TY - JOUR
T1 - Four-year overall survival update from the phase III HIMALAYA study of tremelimumab plus durvalumab in unresectable hepatocellular carcinoma
AU - HIMALAYA investigators
AU - Sangro, B.
AU - Chan, S. L.
AU - Kelley, R. K.
AU - Lau, G.
AU - Kudo, M.
AU - Sukeepaisarnjaroen, W.
AU - Yarchoan, M.
AU - De Toni, E. N.
AU - Furuse, J.
AU - Kang, Y. K.
AU - Galle, P. R.
AU - Rimassa, L.
AU - Heurgué, A.
AU - Tam, V. C.
AU - Van Dao, T.
AU - Thungappa, S. C.
AU - Breder, V.
AU - Ostapenko, Y.
AU - Reig, M.
AU - Makowsky, M.
AU - Paskow, M. J.
AU - Gupta, C.
AU - Kurland, J. F.
AU - Negro, A.
AU - Abou-Alfa, G. K.
AU - Azevedo, Sergio
AU - Braghiroli, Maria Ignez
AU - Girotto, Gustavo
AU - Bragagnoli, Arinilda
AU - Branco, Ricardo
AU - Faccio, Adilson
AU - Moretto, Andrea
AU - Skare, Nils
AU - Dutra, Jamille
AU - Viola, Luciana
AU - Vianna, Karina
AU - Meton, Fernando
AU - Sette, Claudia
AU - Faulhaber, Amanda
AU - Tam, Vincent C.
AU - Couture, Felix
AU - Biagi, Jim
AU - Castel, Helene
AU - Mulder, Karen
AU - Ko, Yoo Joung
AU - Zbuk, Kevin
AU - Welch, Stephen
AU - Beaudoin, Annie
AU - Heurgué, Alexandra
AU - Sirachainan, Ekaphop
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/5
Y1 - 2024/5
N2 - Background: In the phase III HIMALAYA study (NCT03298451) in unresectable hepatocellular carcinoma (uHCC), STRIDE (Single Tremelimumab Regular Interval Durvalumab) significantly improved overall survival (OS) versus sorafenib; durvalumab monotherapy was noninferior to sorafenib for OS. Results reported herein are from a 4-year updated OS analysis of HIMALAYA. Patients and methods: Participants with uHCC and no previous systemic treatment were randomized to STRIDE (n = 393), durvalumab (n = 389), or sorafenib (n = 389). The updated data cut-off was 23 January 2023. OS and serious adverse events (AEs) were assessed. Additionally, baseline characteristics and subsequent therapies were analyzed in long-term survivors (≥36 months beyond randomization). Results: For STRIDE, durvalumab, and sorafenib, median [95% confidence interval (CI)] follow-up was 49.12 months (46.95-50.17 months), 48.46 months (46.82-49.81 months), and 47.31 months (45.08-49.15 months), respectively. OS hazard ratio (95% CI) for STRIDE versus sorafenib was 0.78 (0.67-0.92). The 36-month OS rate for STRIDE was 30.7% versus 19.8% for sorafenib. The 48-month OS rate remained higher for STRIDE at 25.2%, versus 15.1% for sorafenib. The long-term OS benefit of STRIDE was observed across clinically relevant subgroups and was further improved in participants who achieved disease control. Long-term survivors with STRIDE (n = 103) included participants across clinically relevant subgroups, and 57.3% (59/103) had no reported subsequent anticancer therapy. No new serious treatment-related AEs occurred with STRIDE from the primary analysis (17.5%; 68/388). Durvalumab maintained OS noninferiority to sorafenib and no late-onset safety signals were identified. Conclusions: These data represent the longest follow-up to date in phase III studies in uHCC. The unprecedented 3- and 4-year OS rates reinforce the sustained long-term OS benefit of STRIDE versus sorafenib. STRIDE maintained a tolerable yet differentiated safety profile from other current uHCC therapies. Results continue to support the long-term benefits of STRIDE in a diverse population, reflective of uHCC globally.
AB - Background: In the phase III HIMALAYA study (NCT03298451) in unresectable hepatocellular carcinoma (uHCC), STRIDE (Single Tremelimumab Regular Interval Durvalumab) significantly improved overall survival (OS) versus sorafenib; durvalumab monotherapy was noninferior to sorafenib for OS. Results reported herein are from a 4-year updated OS analysis of HIMALAYA. Patients and methods: Participants with uHCC and no previous systemic treatment were randomized to STRIDE (n = 393), durvalumab (n = 389), or sorafenib (n = 389). The updated data cut-off was 23 January 2023. OS and serious adverse events (AEs) were assessed. Additionally, baseline characteristics and subsequent therapies were analyzed in long-term survivors (≥36 months beyond randomization). Results: For STRIDE, durvalumab, and sorafenib, median [95% confidence interval (CI)] follow-up was 49.12 months (46.95-50.17 months), 48.46 months (46.82-49.81 months), and 47.31 months (45.08-49.15 months), respectively. OS hazard ratio (95% CI) for STRIDE versus sorafenib was 0.78 (0.67-0.92). The 36-month OS rate for STRIDE was 30.7% versus 19.8% for sorafenib. The 48-month OS rate remained higher for STRIDE at 25.2%, versus 15.1% for sorafenib. The long-term OS benefit of STRIDE was observed across clinically relevant subgroups and was further improved in participants who achieved disease control. Long-term survivors with STRIDE (n = 103) included participants across clinically relevant subgroups, and 57.3% (59/103) had no reported subsequent anticancer therapy. No new serious treatment-related AEs occurred with STRIDE from the primary analysis (17.5%; 68/388). Durvalumab maintained OS noninferiority to sorafenib and no late-onset safety signals were identified. Conclusions: These data represent the longest follow-up to date in phase III studies in uHCC. The unprecedented 3- and 4-year OS rates reinforce the sustained long-term OS benefit of STRIDE versus sorafenib. STRIDE maintained a tolerable yet differentiated safety profile from other current uHCC therapies. Results continue to support the long-term benefits of STRIDE in a diverse population, reflective of uHCC globally.
KW - durvalumab
KW - immune checkpoint inhibitor
KW - overall survival
KW - tremelimumab
KW - unresectable hepatocellular carcinoma
UR - https://www.scopus.com/pages/publications/85188011236
U2 - 10.1016/j.annonc.2024.02.005
DO - 10.1016/j.annonc.2024.02.005
M3 - Article
C2 - 38382875
AN - SCOPUS:85188011236
SN - 0923-7534
VL - 35
SP - 448
EP - 457
JO - Annals of Oncology
JF - Annals of Oncology
IS - 5
ER -