Meeting enrollment targets in IMbrave152/SKYSCRAPER-14, a global phase 3 study in patients with unresectable hepatocellular carcinoma (HCC).
Abstract
1585 Background: The FDA has released guidance that the patient population in clinical studies should be representative of the intended-use population and the epidemiology of the disease, particularly in terms of race and ethnicity. IMbrave152/SKYSCRAPER-14 (NCT05904886) is a global phase 3 trial in patients with HCC, a disease with a globally high Asian and African prevalence, and which significantly impacts underrepresented (including Black and Hispanic) patients in the USA. Enrollment goals (by race/ethnicity), as well as operational and protocol-driven tactics to meet those goals, were implemented for IMbrave152. As of January 2, 2025, the targets for Black and Hispanic patients were met. Methods: Global recruitment began on September 14, 2023. Operational tactics included: feasibility questions about the ability to recruit underrepresented populations; utilization of internal and external databases to identify sites that could enroll underrepresented patients; incorporation of patient input; and enhanced patient-support services to facilitate recruitment and retention. Protocol-driven tactics included: modifying inclusion and exclusion criteria (considering race/ethnicity); streamlining study assessments; flexibility to use decentralized processes; and inclusion of an Africa Extension Cohort, which allowed for the recruitment of patients in Africa beyond the intent-to-treat population. Results: As of January 2, 2025, the randomized, global population included 8% Black and 14% Hispanic patients (US recruitment included 16% Black and 19% Hispanic patients), exceeding other global HCC studies, which recruited 2% or fewer Black patients and 11% or fewer Hispanic patients. Only two out of seven phase 3 studies in recent years have reported on Hispanic patient recruitment. Conclusions: IMbrave152 recruited the highest percentage of Black and Hispanic patients to date in a global phase 3 HCC study. These results demonstrate that recruitment of an underrepresented population is feasible if operational and protocol-driven tactics are utilized. Clinical trial information: NCT05904886 . Study White, % Asian, % Black, % Hispanic, % Global enrollment from Asia (excl. Japan), % IMbrave152 32.7 54.7 8.0 13.6 46.7 IMbrave150 1 34.9 56.7 2.0 NR 40.1 REFLECT 2 28.9 69.2 NR NR 67.1* HIMALAYA 3 44.5 50.9 1.6 4.7 40.9 LEAP-002 4 43.5 43.5 1.6 † 11.2 30.7 CheckMate-459 5 53.2 44.7 0.7 NR 25.3 RATIONALE-301 6 NR NR NR NR 63.1 COSMIC-312 7 50.9 31.4 1.7 NR 28.8 1 Finn et al. NEJM 2020; 2 Kudo et al. Lancet 2018; 3 Abou-Alfa et al. NEJM Evid 2022; 4 Llovet et al. Lancet 2023; 5 Yau et al. Lancet Oncol 2022; 6 Qin et al. JAMA Oncol 2023; 7 Kelley et al. Lancet Oncol 2022. NR, not reported. *Asia-Pacific region. † Multiple races, including 9 additional patients who were Black plus either Asian or White, were also reported.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (12)
Christopher Cotter
Genentech, Inc., South San Francisco, CA
Ruma Bhagat
Genentech, Inc., South San Francisco, CA
Huwaida Bulhan
Roche Kenya Limited, Nairobi, Kenya
Patty Leon
Genentech, Inc., South San Francisco, CA
Ya-Chen Lin
Genentech, a Member of the Roche Group, South San Francisco, CA
Nicole Richie
Renee Sims
Roche Products Limited, Welwyn Garden City, United Kingdom
Jessica Spahn
Genentech, Inc., South San Francisco, CA
Michael Stamatis
Genentech, Inc., South San Francisco, CA
Lisa Yalovsky
Roche Products Limited, Welwyn Garden City, United Kingdom
Huaqi Zhu
Roche China, Shanghai, China
Yasmin Ibrahim
Hepatitis B Foundation, Doylestown, PA