Evidence map›Paper›PMID 41413036›Full record

Trial reportNature communications2025

Stereotactic body radiotherapy with sintilimab and bevacizumab biosimilar in anti-PD-1 refractory hepatocellular carcinoma: the ReUNION-1 phase 2 trial.

Jing Tang, Yongqiang Yang, Dongen Liu, Bicheng Wang, Zhenyu Lin, Zilong Wu, Jinfeng Zhang, Dejun Zhang, Yaqin Liu, Minghui Ge and 4 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

14 authors.

Jing Tang *Cancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0000-0003-1013-147X
Yongqiang Yang *Cancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0009-0007-0043-6073
Dongen Liu *Cancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0009-0000-9019-765X
Bicheng Wang *Cancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0000-0002-4598-7721
Zhenyu LinCancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zilong WuCancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Jinfeng ZhangCancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Dejun ZhangCancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yaqin LiuThe State Key Laboratory of Neurology and Oncology Drug Development, Jiangsu Simcere Diagnostics Co., Ltd., Nanjing Simcere Medical Laboratory Science Co. Ltd, Nanjing, China.
Minghui GeThe State Key Laboratory of Neurology and Oncology Drug Development, Jiangsu Simcere Diagnostics Co., Ltd., Nanjing Simcere Medical Laboratory Science Co. Ltd, Nanjing, China.
Lei ChenThe International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Naval Medical University, Shanghai, China.ORCID http://orcid.org/0000-0002-9380-9559
Gang WuCancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. xhzlwg@163.com.ORCID http://orcid.org/0000-0001-6558-3508
Tao ZhangCancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. taozhangxh@hust.edu.cn.ORCID http://orcid.org/0000-0003-4018-3393
Jun XueCancer Centre, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. junxue_xh@hust.edu.cn.ORCID http://orcid.org/0000-0001-7323-0331

Funding

Chinese Society of Clinical Oncology (Chinese Society of Clinical Oncology, Beijing Xisike Clinical Oncology Research Foundation) Y-HS202102-0152National Natural Science Foundation of China (National Science Foundation of China) 82172977National Natural Science Foundation of China (National Science Foundation of China) U21A20376Natural Science Foundation of Hubei Province (Hubei Provincial Natural Science Foundation) 2025AFA104
6 · The paper itself

Abstract

Immune checkpoint inhibitor (ICI) resistance in hepatocellular carcinoma (HCC) poses a major therapeutic challenge. Here we present a Phase 2 trial evaluating stereotactic body radiotherapy (SBRT) combined with sintilimab and bevacizumab biosimilar (PD-1/VEGF blockade) to overcome resistance in ICI-refractory HCC. Twenty-one patients with progressive HCC after ICI therapy receive SBRT followed by sintilimab 200 mg and bevacizumab biosimilar 15 mg/kg every 3 weeks. The primary outcome, objective response rate in non-irradiated lesions is 33.3%, with a disease control rate of 66.7%. Median progression-free survival is 6.2 months, and estimated median overall survival is 24.4 months. SBRT achieves 100% local control, with 33.3% experiencing grade 3 or higher adverse events. Proteomic profiling reveals that responders exhibit lower baseline IFN-γ and elevated IL-6, while post-SBRT increases in IFN-γ, IL-2, and IL-6 correlate with improved outcomes. These results indicate that combination of SBRT in ICI-refractory HCC is effective, well-tolerated, and may be guided by cytokine assessment.

Indexed as

Antibodies, Monoclonal, HumanizedBevacizumabBiosimilar PharmaceuticalsCarcinoma, HepatocellularLiver NeoplasmsRadiosurgeryAdultAgedCombined Modality TherapyDrug Resistance, NeoplasmFemaleHumansImmune Checkpoint InhibitorsMaleMiddle AgedProgrammed Cell Death 1 ReceptorAntibodies, Monoclonal, HumanizedBevacizumabBiosimilar PharmaceuticalsImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorsintilimab

Identifiers

PMID41413036
PMCPMC12823611

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.