Evidence map›Paper›PMID 41749933›Full record

ArticleCancers2026

Toxicity of Ablative Radiation Therapy in the Management of Patients with Child-Pugh B/C Liver Function and Unresectable Hepatocellular Carcinoma (HCC).

William Sperduto, Taofik Oyekunle, Donna Niedzwiecki, Christine E Eyler, Brian Czito, Christopher G Willett, Devon Godfrey, Joseph K Salama, Manisha Palta, Sarah J Stephens

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

William SperdutoDepartment of Radiation Oncology, Mayo Clinic, Phoenix, AZ 85054, USA.
Taofik OyekunleDepartment of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, NC 27710, USA.
Donna NiedzwieckiDepartment of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, NC 27710, USA.
Christine E EylerDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Brian CzitoDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Christopher G WillettDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Devon GodfreyDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0001-6406-1126
Joseph K SalamaDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Manisha PaltaDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Sarah J StephensDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0002-1226-2329

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesHypofractionated ablative radiation is an increasingly popular option for patients with hepatocellular carcinoma (HCC). However, concern remains about the risk for radiation-induced liver toxicity in patients with decompensated liver function.

methodsWe retrospectively identified patients with underlying Child-Pugh (CP) B or C liver function treated at our University and Veterans Affairs (VA) departments from 2014 to 2019. Primary endpoints included treatment-related toxicity and dosimetric parameters.

results38 patients were included in the analysis. Most patients (98%) had CP B or Albumin-Bilirubin (ALBI) grade 2-3 (100%) liver disease. The median dose was 50 Gy (range 30-50) delivered in 5 or 10 fractions. Most patients had a single tumor treated (66%) with a median size of 3.1 cm (Interquartile Range (IQR) 2.3-4.1). The mean liver dose was 9.28 Gy (IQR 6.76-13.64) with a liver D800cc of 3.99 Gy (IQR 1.41-8.02). All patients completed their intended course with a median follow-up of 43 months. Four patients (10.3%) developed non-classical radiation-induced liver disease (RILD), comparable to the rate for patients with CP A function treated contemporaneously (8.3%). Otherwise, one patient (2.6%) experienced acute grade 3+ (non-RILD) hepatobiliary toxicity, while one patient (2.6%) experienced late grade 3+ hepatobiliary toxicity. Local control was promising with 2-year freedom from progression

conclusionsAblative radiation for patients with decompensated liver function and HCC appears well tolerated with low rates of RILD and encouraging local control. With careful selection, these patients should be considered for inclusion in future randomized trials.

Indexed as

Child-PughHCChepatocellular carcinomaradiation-induced liver dysfunctionRILDSBRTstereotactic body radiotherapy

Identifiers

PMID41749933
PMCPMC12939832

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.