Evidence map›Paper›PMID 41951273›Full record

ArticleJHEP reports : innovation in hepatology2026

Radiation-induced lymphopenia is associated with survival in patients with hepatocellular carcinoma treated with stereotactic body radiotherapy.

Landon L Chan, Vanessa T Y Yeung, Winnie M T Soo, Darren M C Poon, Macy Tong, Daisy C M Lam, Virginia H Y Kwong, Eric K H Chan, Aaron Y H Ip, Michael L M Cheung and 6 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Landon L ChanDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong; State Key Laboratory of Translational Oncology, Sir YK Pao Centre for Cancer, Hong Kong Cancer Institute, The Chinese University of Hong Kong, Hong Kong.
Vanessa T Y YeungDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Winnie M T SooDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Darren M C PoonDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Macy TongDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Daisy C M LamDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Virginia H Y KwongDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Eric K H ChanDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Aaron Y H IpDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Michael L M CheungDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Felix F Y ShumDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
David R JohnsonDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Benjamin H W LamDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Wesley K Y WongDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Florence S T MokDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Stephen L ChanDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong; State Key Laboratory of Translational Oncology, Sir YK Pao Centre for Cancer, Hong Kong Cancer Institute, The Chinese University of Hong Kong, Hong Kong. Electronic address: chanlam_stephen@cuhk.edu.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsStereotactic body radiotherapy (SBRT) is increasingly used in the treatment of hepatocellular carcinoma (HCC). Severe radiation-induced lymphopenia (RIL) occurs in 30% to 40% of patients undergoing conventional fractionated radiotherapy and is associated with worse survival. However, the incidence of RIL and its effect on survival in patients with HCC treated with SBRT remain unclear.

methodsThis is a retrospective study of patients with HCC treated with SBRT in a tertiary cancer center in Hong Kong between January 2013 to December 2023. Patient and tumor characteristics were reviewed. Pre- and post-SBRT lymphocyte counts were collected. Severe RIL is defined as an absolute lymphocyte count <0.5x10

resultsA total of 147 patients were included. Most patients had BCLC stage 0/A disease (64.5%), and the median tumor size was 2.6 cm (range, 0.5-11.4 cm). Severe RIL was observed in 17 (13.5%) patients following SBRT. Severe RIL was associated with shorter median progression-free survival (8.0 vs. 9.9 months; p = 0.029) and overall survival (18.5 vs. 33.0 months; p <0.001). Larger low-dose irradiated liver volumes were associated with severe RIL (per 10-cc increase in V5: odds ratio [OR], 1.02; p = 0.04; per 10-cc increase in V10: OR, 1.03; p = 0.03), as was the presence of portal hypertension (OR, 3.68; p = 0.03).

conclusionsDevelopment of severe RIL in patients with HCC after SBRT is associated with poor survival. Minimizing low-dose radiation exposure to the liver is essential to reduce the risk of severe RIL. IMPACT AND IMPLICATIONS: Radiotherapy is an effective treatment for hepatocellular carcinoma (HCC) and is increasingly utilized across all disease stages. Radiation-induced lymphopenia (RIL) is associated with poor survival in many cancers but remains underexplored in HCC. The advent of stereotactic body radiotherapy enables highly precise radiation delivery, reducing toxicity, including RIL. In this study, we demonstrated that the incidence of severe RIL occurred significantly less frequently with stereotactic body radiotherapy than conventional fractionated radiotherapy in patients with HCC. We confirmed RIL as an independent predictor of inferior survival. We identified patients with portal hypertension, and those receiving larger low-dose liver irradiation volumes were at significantly higher risk of developing RIL. These results may guide clinicians in optimizing patient selection for radiotherapy and support the preferential use of advanced planning techniques in high-risk individuals to minimize RIL, potentially improving clinical outcomes.

Indexed as

hepatocellular carcinomaLymphopeniaprognosisstereotactic body radiotherapy

Identifiers

PMID41951273
PMCPMC12972977

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.