Randomized phase II placebo controlled study of codrituzumab in previously treated patients with advanced hepatocellular carcinoma
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).
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Patients with advanced stage HCC are more refractory to GPC3-targeted immunotherapies.
“patients with advanced stage HCC are more refractory to these treatments62,64,65,97,98.”
From Multi-omic analysis of hepatocellular carcinoma reveals aberrant cis-regulatory changes and dysregulated retrotransposons with prognostic potential (2025) · cites this paper as [98]
Cited by
Sorted by citations
Progress and challenges in glypican-3 targeting for hepatocellular carcinoma therapy
Couzinet, A., Suzuki, T., & Nakatsura, T. (2024) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2024.2416975 · Cited by 27 · see citing works
Cheng, C. C. Y., Cheung, M. F., Lee, A. Y., Wu, Q., Chow, S. H.-C., Ang, J. Y. J., Riquelme Medina, I., Lo, G., Wu, H., Yang, W., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-09154-w · Cited by 3 · see citing works
- 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)
- ORCID
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review