinicalTrials.gov number, NCT03070392; EudraCT number, 2015-003153-18.).<br /> (Copyright © 2023 Massachusetts Medical Society.)

Details

Language :
English
ISSN :
1533-4406
Volume :
389
Issue :
24
Database :
MEDLINE
Journal :
The New England journal of medicine
Publication Type :
Academic Journal
Accession number :
37870955
Full Text :
https://doi.org/10.1056/NEJMoa2304753