Evidence map›Paper›PMID 39164973›Full record

ArticleCancer medicine2024

The prevalence and prognostic value of systemic inflammation in good performance status patients with advanced, inoperable non-small cell lung cancer receiving palliative radiotherapy: Comparison of composite ratios and cumulative scores.

Josh McGovern, Fraser O'Rourke, Sarah Will, Hanh Thi Ngoc Nguyen, Elise Cranfield, Charlotte Maseland, Nicholas MacLeod, John D Maclay, Barry J Laird, Ross D Dolan and 1 more

Abstract read
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Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

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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

5 citing papers in PubMed.

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4 · The record

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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

11 authors.

Josh McGovernAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.ORCID 0000-0002-6889-6240
Fraser O'RourkeAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.
Sarah WillAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.
Hanh Thi Ngoc NguyenAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.
Elise CranfieldAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.
Charlotte MaselandAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.
Nicholas MacLeodDepartment of Oncology, Beatson West of Scotland Cancer Centre, Glasgow, UK.
John D MaclayDepartment of Respiratory Medicine, Glasgow Royal Infirmary, Glasgow, UK.
Barry J LairdInstitute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Ross D DolanAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.
Donald C McMillanAcademic Unit of Surgery, University of Glasgow, Glasgow, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe present study sought to examine the relationships between systemic inflammatory composite ratios/cumulative scores, magnitude of systemic inflammatory response (SIR) and survival in good performance status patients (ECOG-PS 0/1) with advanced NSCLC receiving palliative radiotherapy.

methodsSystemic inflammatory composite ratios/cumulative scores included the neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), lymphocyte-monocyte ratio (LMR), C-reactive protein, (CRP)-albumin ratio (CAR), neutrophil- lymphocyte score (NLS), platelet-lymphocyte score (PLS), lymphocyte-monocyte score (LMS), neutrophil-platelet score (NPS), modified Glasgow prognostic score (mGPS). The magnitude of SIR was determined by serum CRP concentration, with a median CRP concentration of >10 m mg/L considered to be systemically inflamed. Relationships between systemic inflammatory composite ratios/ cumulative scores and clinicopathological characteristics were examined using chi-square analysis. Relationships between overall survival (OS) and systemic inflammatory composite ratios/ cumulative scores were examined using cox regression analysis.

results479 patients were included. 48% (n = 231) of patients were male and 70% (n = 338) were ≥65 years of age. 29% (n = 140) patients were ECOG-PS 0 and 71% (n = 339) were ECOG-PS 1. 98% (n = 469) of patients died during follow-up. The median survival was 5 months (2-11). A similar prevalence of systemic inflammation was noted across the various ratios/scores (NLR >3 68%; LMR <2.4 65%; PLR >150 70%; CAR >0.20 83%; NLS ≥1 66%; LMS ≥1 71%; NPS≥1 50%; PLS≥1 60% and mGPS≥1 75%). Despite not considered to be systemically inflamed, an NLR <3, LMR ≥2.4, PLR ≤150, NLS 0, LMS 0, NPS 0 and PLS 0 all had a median CRP concentration of >10 mg/L. When adjusted for ECOG-PS, CAR>0.40 (p < 0.001) and mGPS 2 (p < 0.05) remained significantly associated with OS.

conclusionLiver-based measures of systemic inflammation (CAR and mGPS) appear more reliable for the quantification of the magnitude of SIR and have prognostic value in patients with advanced NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungInflammationLung NeoplasmsPalliative CareAdultAgedAged, 80 and overBlood PlateletsC-Reactive ProteinFemaleHumansLymphocytesMaleMiddle AgedMonocytesNeoplasm StagingC-Reactive ProteincancerinflammationNSCLCsurvival

Identifiers

PMID39164973
PMCPMC11335809

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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.