Evidence map›Paper›PMID 40126606›Full record

ArticleEuropean radiology2025

Synthetic tumor extracellular volume as a predictive biomarker for colorectal liver metastasis patients prior to curative hepatectomy.

Kiyoyuki Minamiguchi, Harufumi Maki, Antony Haddad, Andrea C Cortes, Mateo Lendoire, Toshihiro Tanaka, Marshall E Hicks, Jean-Nicolas Vauthey, Rony Avritscher

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Article in European radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Kiyoyuki MinamiguchiDepartment of Interventional Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Harufumi MakiDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Antony HaddadDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Andrea C CortesDepartment of Interventional Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Mateo LendoireDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Toshihiro TanakaDepartment of Diagnostic and Interventional Radiology, Nara Medical University, Kashihara, Nara, Japan.
Marshall E HicksDepartment of Interventional Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jean-Nicolas VautheyDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Rony AvritscherDepartment of Interventional Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. rony.avritscher@mdanderson.org.ORCID http://orcid.org/0000-0002-5122-3445

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30CA016672
6 · The paper itself

Abstract

objectiveThis study evaluated the prognostic value of synthetic tumor extracellular volume fraction (ECV) and its association with somatic gene alternations in patients with colorectal liver metastases (CRLM) receiving neoadjuvant chemotherapy.

methodsThis retrospective single-center study included patients undergoing curative hepatectomy after neoadjuvant chemotherapy for CRLM (2013-2020). Contrast-enhanced computed tomography (CT) studies obtained after neoadjuvant chemotherapy were used to calculate synthetic ECV and synthetic hematocrit by linear regression analysis. Patients were grouped according to synthetic ECV cutoff point based on the Youden index. Multivariate analyses were performed with Cox regression models to analyze the prognostic factors of overall survival (OS) and recurrence-free survival (RFS).

resultsA total of 209 patients (median age 56 years, 119 men) were enrolled. Synthetic ECV correlated well with conventional ECV (r = 0.996, p < 0.0001) with minimal bias, according to the Bland-Altman analysis (bias = 0.007). The optimal synthetic ECV cutoff point was determined to be 21%, with 115 patients having high ECV and 94 low ECV. Multivariable analysis for predicting high ECV demonstrated significant associations with synchronous CRLM, anti-VEGF agent-containing regimen, and RAS-BRAF mutation (p = 0.022, < 0.001, and = 0.003, respectively). OS and RFS were significantly higher in the high ECV group compared to the low ECV group (p = 0.019 and p = 0.015, respectively). High ECV was independently associated with improved OS (HR 0.55, 95% CI 0.34-0.91) and RFS (HR 0.71, 95% CI 0.52-0.97).

conclusionsSynthetic ECV can help predict OS and RFS in patients undergoing curative-intent CRLM resection after neoadjuvant chemotherapy and could be a useful imaging biomarker to stratify risk. KEY POINTS: Question There is a need for a biomarker predictive of treatment response after neoadjuvant chemotherapy, prior to curative-intent colorectal liver metastases. Findings Synthetic extracellular volume fraction can help predict overall and recurrence-free survival and is associated with somatic gene alterations. Clinical relevance Prognostic markers of response to neoadjuvant chemotherapy in curative-intent colorectal liver metastases include extracellular volume fraction. Synthetic extracellular volume fraction obviates the need for hematocrit; a simplification that is expected to streamline routine clinical practice.

Indexed as

Colorectal NeoplasmsHepatectomyLiver NeoplasmsTomography, X-Ray ComputedAdultAgedBiomarkers, TumorContrast MediaFemaleHumansMaleMiddle AgedNeoadjuvant TherapyPredictive Value of TestsPrognosisRetrospective StudiesBiomarkers, TumorContrast MediaBody fluid compartmentsColorectal neoplasmsExtracellular volumePrognostic factor

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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.