Evidence map›Paper›PMID 40778089›Full record

ArticleClinical and translational radiation oncology2025

Simultaneous integrated boost and protection proton beam therapy approach for hepatocellular carcinoma.

Kanokphorn Thonglert, Matthew D Greer, Stephanie K Schaub, Stephen R Bowen, Anthony M Menghini, Matthew J Nyflot, Clemens Grassberger, Joseph Tsai, Peter Zaki, Edward Y Kim and 2 more

Abstract read
In one paragraph

Article in Clinical and translational radiation oncology, 2025. 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

12 authors.

Kanokphorn ThonglertDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Matthew D GreerDepartment of Radiation Oncology, University of Arizona Cancer Center, Tucson, AZ, United States.
Stephanie K SchaubDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Stephen R BowenDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Anthony M MenghiniDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Matthew J NyflotDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Clemens GrassbergerDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Joseph TsaiDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Peter ZakiDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Edward Y KimDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Tony WongDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.
Smith ApisarnthanaraxDepartment of Radiation Oncology, University of Washington School of Medicine, Seattle, WA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Although simultaneous integrated boost and protection with proton beam therapy (SIB-PBT) facilitates tumor dose escalation while maintaining organ-at-risk (OAR) dose constraints, clinical outcomes are limited. This study assessed the safety and efficacy of using the SIB-PBT technique in hepatocellular carcinoma (HCC) patients. Methods: We reviewed 47 patients with HCC who underwent SIB-PBT between 2014-2021. The radiation dose ranged from 36-67.5 Gy(RBE) in 15 fractions. SIB-PBT was used for the following reasons: minimize high-dose exposure to organs-at-risk (OARs) (n = 22, 47 %), treat targets with different dose levels (n = 6, 13 %), or both (n = 19, 40 %). Survival, local control, and toxicities were assessed using Kaplan-Meier, Fine-Gray cumulative incidence, and descriptive statistics, respectively. Results: Forty-one patients (87 %) had tumors located ≤2 cm from luminal gastrointestinal (GI) OARs. The median tumor diameter was 9.2 cm (range, 2.0-21.5 cm). The median EQD2 D50%, D95% and D99% of gross tumor volume were 79.8 (range, 51.1-85.9), 66.7 (range, 36.9-84.6) and 50.2 (range, 34.1-83.6) Gy(RBE) Conclusion: SIB-PBT enables OAR protection along with heterogeneous tumor dose escalation and is a safe and effective treatment for HCC tumors.

Indexed as

Hepatocellular carcinoma (HCC)Intensity modulated proton therapy (IMPT)Proton beam therapy (PBT)RadiotherapySimultaneous integrated boost/protection (SIB/SIP)

Identifiers

PMID40778089
PMCPMC12328680

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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.