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Outcomes in the Asian subgroup of the phase III randomised HIMALAYA study of tremelimumab plus durvalumab in unresectable hepatocellular carcinoma.
Lau, George; Abou-Alfa, Ghassan K; Cheng, Ann-Lii; Sukeepaisarnjaroen, Wattana; Dao, Tu Van; Kang, Yoon Koo; Thungappa, Satheesh Chiradoni; Kudo, Masatoshi; Sangro, Bruno; Kelley, Robin Kate; Furuse, Junji; Park, Joong-Won; Sunpaweravong, Patrapim; Fasolo, Angelica; Yau, Thomas; Kawaoka, Tomokazu; Azevedo, Sergio; Reig, Maria; Assenat, Eric; Yarchoan, Mark; He, Aiwu Ruth; Makowsky, Mallory; Gupta, Charu; Negro, Alejandra; Chan, Stephen L.
Afiliação
  • Lau G; Humanity and Health Clinical Trial Center, Humanity and Health Medical Group, Hong Kong Special Administrative Region, China.
  • Abou-Alfa GK; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA; Weill Medical College, Cornell University, New York, New York, USA. Electronic address: abou-alg@MSKCC.ORG.
  • Cheng AL; National Taiwan University Cancer Center, National Taiwan University Hospital, Taipei, Taiwan.
  • Sukeepaisarnjaroen W; Department of Medicine, Srinagarind Hospital, Khon Kaen University, Khon Kaen, Thailand.
  • Dao TV; Cancer Research and Clinical Trials Center, Department of Optimal Therapy, National Cancer Hospital, Hanoi, Vietnam.
  • Kang YK; Department of Oncology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea.
  • Thungappa SC; Sri Venkateshwara Hospital, Bangalore, India.
  • Kudo M; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan.
  • Sangro B; Liver Unit and HPB Oncology Area, Cancer Center Clínica Universidad de Navarra and CIBEREHD, Pamplona, Spain.
  • Kelley RK; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California, USA.
  • Furuse J; Department of Gastroenterology, Kanagawa Cancer Center, Yokohama, Japan.
  • Park JW; Department of Gastroenterology and Hepatology, Center for Liver and Pancreatobiliary Cancer, National Cancer Center, Goyang, Republic of Korea.
  • Sunpaweravong P; Department of Internal Medicine, Prince of Songkla University Hospital, Songkhla, Thailand.
  • Fasolo A; Fondazione Michelangelo, Milan, Italy.
  • Yau T; Queen Mary Hospital, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Kawaoka T; Department of Gastroenterology and Metabolism, Hiroshima University, Hiroshima, Japan.
  • Azevedo S; Department of Internal Medicine, UPCO-Hospital de Clínicas de Porto Alegre, Porto Alegre, Brasil.
  • Reig M; Barcelona Clinic Liver Cancer (BCLC), Liver Oncology Unit, Liver Unit, Hospital Clinic de Barcelona, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.
  • Assenat E; Department of Medical Oncology, Saint Eloi Hospital, Montpellier University, Montpellier, France.
  • Yarchoan M; Department of Oncology, Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.
  • He AR; Division of Hematology and Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, District of Columbia, USA.
  • Makowsky M; AstraZeneca, Gaithersburg, Maryland, USA.
  • Gupta C; AstraZeneca, Wilmington, Delaware, USA.
  • Negro A; AstraZeneca, Gaithersburg, Maryland, USA.
  • 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 Special Administrative Region, China.
J Hepatol ; 2024 Jul 30.
Article em En | MEDLINE | ID: mdl-39089633
ABSTRACT
BACKGROUND &

AIMS:

In the global, phase III HIMALAYA study in unresectable hepatocellular carcinoma (uHCC), STRIDE (Single Tremelimumab Regular Interval Durvalumab) improved overall survival (OS) vs. sorafenib; durvalumab was noninferior to sorafenib. HBV is the predominant HCC aetiology in most of Asia vs. HCV or nonviral aetiologies in Western countries and Japan. This analysis evaluated safety and efficacy outcomes for STRIDE and durvalumab monotherapy vs. sorafenib, in HIMALAYA participants enrolled in Asia, excluding Japan.

METHODS:

In HIMALAYA, participants were randomised to STRIDE, durvalumab, or sorafenib. The Asian subgroup in this analysis included participants enrolled in Hong Kong, India, South Korea, Taiwan, Thailand, and Vietnam. OS, objective response rate (ORR; per Response Evaluation Criteria in Solid Tumors, version 1.1), and safety were assessed in the Asian subgroup and in an exploratory subgroup of participants in Hong Kong and Taiwan.

RESULTS:

The Asian subgroup included 479 participants randomised to STRIDE (n=156), durvalumab (n=167), or sorafenib (n=156). OS was improved for STRIDE vs. sorafenib (HR 0.68; 95% CI 0.52-0.89]). The OS HR for durvalumab vs. sorafenib was 0.83 (95% CI 0.64-1.06). In Hong Kong and Taiwan (n=141), OS HRs for STRIDE vs. sorafenib and durvalumab vs. sorafenib were 0.44 (95% CI 0.26-0.77) and 0.64 (95% CI 0.37-1.08), respectively. In the Asian subgroup, ORR (including unconfirmed responses) was numerically higher for STRIDE (28.2%) and durvalumab (18.6%) vs. sorafenib (9.0%), and Grade 3/4 treatment-related adverse events were numerically lower for STRIDE (19.9%) and durvalumab (13.3%) vs. sorafenib (30.5%).

CONCLUSIONS:

STRIDE improved outcomes vs. sorafenib in the Asian subgroup. These results support the benefits of STRIDE for participants with uHCC globally, including the Asia-Pacific region. CLINICAL TRIAL NUMBER NCT03298451 IMPACT AND IMPLICATIONS The global, phase III HIMALAYA study found that the STRIDE (Single Tremelimumab Regular Interval Durvalumab) regimen improved overall survival (OS), including long-term OS, vs. sorafenib, and that durvalumab monotherapy was noninferior to sorafenib in participants with unresectable hepatocellular carcinoma (uHCC). However, there are differences in the aetiology and clinical practices related to HCC in parts of Asia, compared to Western countries and Japan, which could lead to differences in treatment outcomes between these regions. The results of this analysis demonstrate the benefits of STRIDE for participants in the Asia-Pacific region, consistent with the full, global study population. Overall, these findings continue to support the use of STRIDE in a diverse population, reflective of uHCC globally.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article