Evidence map›Paper›PMID 38077640›Full record

ArticleWorld journal of gastrointestinal oncology2023

Baseline neutrophil-lymphocyte ratio and platelet-lymphocyte ratio appear predictive of immune treatment related toxicity in hepatocellular carcinoma.

Sirish Dharmapuri, Umut Özbek, Hiren Jethra, Tomi Jun, Thomas U Marron, Anwaar Saeed, Yi-Hsiang Huang, Mahvish Muzaffar, Matthias Pinter, Lorenz Balcar and 27 more

Open access · diamondAbstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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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

37 authors at 5 institutions in 4 countries.

Sirish DharmapuriTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States. sirish.dharmapuri@gmail.com.
Umut ÖzbekDepartment of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.
Hiren JethraDepartment of Data Analytics Harrisburg, Harrisburg University of Science and Technology, Harrisburd, PA 17101, United States.
Tomi JunSEMA4, Stamford, CT 06902, United States.
Thomas U MarronTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.
Anwaar SaeedDivision of Medical Oncology Kansas, University of Kansas Cancer Center, Kansas, MO 66160, United States.
Yi-Hsiang HuangDivision of Gastroenterology and Hepatology, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Mahvish MuzaffarDepartment of Internal Medicine, Brody School of Medicine, East Carolina University, Greenville, NC 27858, United States.
Matthias PinterDepartment of Internal Medicine III, Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna 1090, Austria.
Lorenz BalcarDepartment of Internal Medicine III, Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna 1090, Austria.
Claudia FulgenziDepartment of Surgery and Cancer, Imperial College London, Hammersmith Hospital London, London W12 0HS, United Kingdom.
Suneetha AmaraDepartment of Internal Medicine, Brody School of Medicine, East Carolina University, Greenville, NC 27858, United States.
Arndt WeinmannDepartment of Hepatology, Johannes Gutenberg-University Medical Centre, Niedersachsen 30625, Germany.
Nicola PersoneniMedical Oncology Unit, ASST Garda, Via Lungomella Valsecchi, Brescia, Manerbio 25025, Italy.
Bernhard ScheinerDepartment of Internal Medicine III, Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna 1090, Austria.
Tiziana PressianiMedical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Milan, Rozzano 20089, Italy.
Musharraf NavaidDepartment of Internal Medicine, Brody School of Medicine, East Carolina University, Greenville, NC 27858, United States.
Bertram BengschDepartment of Medicine II, Univ Med Ctr Freiburg, Hugstetter Str 55, University Hospital Freiburg, Freiburg D-79106, Germany.
Sonal PaulDepartment of Oncology Baltimore, LifeBridge Health, Baltimore, MD 21215, United States.
Uqba KhanDivision of Hematology and Oncology, Weill Cornell Medical College, NY 10065, United States.
Dominik BettingerDepartment of Medicine II, Univ Med Ctr Freiburg, Hugstetter Str 55, University Hospital Freiburg, Freiburg D-79106, Germany.
Naoshi NishidaDepartment of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka 577-8502, Japan.
Yehia Ibrahim MohamedDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
Arndt VogelDepartment of Gastroenterology Hepatology and Endocrinology, HannoverArndt Vogel, Medical School Hannover, Carl-Neubergstr., Hannover 30659, Germany.
Anuhya GampaDepartment of Hepatology, Rush University Medical Group 1725 W Harrison St Ste 158, Chicago, IL 60612, United States.
James KorolewiczDepartment of Surgery and Cancer, Imperial College London, Hammersmith Hospital London, London W12 0HS, United Kingdom.
Antonella CammarotaMedical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Milan, Rozzano 20089, Italy.
Ahmed KasebDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
Peter R GalleDepartment of Internal Medicine I and Cirrhosis Center Mainz, University Medical Center Mainz, Johannes Gutenberg Univ Mainz, Med Klin and Poliklin, Mainz D-55131, Germany.
Anjana PillaiDepartment of Gastroenterology, Hepatology, and Nutrition, University of Chicago Medical Center, Chicago, IL 60637, United States.
Ying-Hong WangDepartment of Gastroenterology, Hepatology and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
Alessio CortelliniDepartment of Surgery and Cancer, Imperial College London, Hammersmith Hospital London, London W12 0HS, United Kingdom.
Masatoshi KudoDepartment of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka 577-8502, Japan.
Antonio D'AlessioDepartment of Surgery and Cancer, Imperial College London, Hammersmith Hospital London, London W12 0HS, United Kingdom.
Lorenza RimassaMedical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Milan, Rozzano 20089, Italy.
David James PinatoDepartment of Surgery and Cancer, Imperial College London, Hammersmith Hospital London, London W12 0HS, United Kingdom.
Celina AngTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.
Hammersmith Hospital · GBIcahn School of Medicine at Mount Sinai · USMedical University of Vienna · ATKindai University · JPThe University of Texas MD Anderson Cancer Center · US

Funding

THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Ramon E Parsons · 2015 to 2026
$35.4M
NCI NIH HHS P30 CA196521
6 · The paper itself

Abstract

backgroundA well-recognized class effect of immune checkpoint inhibitors (ICI) is immune-related adverse events (IrAEs) ranging from low grade toxicities to life-threatening end organ damage requiring permanent discontinuation of ICI. Deaths are reported in < 5% of patients treated with ICI. There are, however, no reliable markers to predict the onset and severity of IrAEs. We tested the association between neutrophil-lymphocyte ratio (NLR) and platelet-lymphocyte ratio (PLR) at baseline with development of clinically significant IrAEs (grade ≥ 2) in hepatocellular carcinoma (HCC) patients treated with ICI.

aimTo test the association between NLR and PLR at baseline with development of clinically significant IrAEs (grade ≥ 2) in HCC patients treated with ICI.

methodsData was extracted from an international database from a consortium of 11 tertiary-care referral centers. NLR = absolute neutrophil count/absolute lymphocyte count (ALC) and PLR = platelet count/ALC. Cutoff of 5 was used for NLR and 300 for PLR based on literature. We also tested the association between antibiotic and steroid exposure to IrAEs.

resultsData was collected from 361 patients treated between 2016-2020 across the United States (67%), Asia (14%) and Europe (19%). Most patients received Nivolumab (

conclusionGiven that high baseline NLR and PLR are associated with a decreased incidence of IrAEs, lower baseline NLR and PLR may be predictive biomarkers for the appearance of IrAEs in HCC treated with ICI. This finding is in keeping with several studies in solid tumors that have shown that baseline NLR and PLR appear predictive of IrAEs.

Indexed as

Immune toxicityImmunotherapyInflammatory biomarkersNeutrophil-lymphocyte ratioPlatelet-lymphocyte ratio

Identifiers

PMID38077640
PMCPMC10701235
OpenAlexW4388680826

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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.