Evidence map›Paper›PMID 37385234›Full record

ArticleDigestive diseases (Basel, Switzerland)2023

Interstitial Brachytherapy for Hepatocellular Carcinoma: Analysis of Prognostic Factors for Overall Survival and Progression-Free Survival and Application of a Risk Stratification Model.

Maximilian Thormann, Franziska Heitmann, Vanessa Wrobel, Constanze Heinze, Christine March, Peter Hass, Robert Damm, Alexey Surov, Maciej Pech, Jazan Omari

Abstract read
In one paragraph

Article in Digestive diseases (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Maximilian ThormannDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Franziska HeitmannDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Vanessa WrobelDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Constanze HeinzeDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Christine MarchDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Peter HassDepartment of Radiation Oncology, University Hospital Magdeburg, Magdeburg, Germany.
Robert DammDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Alexey SurovDepartment of Radiology, Neuroradiology and Nuclear Medicine, Johannes Wesling University Hospital, Ruhr University Bochum, Minden, Germany.
Maciej PechDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Jazan OmariDepartment of Radiology and Nuclear Medicine, University Hospital Magdeburg, Magdeburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInterstitial brachytherapy (iBT) is an effective treatment for hepatocellular carcinoma (HCC). Identification of prognostic factors is pivotal for patient selection and treatment efficacy. This study aimed to assess the impact of low skeletal muscle mass (LSMM) on overall survival (OS) and progression-free survival (PFS) of iBT in patients with HCC.

methodsFor this single-center study, we retrospectively identified 77 patients with HCC who underwent iBT between 2011 and 2018. Follow-up visits were recorded until 2020. The psoas muscle area, psoas muscle index, psoas muscle density (MD), and the skeletal muscle gauge were assessed on the L3 level on pre-treatment cross-sectional CT scans.

resultsMedian OS was 37 months. 42 patients (54.5%) had LSMM. An AFP level of >400 ng/ml (hazard ratio [HR] 5.705, 95% confidence interval [CI]: 2.228-14.606, p = 0.001), BCLC stage (HR 3.230, 95% CI: 0.972-10.735, p = 0.026), and LSMM (HR 3.365, 95% CI: 1.490-7.596, p = 0.002) showed a relevant association with OS. Weighted hazard ratios were used to form a predictive risk stratification model with three groups: patients with low risk (median OS 62 months), intermediate risk (median OS 31 months), and high risk (median OS 9 months). The model showed a good prediction of 1-year mortality, with an AUC of 0.71. Higher MD was associated with better PFS (HR 0.920, 95% CI: 0.881-0.962, p < 0.001).

conclusionIn patients undergoing iBT for HCC, LSMM is associated with worse OS. A risk stratification model based on LSMM, AFP >400 ng/mL, and BCLC stage successfully predicted patient mortality. The model may support and enhance patient selection.

Indexed as

BrachytherapyCarcinoma, HepatocellularLiver Neoplasmsalpha-FetoproteinsHumansPrognosisProgression-Free SurvivalRetrospective StudiesRisk Assessmentalpha-FetoproteinsHepatocellular carcinomaInterstitial brachytherapyLow skeletal muscle massOverall survivalPrognostic modelProgression-free survival

Identifiers

PMID37385234
PMCPMC10716867

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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.