Evidence map›Paper›PMID 39090596›Full record

ArticleBMC cancer2024

The influence of nutritional status, lipid profile, leptin concentration and polymorphism of genes encoding leptin and neuropeptide Y on the effectiveness of immunotherapy in advanced NSCLC patients.

Małgorzata Frąk, Anna Grenda, Paweł Krawczyk, Barbara Kuźnar-Kamińska, Paweł Pazdrowski, Karolina Kędra, Izabela Chmielewska, Janusz Milanowski

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
–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

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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Regulatory polymorphisms ofJournal for immunotherapy of cancer · 2025
    Article
  7. Review
  8. Review
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

8 authors.

Małgorzata FrąkDepartment of Pneumonology, Oncology and Allergology Medical, University of Lublin, Jaczewskiego 8, Lublin, 20-954, Poland. malgorzata.frak@gmail.com.
Anna GrendaDepartment of Pneumonology, Oncology and Allergology Medical, University of Lublin, Jaczewskiego 8, Lublin, 20-954, Poland. anna.grenda@umlub.pl.
Paweł KrawczykDepartment of Pneumonology, Oncology and Allergology Medical, University of Lublin, Jaczewskiego 8, Lublin, 20-954, Poland.
Barbara Kuźnar-KamińskaDepartment of Pulmonology, Allergology and Pulmonary Oncology, Poznan University of Medical Sciences, Poznań, Poland.
Paweł PazdrowskiDepartment of Head, Neck Surgery and Laryngological Oncology, Poznan University of Medical Sciences, Poznań, Poland.
Karolina KędraInstitute of Physical Chemistry, Polish Academy of Sciences in Warsaw, Warsaw, Poland.
Izabela ChmielewskaDepartment of Pneumonology, Oncology and Allergology Medical, University of Lublin, Jaczewskiego 8, Lublin, 20-954, Poland.
Janusz MilanowskiDepartment of Pneumonology, Oncology and Allergology Medical, University of Lublin, Jaczewskiego 8, Lublin, 20-954, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNeuropeptide Y is a neurotransmitter in the nervous system and belongs to the orexigenic system that increases appetite. Its excessive secretion leads to obesity. Leptin is a pro-inflammatory adipokine (produced in adipose tissue) induced in obesity and may mediate increased antitumor immunity in obesity (including the promotion of M1 macrophages). Leptin and neuropeptide Y gene polymorphisms, causing increased leptin levels and the occurrence of obesity, and lipid profile disorders, may increase the effectiveness of immunotherapy. MATERIALS AND

methodsIn 121 patients with advanced NSCLC without mutations in the EGFR gene and rearrangements of the ALK and ROS1 genes, undergoing immunotherapy (1st and 2nd line of treatment) or chemoimmunotherapy (1st line of treatment), we assessed BMI, lipid profile, PD-L1 expression on cancer cells using the immunohistochemical method (clone SP263 antibody), leptin concentration in blood serum by ELISA, polymorphisms in the promoter region of the genes for leptin (LEP) and neuropeptide Y (NPY) by real-time PCR.

resultsLeptin concentration was significantly higher in obese patients than in patients with normal or low weight (p = 0.00003) and in patients with disease stabilization compared to patients with progression observed during immunotherapy (p = 0.012). Disease control occurred significantly more often in patients with the GA or AA genotype than patients with the GG genotype in the rs779039 polymorphism of the LEP gene. The median PFS in the entire study group was five months (95% CI: 3-5.5), and the median OS was 12 months (95% CI: 8-16). Median PFS was highest in patients with TPS ≥ 50% (6.5 months) and in obese patients (6.6 months). Obese patients also had a slightly longer median OS compared to other patients (23.8 vs. 13 months). The multivariate Cox logistic regression test showed that the only factor reducing the risk of progression was TPS ≥ 50% (HR = 0.6068, 95% CI: 0.4001-0.9204, p = 0, 0187), and the only factor reducing the risk of death was high leptin concentration (HR = 0.6743, 95% CI: 0.4243-1.0715, p = 0.0953).

conclusionAssessment of nutritional status, serum leptin concentration and polymorphisms in the LEP gene may be of additional importance in predicting the effectiveness of immunotherapy and chemoimmunotherapy in patients with advanced NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungImmunotherapyLeptinLung NeoplasmsNeuropeptide YNutritional StatusAdultAgedAged, 80 and overB7-H1 AntigenFemaleHumansLipidsMaleMiddle AgedObesityB7-H1 AntigenCD274 protein, humanLEP protein, humanLeptinLipidsNeuropeptide YImmunotherapyLeptinLipid profileNon-small cell lung cancerObesity

Identifiers

PMID39090596
PMCPMC11295594

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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.