Patterns of radiological progression in participants (pts) with embolization-eligible hepatocellular carcinoma (HCC) treated with durvalumab (D) + bevacizumab (B) + transarterial chemoembolization (TACE) and placebos + TACE: EMERALD-1 post hoc analysis.

B Bruno Sangro M Mohamed Bouattour (Medical Oncology, AP-HP Hôpital Beaujon, Paris, France) J Joong-Won Park (National Cancer Center and Myongji Hospital, Goyang, South Korea) D Dr. Consuelo Diaz (Instituto Nacional de Cancerología, Mexico City, Mexico) J Joseph P. Erinjeri (Interventional Radiology Service, Memorial Sloan Kettering Cancer Center, New York, NY) G Gustavo Vasconcelos Alves (Centro Integrado de Pesquisa em Oncologia, Hospital Nossa Senhora de Conceição, Porto Alegre, Brazil) S Shan-Zhi Gu (Department of Interventional Radiology, Hunan Cancer Hospital, Changsha, China) A Aleksei Manikhas (Oncology Department, City Clinical Oncological Dispensary, St. Petersburg, Russian Federation) H Hidekatsu Kuroda T Thatthan Suksombooncharoen (Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand) T Truc Hoi Trung Vo (Liver Tumor Department, Cho Ray Hospital, Ho Chi Minh City, Viet Nam) V Vikas S. Ostwal (Department of Medical Oncology, Tata Memorial Hospital, Mumbai, India) M Melissa A. Eastgate (School of Medicine, University of Queensland and Department of Medical Oncology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia) G Gina M. Vaccaro (Tennessee Oncology, Nashville, TN) R Rebecca Griffin (Oncology Biometrics, Late Oncology Statistics, AstraZeneca, Cambridge, United Kingdom) S Sajid Ali K Kavitha Balaji (Global Medical Affairs, AstraZeneca, Gaithersburg, MD) S Stephen Lam Chan

Abstract

574 Background: EMERALD-1 (NCT03778957) met its primary endpoint, demonstrating improved progression-free survival (PFS) in pts with locoregional HCC treated with D + B + TACE versus placebos (PBO) + TACE (stratified Cox proportional hazards hazard ratio [HR], 0.77; 95% confidence interval [CI], 0.61–0.98 [Lencioni R, et al. J Clin Oncol 2024;42(suppl 3). Abs LBA432]). This post hoc analysis assessed outcomes by radiological progression pattern in pts treated with D + B + TACE or PBO + TACE. Methods: Pts included in this analysis received D (1500 mg) or PBO for D (Q4W) in combination with conventional (c)- or drug-eluting bead (DEB)-TACE (investigator choice, 1–4 TACE procedures within 16 weeks). Subsequently, pts received D (1120 mg) + B (15 mg/kg), or PBO for D + B (Q3W). This study analyzed radiological progression patterns at the time of first progressive disease (PD) as assessed by the investigator per modified Response Evaluation Criteria in Solid Tumors. A new lesion was classified as a new intrahepatic lesion (NIH) or new extrahepatic lesion (NEH); tumor growth of existing intrahepatic lesions (increase of ≥20% of an existing target lesion with at least >5 mm absolute increase or unequivocal PD with a non-target lesion) was classified as intrahepatic growth (IHG; categories were not mutually exclusive). Efficacy was assessed by time to progression (TTP). Results: In the D + B + TACE arm, 53.9% of pts had PD, and in the PBO + TACE arm 79.0% of pts had PD. The most common pattern of disease progression across both treatment arms was NIH, occurring in 73 (35.8%) and 107 (52.2%) pts in the D + B + TACE and PBO + TACE arms, respectively, with 31 (15.2%) and 34 (16.6%) pts exhibiting IHG, and 24 (11.8%) and 39 (19.0%) pts exhibiting NEH, respectively. Improved TTP was observed in pts treated with D + B + TACE versus PBO + TACE, regardless of progression pattern (Table). Conclusions: Overall, the rate of progression was lower with D + B + TACE compared with PBO + TACE. The pattern of disease progression observed with D + B + TACE and PBO + TACE was similar, with NIH the most common pattern of progression in both treatment arms. Consistent benefit in TTP was observed with D + B + TACE versus PBO + TACE, regardless of progression pattern. Clinical trial information: NCT03778957 . NIH IHG NEH D + B + TACE (n=73) PBO + TACE (n=107) D + B + TACE (n=31) PBO + TACE (n=34) D + B + TACE (n=24) PBO + TACE (n=39) Median (95% CI) TTP, months 13.7 (10.8–16.5) 8.8 (7.0–10.9) 5.1 (3.0–9.0) 4.3 (2.9–4.8) 6.7 (2.8–16.6) 4.6 (2.9–6.8) HR (95% CI)* 0.78 (0.57–1.07) 0.61 (0.36–1.03) 0.66 (0.36–1.15) *HR and CI were estimated using a Cox proportional hazards model, the CI was calculated using a profile likelihood approach.

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 574-574
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

B

Bruno Sangro

M

Mohamed Bouattour

Medical Oncology, AP-HP Hôpital Beaujon, Paris, France

J

Joong-Won Park

National Cancer Center and Myongji Hospital, Goyang, South Korea

D

Dr. Consuelo Diaz

Instituto Nacional de Cancerología, Mexico City, Mexico

J

Joseph P. Erinjeri

Interventional Radiology Service, Memorial Sloan Kettering Cancer Center, New York, NY

G

Gustavo Vasconcelos Alves

Centro Integrado de Pesquisa em Oncologia, Hospital Nossa Senhora de Conceição, Porto Alegre, Brazil

S

Shan-Zhi Gu

Department of Interventional Radiology, Hunan Cancer Hospital, Changsha, China

A

Aleksei Manikhas

Oncology Department, City Clinical Oncological Dispensary, St. Petersburg, Russian Federation

H

Hidekatsu Kuroda

T

Thatthan Suksombooncharoen

Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand

T

Truc Hoi Trung Vo

Liver Tumor Department, Cho Ray Hospital, Ho Chi Minh City, Viet Nam

V

Vikas S. Ostwal

Department of Medical Oncology, Tata Memorial Hospital, Mumbai, India

M

Melissa A. Eastgate

School of Medicine, University of Queensland and Department of Medical Oncology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia

G

Gina M. Vaccaro

Tennessee Oncology, Nashville, TN

R

Rebecca Griffin

Oncology Biometrics, Late Oncology Statistics, AstraZeneca, Cambridge, United Kingdom

S

Sajid Ali

K

Kavitha Balaji

Global Medical Affairs, AstraZeneca, Gaithersburg, MD

S

Stephen Lam Chan