Evidence map›Paper›PMID 36051098›Full record

ArticleWorld journal of gastrointestinal oncology2022

Neutrophile-to-lymphocyte, lymphocyte-to-monocyte, and platelet-to-lymphocyte ratios as prognostic and response biomarkers for resectable locally advanced gastric cancer.

Tiago Cruz Tomás, Inês Eiriz, Marina Vitorino, Rodrigo Vicente, João Gramaça, Alicia Guadalupe Oliveira, Paulo Luz, Mafalda Baleiras, Ana Sofia Spencer, Luísa Leal Costa and 8 more

Open access · diamondAbstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 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

18 authors at 12 institutions in 1 country.

Tiago Cruz TomásDepartment of Medical Oncology, Hospital Professor Doutor Fernando Fonseca EPE, Amadora 2720-276, Portugal. tiago.tomas@campus.ul.pt.
Inês EirizDepartment of Medical Oncology, Hospital Professor Doutor Fernando Fonseca EPE, Amadora 2720-276, Portugal.
Marina VitorinoDepartment of Medical Oncology, Hospital Professor Doutor Fernando Fonseca EPE, Amadora 2720-276, Portugal.
Rodrigo VicenteDepartment of Medical Oncology, Hospital Professor Doutor Fernando Fonseca EPE, Amadora 2720-276, Portugal.
João GramaçaDepartment of Medical Oncology, Centro Hospitalar Barreiro-Montijo EPE, Barreiro 2830-003, Portugal.
Alicia Guadalupe OliveiraDepartment of Medical Oncology, Hospital do Espírito Santo de Évora EPE, Évora 7000-811, Portugal.
Paulo LuzDepartment of Medical Oncology, Centro Hospitalar Universitário do Algarve EPE, Algarve 8000-386, Portugal.
Mafalda BaleirasDepartment of Medical Oncology, Hospital São Francisco Xavier, Centro Hospitalar Lisboa Ocidental EPE, Lisboa 1449-005, Portugal.
Ana Sofia SpencerDepartment of Medical Oncology, Hospital Santo António dos Capuchos, Centro Hospital Lisboa Central EPE, Lisboa 1169-050, Portugal.
Luísa Leal CostaDepartment of Medical Oncology, Hospital Beatriz Ângelo, Loures 2674-514, Portugal.
Patrícia LiuDepartment of Medical Oncology, Centro Hospitalar de Trás-os-Montes e Alto Douro EPE, Vila Real 5000-508, Portugal.
Joana MendonçaDepartment of Medical Oncology, Hospital da Senhora da Oliveira EPE, Guimarães 4835-044, Portugal.
Magno DinisDepartment of Medical Oncology, Hospital Garcia de Orta EPE, Almada 2805-267, Portugal.
Teresa PadrãoDepartment of Medical Oncology, Hospital da Luz, Lisboa 1500-650, Portugal.
Marisol CorreiaDepartment of Medical Oncology, Hospital Distrital de Santarém EPE, Santarém 2005-177, Portugal.
Gonçalo AtalaiaDepartment of Medical Oncology, Hospital Professor Doutor Fernando Fonseca EPE, Amadora 2720-276, Portugal.
Michelle SilvaDepartment of Medical Oncology, Hospital Professor Doutor Fernando Fonseca EPE, Amadora 2720-276, Portugal.
Teresa FiúzaDepartment of Medical Oncology, Hospital Professor Doutor Fernando Fonseca EPE, Amadora 2720-276, Portugal.
Hospital Prof. Dr. Fernando Fonseca · PTAlgarve Biomedical Center · PTCentro De Medicina Veterinária Anjos De Assis · PTCentro Hospitalar de Lisboa Ocidental · PTHospital Beatriz Ângelo · PTHospital da Luz · PTHospital da Senhora da Oliveira Guimarães · PTHospital do Espírito Santo · PTHospital Garcia de Orta · PTHospital Santo António dos Capuchos · PTInstituto Politécnico de Santarém · PTUnidade Local de Saúde de Trás-os-Montes e Alto Douro · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPerioperative fluorouracil plus leucovorin, oxaliplatin, and docetaxel (FLOT) improves prognosis in locally advanced gastric cancer (LAGC). Neutrophil-to-lymphocyte (NLR), lymphocyte-to-monocyte (LMR), and platelet-to-lymphocyte (PLR) ratios are prognostic biomarkers but not predictive factors.

aimTo assess blood ratios' (NLR, LMR and PLR) potential predictive response to FLOT and survival outcomes in resectable LAGC patients.

methodsThis was a multicentric retrospective study investigating the clinical potential of NLR, LMR, and PLR in resectable LAGC patients, treated with at least one preoperative FLOT cycle, from 12 Portuguese hospitals. Means were compared through non-parametric Mann-Whitney tests. Receiver operating characteristic curve analysis defined the cut-off values as: High PLR > 141 for progression and > 144 for mortality; high LMR > 3.56 for T stage regression (TSR). Poisson and Cox regression models the calculated relative risks/hazard ratios, using NLR, pathologic complete response, TSR, and tumor regression grade (TRG) as independent variables, and overall survival (OS) as the dependent variable.

resultsThis study included 295 patients (mean age, 63.7 years; 59.7% males). NLR was correlated with survival time (

conclusionHigher NLR is correlated with longer survival time. High LMR patients have a higher risk of decreasing T stage, whereas high PLR patients have higher odds of progressing under FLOT and dying. Patients with TSR and a pathological response have better OS and lower risk of dying.

Indexed as

Gastric cancerLymphocyte-to-monocyteNeutrophil-to-lymphocytePerioperative fluorouracil plus leucovorin, oxaliplatin, and docetaxelPlatelet-to-lymphocyteTumor regression grade

Identifiers

PMID36051098
PMCPMC9305575
OpenAlexW4284889046

What OpenQuestion holds

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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.