Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 819

The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.

Tremelimumab in combination with ablation in patients with advanced hepatocellular carcinoma

Open access
Duffy, Austin G., Ulahannan, Susanna V., Makorova-Rusher, Oxana, Rahma, Osama, Wedemeyer, Heiner, Pratt, Drew, Davis, Jeremy L., Hughes, Marybeth S., Heller, Theo, ElGindi, Mei, Uppala, Ashish, Korangy, Firouzeh, Kleiner, David E., Figg, William D., Venzon, David, Steinberg, Seth M., Venkatesan, Aradhana M., Krishnasamy, Venkatesh, Abi-Jaoudeh, Nadine, Levy, Elliot, Wood, Brad J., Greten, Tim F.·2017·Journal of Hepatology

Abstract

Background & Aims Tremelimumab is a fully human monoclonal antibody that binds to cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) on the surface of activated T lymphocytes. Ablative therapies induce a peripheral immune response which may enhance the effect of anti-CTLA4 treatment in patients with advanced hepatocellular carcinoma (HCC). This study aimed to demonstrate whether tremelimumab could be combined safely and feasibly with ablation. Methods Thirty-two patients with HCC were enrolled: male:female: 28:4; median age: 62 (range 36–76). Patients were given tremelimumab at two dose levels (3.5 and 10 mg/kg i.v.) every 4 weeks for 6 doses, followed by 3-monthly infusions until off-treatment criteria were met. On day 36, patients underwent subtotal radiofrequency ablation or chemoablation. Staging was performed by contrast-enhanced CT or MRI scan every 8 weeks. Results No dose-limiting toxicities were encountered. The most common toxicity was pruritus. Of the 19 evaluable patients, five (26.3%; 95% CI: 9.1–51.2%) achieved a confirmed partial response. Twelve of 14 patients with quantifiable HCV experienced a marked reduction in viral load. Six-week tumor biopsies showed a clear increase in CD8+ T cells in patients showing a clinical benefit only. Six and 12-month probabilities of tumor progression free survival for this refractory HCC population were 57.1% and 33.1% respectively, with median time to tumor progression of 7.4 months (95% CI 4.7 to 19.4 months). Median overall survival was 12.3 months (95% CI 9.3 to 15.4 months). Conclusions Tremelimumab in combination with tumor ablation is a potential new treatment for patients with advanced HCC, and leads to the accumulation of intratumoral CD8+ T cells. Positive clinical activity was seen, with a possible surrogate reduction in HCV viral load. Lay summary Studies have shown that the killing of tumors by direct methods (known as ablation) can result in the immune system being activated or switched on. The immune system could potentially also recognize and kill the cancer that is left behind. There are new drugs available known as immune checkpoint inhibitors which could enhance this effect. Here, we test one of these drugs (tremelimumab) together with ablation.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.jhep.2016.10.029

Cites

25 of 25 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 25 references

Cited by

See all 819

Metadata

Authors
Duffy, A. G., Ulahannan, S. V., Makorova-Rusher, O., Rahma, O., Wedemeyer, H., Pratt, D., Davis, J. L., Hughes, M. S., Heller, T., ElGindi, M., Uppala, A., Korangy, F., Kleiner, D. E., Figg, W. D., Venzon, D., Steinberg, S. M., Venkatesan, A. M., Krishnasamy, V., Abi-Jaoudeh, N., Levy, E., Wood, B. J., & Greten, T. F.
Venue
Journal of Hepatology
Publisher
Elsevier BV
Published
2017-03
Volume
66
Issue
3
Pages
545-551
ISSN
0168-8278 (ISSN-L)
OpenAlex
W2546700240
Cited by
819
References
25
FWCI
35.01
Type
journal article
Language
en
Open access
green

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

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Tremelimumab in combination with ablation in patients with advanced hepatocellular carcinoma. https://app.cochat.ai/papers/10.1016/j.jhep.2016.10.029
The paper
Duffy, A. G., Ulahannan, S. V., Makorova-Rusher, O., Rahma, O., Wedemeyer, H., Pratt, D., Davis, J. L., Hughes, M. S., Heller, T., ElGindi, M., Uppala, A., Korangy, F., Kleiner, D. E., Figg, W. D., Venzon, D., Steinberg, S. M., Venkatesan, A. M., Krishnasamy, V., Abi-Jaoudeh, N., . . . Greten, T. F. (2017). Tremelimumab in combination with ablation in patients with advanced hepatocellular carcinoma. Journal of Hepatology. https://doi.org/10.1016/j.jhep.2016.10.029

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.