Evidence map›Paper›PMID 41585952›Full record

ArticleJHEP reports : innovation in hepatology2026

Pembrolizumab and stereotactic body radiotherapy combined in advanced hepatocellular carcinoma post sorafenib - A phase II trial (PEMRAD).

Grainne M O'Kane, Aruz Mesci, Raymond W Jang, Aisling Barry, Cynthia M Bocaya, Giselle M Boukhaled, Holly Acton, David Doddington, Rowena Rodrigo, Leo M L Chan and 13 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Review
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  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Grainne M O'KanePrincess Margaret Cancer Centre, Toronto, On, Canada.
Aruz MesciPrincess Margaret Cancer Centre, Toronto, On, Canada.
Raymond W JangPrincess Margaret Cancer Centre, Toronto, On, Canada.
Aisling BarryPrincess Margaret Cancer Centre, Toronto, On, Canada.
Cynthia M BocayaPrincess Margaret Cancer Centre, Toronto, On, Canada.
Giselle M BoukhaledPrincess Margaret Cancer Centre, Toronto, On, Canada.
Holly ActonPrincess Margaret Cancer Centre, Toronto, On, Canada.
David DoddingtonPrincess Margaret Cancer Centre, Toronto, On, Canada.
Rowena RodrigoPrincess Margaret Cancer Centre, Toronto, On, Canada.
Leo M L ChanPrincess Margaret Cancer Centre, Toronto, On, Canada.
Babak NoamaniPrincess Margaret Cancer Centre, Toronto, On, Canada.
Harry HarveyPrincess Margaret Cancer Centre, Toronto, On, Canada.
Andrew EliaPrincess Margaret Cancer Centre, Toronto, On, Canada.
Rhoda LawPrincess Margaret Cancer Centre, Toronto, On, Canada.
Rebecca PrincePrincess Margaret Cancer Centre, Toronto, On, Canada.
Mark DohertyPrincess Margaret Cancer Centre, Toronto, On, Canada.
Anna DoddPrincess Margaret Cancer Centre, Toronto, On, Canada.
David K WongPrincess Margaret Cancer Centre, Toronto, On, Canada.
Lisa WangPrincess Margaret Cancer Centre, Toronto, On, Canada.
Ben X WangPrincess Margaret Cancer Centre, Toronto, On, Canada.
Eric X ChenPrincess Margaret Cancer Centre, Toronto, On, Canada.
Laura A DawsonPrincess Margaret Cancer Centre, Toronto, On, Canada.
Jennifer J KnoxPrincess Margaret Cancer Centre, Toronto, On, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: There is strong rationale for integrated approaches combining immune checkpoint inhibitors with locoregional therapies in hepatocellular carcinoma (HCC). Methods: The PEMRAD phase II trial investigated pembrolizumab in combination with stereotactic body radiation therapy (SBRT) in patients with advanced HCC following progression on sorafenib. Patients received pembrolizumab on Day 1, and SBRT commenced on Day 2. Up to 10 hepatic lesions (<20 cm) were treated with SBRT. Pembrolizumab was continued every 21 days until disease progression, unacceptable toxicity, or withdrawal. The primary endpoint was objective response rate (ORR) by RECIST v1.1, with a hypothesized improvement to 40% for the combination. Tissue and liquid biopsies were collected for correlative analyses, including immunohistochemistry, longitudinal blood cytometry by time-of-flight, and serum cytokine assessment. Results: Between March 2018 and March 2023, 18 of a planned 22 patients were enrolled; 11 (61%) had macrovascular invasion (MVI) and 15 (83%) had extrahepatic metastases. Viral hepatitis was the underlying etiology in 50%. The ORR was 41% (95% CI 18-67%). Median progression-free survival was 5.4 months (2.8-9.9) and median overall survival was 12.6 months (5.7-25.8). Of 34 liver lesions treated with SBRT, only three progressed, in two patients. Among the 11 patients with MVI, 5 (45%) achieved a response, including one complete response. Treatment-related adverse events of grade ≥3 occurred in four patients (22%). One treatment-related death due to myocarditis was observed. Peripheral immunophenotyping showed that higher abundance of CD8 Conclusion: The combination of SBRT and pembrolizumab demonstrated a high response rate as second-line therapy for advanced HCC and warrants further evaluation, particularly in patients with MVI. Impact and implications: This study demonstrates that combining stereotactic body radiotherapy with pembrolizumab is feasible and yields promising response rates in patients with advanced, previously treated hepatocellular carcinoma, including those with macrovascular invasion - a group typically associated with poor outcomes. These findings support further evaluation of this integrated approach and provide important guidance for the design of future clinical trials aimed at improving outcomes in advanced hepatocellular carcinoma.

Indexed as

advanced HCCcombination treatmentPD-1 inhibitorsecond-lineStereotactic body radiotherapy

Identifiers

PMID41585952
PMCPMC12830293

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.