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Four-year overall survival update from the phase III HIMALAYA study of tremelimumab plus durvalumab in unresectable hepatocellular carcinoma.
Sangro, B; Chan, S L; Kelley, R K; Lau, G; Kudo, M; Sukeepaisarnjaroen, W; Yarchoan, M; De Toni, E N; Furuse, J; Kang, Y K; Galle, P R; Rimassa, L; Heurgué, A; Tam, V C; Van Dao, T; Thungappa, S C; Breder, V; Ostapenko, Y; Reig, M; Makowsky, M; Paskow, M J; Gupta, C; Kurland, J F; Negro, A; Abou-Alfa, G K.
Afiliación
  • Sangro B; Liver Unit and HPB Oncology Area, Clínica Universidad de Navarra and CIBEREHD, Pamplona, Spain. Electronic address: bsangro@unav.es.
  • Chan SL; State Key Laboratory of Translational Oncology, Department of Clinical Oncology, Sir Yue-Kong Pao Center for Cancer, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Kelley RK; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, USA.
  • Lau G; Humanity and Health Clinical Trial Center, Humanity and Health Medical Group, Hong Kong SAR, China.
  • Kudo M; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan.
  • Sukeepaisarnjaroen W; Department of Medicine, Songklanagarind Hospital, Khon Kaen University, Khon Kaen, Thailand.
  • Yarchoan M; Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins, Baltimore, USA.
  • De Toni EN; Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.
  • Furuse J; Kanagawa Cancer Center, Yokohama, Japan.
  • Kang YK; Department of Oncology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea.
  • Galle PR; Department of Internal Medicine I, University Medical Center, Mainz, Germany.
  • Rimassa L; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan; Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
  • Heurgué A; Department of Hepato-Gastroenterology, Robert-Debré Hospital, Reims, France.
  • Tam VC; Tom Baker Cancer Centre, Department of Oncology, University of Calgary, Calgary, Canada.
  • Van Dao T; Cancer Research and Clinical Trials Center, Department of Optimal Therapy, National Cancer Hospital, Hanoi, Vietnam.
  • Thungappa SC; Health Care Global Enterprises Ltd, Bangalore, India.
  • Breder V; N. N. Blokhin Russian Cancer Research Center, Chemotherapy Unit, Moscow, Russia.
  • Ostapenko Y; Department of Minimally Invasive and Endoscopic Surgery, Interventional Radiology, National Cancer Institute, Kyiv, Ukraine.
  • Reig M; Barcelona Clinic Liver Cancer (BCLC), Liver Unit, Hospital Clinic de Barcelona, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.
  • Makowsky M; Oncology R&D, Late-Stage Development, AstraZeneca, Gaithersburg.
  • Paskow MJ; Global Medical Affairs, AstraZeneca, Gaithersburg.
  • Gupta C; Oncology Biometrics, Late Oncology Statistics, AstraZeneca, Wilmington.
  • Kurland JF; Oncology R&D, Late-Stage Development, AstraZeneca, Gaithersburg.
  • Negro A; Oncology R&D, Late-Stage Development, AstraZeneca, Gaithersburg.
  • Abou-Alfa GK; Department of Medicine, Memorial Sloan Kettering Cancer Center, Cornell University, New York; Weill Medical College, Cornell University, New York, USA; Trinity College Dublin, Dublin, Ireland.
Ann Oncol ; 35(5): 448-457, 2024 May.
Article en En | MEDLINE | ID: mdl-38382875
ABSTRACT

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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Hepatocelular / Anticuerpos Monoclonales Humanizados / Neoplasias Hepáticas / Anticuerpos Monoclonales Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Hepatocelular / Anticuerpos Monoclonales Humanizados / Neoplasias Hepáticas / Anticuerpos Monoclonales Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article