Cited by 137Hepatocellular Carcinoma Treatment and PrognosisColorectal Cancer Treatments and StudiesHepatitis B Virus Studies

Randomized phase II placebo controlled study of codrituzumab in previously treated patients with advanced hepatocellular carcinoma

Abou-Alfa, Ghassan K., Puig, Oscar, Daniele, Bruno, Kudo, Masatoshi, Merle, Philippe, Park, Joong-Won, Ross, Paul, Peron, Jean-Marie +21 more·2016·Journal of Hepatology

Abstract

Background & aims Codrituzumab, a humanized monoclonal antibody against Glypican-3 (GPC3) that is expressed in hepatocellular carcinoma (HCC), interacts with CD16/FcγRIIIa and triggers antibody-dependent cytotoxicity. Codrituzumab was studied vs. placebo in a randomized phase II trial in advanced HCC patients who had failed prior systemic therapy. Methods Patients with advanced HCC who had failed prior systemic therapy, ⩾18years, Eastern cooperative oncology group (ECOG) 0-1, Child-Pugh A were randomized 2:1 to biweekly codrituzumab 1600mg vs. placebo. Patients were stratified based on GPC3 immunohistochemical expression: 2+/3+, 1+, and 0. Primary endpoint was progression free survival. Secondary endpoints include overall survival (OS), tolerability, pharmacokinetics, and an exploratory endpoint in biomarkers analysis. Results 185 patients were enrolled: 125 received codrituzumab and 60 placebo: Median age 64/63, 85/75% male, 46/42% Asian, ECOG 0 65/63%, 74/77% having vascular invasion and/or extra-hepatic metastasis. 84%/70% had prior sorafenib. Drug exposure was 98.4% of planned dose, with an identical adverse events profile between the 2 groups. The median progression free survival and overall survival in the codrituzumab vs. placebo groups in months were: 2.6 vs. 1.5 (hazard ratios 0.97, p=0.87), and 8.7 vs. 10 (hazard ratios 0.96, p=0.82). Projected Ctrough at cycle 3day 1 based exposure, high CD16/FcγRIIIa on peripheral immune cells, and GPC3 expression in the tumor, were all associated with prolonged progression free survival and overall survival. Conclusions Codrituzumab did not show clinical benefit in this previously treated HCC population. Whether higher codrituzumab drug exposure or the use of CD16 and GPC3 as potential biomarkers would improve outcome remain unanswered questions. Lay summary Codrituzumab is a manufactured antibody against a liver cancer protein called glypican-3. In this clinical trial, codrituzumab was not found be effective against liver cancer. It was suggested though that a higher dose of codrituzumab or selecting patients with high level of glypican-3 or its mediator CD16 might improve outcome. Clinical trial registration This trial is registered at Clinicaltrials.gov (NCT01507168).

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Crossref · 10.1016/j.jhep.2016.04.004

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Authors
Abou-Alfa, G. K., Puig, O., Daniele, B., Kudo, M., Merle, P., Park, J.-W., Ross, P., Peron, J.-M., Ebert, O., Chan, S., Poon, T. P., Colombo, M., Okusaka, T., Ryoo, B.-Y., Minguez, B., Tanaka, T., Ohtomo, T., Ukrainskyj, S., Boisserie, F., Rutman, O., Chen, Y.-C., Xu, C., Shochat, E., Jukofsky, L., Reis, B., Chen, G., Di Laurenzio, L., Lee, R., & Yen, C.-J.
Affiliations
  • Azienda Ospedaliera G.Rummo (IT)
  • Kindai University Hospital (JP)
  • Hôpital de la Croix-Rousse (FR)
  • National Cancer Center (KR)
  • King's College Hospital (GB)
  • TUM Klinikum (DE)
  • Prince of Wales Hospital (CN)
  • Queen Mary Hospital (CN)
  • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (IT)
  • National Cancer Center Hospital (JP)
  • Asan Medical Center (KR)
  • Chugai Pharmaceutical Co., Ltd. (Japan) (JP)
  • F. Hoffmann-La Roche AG (CH)
  • National Cheng Kung University Hospital (TW)
Venue
Journal of Hepatology
Publisher
Elsevier BV
Published
2016-08
Volume
65
Issue
2
Pages
289-295
ISSN
0168-8278 (ISSN-L)
OpenAlex
W2341498785
Cited by
137
References
0
Citations by year
2026: 15 · 2025: 16 · 2024: 11 · 2023: 9 · 2022: 10 · 2021: 16 · 2020: 18 · 2019: 11 · 2018: 12 · 2017: 16 · 2016: 3
FWCI
10.07
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Hepatology (publishedVersion)
  • PubMed (publishedVersion)
  • The HKU Scholars Hub (University of Hong Kong) (submittedVersion)
  • mediaTUM (Technical University of Munich) (submittedVersion)
Topics
  • Health Sciences › Medicine › Hepatology › Hepatocellular Carcinoma Treatment and Prognosis
  • Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
  • Health Sciences › Medicine › Epidemiology › Hepatitis B Virus Studies
Keywords
hepatocellular carcinoma, glypican-3, monoclonal antibodies, antibody-dependent cellular cytotoxicity, progression-free survival, overall survival, biomarkers, drug exposure, previously treated patients, pharmacokinetics, adverse events
MeSH terms
Double-Blind Method, Female, Carcinoma, Hepatocellular, Humans, Liver Neoplasms, Male, Middle Aged, Treatment Outcome, Disease-Free Survival, Glypicans, Antibodies, Monoclonal, Humanized

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