Evidence map›Paper›PMID 32128703›Full record

ArticleJournal of gastrointestinal cancer2021

Evaluation of Ferritin and Transferrin Ratio as a Prognostic Marker for Hepatocellular Carcinoma.

Ishaan Vohra, Bashar Attar, Vatsala Katiyar, Pedro Palacios, Tejinder Randhawa, Muhammad Arslan Baig, Estefania Flores, Yuchen Wang, Hemant Mutneja, Sachit Sharma and 6 more

Abstract read
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In one paragraph

Article in Journal of gastrointestinal cancer, 2021. 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
0.3field-weighted citation impact, top 51% of its field
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, 7 citations in OpenAlex.

  1. Review
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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 at 3 institutions in 1 country.

Ishaan VohraDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA. ishaan.vohra@cookcountyhhs.org.ORCID https://orcid.org/0000-0002-9715-8829
Bashar AttarDivision of Gastroenterology and Hepatology, Department of Medicine, Cook County Health and Hospital System, County, Chicago, IL, USA.
Vatsala KatiyarDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA.
Pedro PalaciosDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA.
Tejinder RandhawaDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA.
Muhammad Arslan BaigDivision of Gastroenterology and Hepatology, Department of Medicine, University of Illinois at Chicago, Peoria, IL, USA.
Estefania FloresDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA.
Yuchen WangDivision of Gastroenterology and Hepatology, Department of Medicine, Cook County Health and Hospital System, County, Chicago, IL, USA.
Hemant MutnejaDivision of Gastroenterology and Hepatology, Department of Medicine, Cook County Health and Hospital System, County, Chicago, IL, USA.
Sachit SharmaDepartment of Medicine, University of Toledo, Toledo, OH, USA.
Prashanth LingamneniDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA.
Muhammad Zain FarooqDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA.
Naveen BhaskaranDepartment of Medicine, Cook County Health and Hospital System, 1900 West Polk Street, 15th Floor, Chicago, IL, 60612, USA.
Seema GandhiDivision of Gastroenterology and Hepatology, Department of Medicine, Cook County Health and Hospital System, County, Chicago, IL, USA.
Gijo VettiankalDivision of Gastroenterology and Hepatology, Department of Medicine, Cook County Health and Hospital System, County, Chicago, IL, USA.
Melchor DemetriaDivision of Gastroenterology and Hepatology, Department of Medicine, Cook County Health and Hospital System, County, Chicago, IL, USA.
Cook County Health and Hospitals System · USUniversity of Illinois Chicago · USUniversity of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of the studyHepatocellular carcinoma (HCC) has tripled in incidence over the past 20 years and now ranks as the third leading cause of mortality attributed to cancer. Underlying pathophysiology is sustained hepatic inflammation which results in hepatocellular dysplasia and thus an environment prone to HCC. Considering the essential role of inflammation in the pathogenesis of HCC, we evaluated the prognostic utility of ferritin-transferrin ratio (FTR) in HCC.

methodsWe retrospectively reviewed the electronic medical records of patients with HCC (diagnosed on radiographic criteria and/or biopsy) from 2000 through 2015. We collected data regarding the patient demographics, laboratory investigations at the time of HCC diagnosis and prior to the initiation of treatment. Overall survival was calculated from the time of diagnosis, cases were censored at the date of last follow-up, if date of death was not known. Kaplan-Meier curves were estimated to evaluate the prognostic significance of FTR. Receiver operating characteristics (ROC) curve was plotted for FTR to predict mortality and identify cut-off value by optimized Youden's index.

resultsAmong the 176 patients identified by initial screening, 116 patients were eventually included for analysis. Overall median survival was 11.9 months. FTR, of note, was significantly lower in alive (6.9, p < 0.001). In univariate analysis, alfa-fetoprotein (AFP), aspartate aminotransferase (AST), serum ferritin (SF), transferrin (TFS), and FTR were significantly associated with mortality. On multivariate analysis for mortality, FTR, AFP, and epidemiologic factors predictive of mortality including male gender and advanced HCC were significant.

conclusionThe ferritin-transferrin ratio (FTR), calculated at the time of HCC diagnosis could predict mortality in our cohort of patients. With an optimal cut-off of 7.7 for FTR were stratified into high- and low-risk groups. The hazard ratio between the two groups was 2.36 (p < 0.003). Future studies with longitudinal follow-up of FTR at intervals and important time points (e.g., perioperative) might provide more insights to its prognostic value.

Indexed as

AgedBiomarkers, TumorCarcinoma, HepatocellularFeasibility StudiesFemaleFerritinsFollow-Up StudiesHumansKaplan-Meier EstimateLiver NeoplasmsMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesRisk FactorsBiomarkers, TumorFerritinsTransferrinAFPFerritin transferrin ratioFTRHCCSerum ferritinSFTransferrin TFS

Identifiers

PMID32128703
OpenAlexW3009689644

What OpenQuestion holds

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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 OpenQuestion graph.