Evidence map›Paper›PMID 39516856›Full record

ArticleRadiation oncology (London, England)2024

Prognostic value of neutrophil to lymphocyte ratio and lymphocyte counts before durvalumab consolidation after radio-chemotherapy in locally advanced non-small cell lung cancer.

Arnaud Colomb, Benoit Allignet, Mehdi Lamkhioued, Aurelie Swalduz, Lionel Falchero, Aurélie Kienlen, Michaël Duruisseaux, Coralie Moncharmont

Abstract read
In one paragraph

Article in Radiation oncology (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

8 authors.

Arnaud ColombDepartment of Radiation Oncology, Centre Léon Bérard, 28 rue Laennec, Lyon, 69673, France. arnaud.colomb425@gmail.com.
Benoit AllignetDepartment of Radiation Oncology, Centre Léon Bérard, 28 rue Laennec, Lyon, 69673, France.
Mehdi LamkhiouedPneumology Departement, Centre Hospitalo-Universitaire de Lyon sud, Hospices Civils de Lyon, Lyon, France.
Aurelie SwalduzPneumology Departement, Centre Léon Bérard, 28 rue Laennec, Lyon, 69673, France.
Lionel FalcheroPneumology Departement, Centre Hospitalier de Villefranche de Rouergue, Villefranche, France.
Aurélie KienlenPneumology Departement, CHU de Saint-Pierre, Saint-Pierre, France.
Michaël DuruisseauxRespiratory Department and Early Phase, Louis Pradel Hospital, Hospices Civils de Lyon Cancer Institute, Lyon, France.
Coralie MoncharmontDepartment of Radiation Oncology, Centre Léon Bérard, 28 rue Laennec, Lyon, 69673, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDurvalumab, an anti-PD-L1 immune checkpoint inhibitor, after radio-chemotherapy (RCT) has changed the management of locally advanced non-small cell lung cancer (LA NSCLC). A series of retrospective studies have investigated different cut-off of lymphocyte count (LyC) and neutrophil-to-lymphocyte ratio (NLR) to predict survival in LA NSCLC. None of these studies has validated their threshold in an independent group of patients. We wanted to assess the OS prognostic value of NLR and LyC in patients with LA NSCLC treated by RCT and durvalumab, with threshold determination and their validation in an external cohort.

methodsPatients were enrolled in four institutions between Oct. 2017 and Jan. 2022. Pre durvalumab LyC, neutrophils count (NC) and NLR were collected. To define NLR and LyC cut-off value predicting survival event, time dependent Receiver Operating Characteristics (ROC) curves was performed. Survival outcomes were estimated by the Kaplan-Meier method and differences were compared using univariate and multivariate Cox proportional hazard models.

resultsWe included 76 patients in the training set and 85 in the test set. The best cut off were 2,94 for NLR and 0,61 G/l for LyC to predict OS in the training set. For patients with NLR > 2,94, univariate analysis showed no significant deterioration in OS in either the training set (p = 0,066) or the test set (p = 0,12). Patients with LyC > 0,61 G/L, in univariate analysis, had longer OS in training set (p = 0,030) and in test set (p = 0,0062). This OS increase was not found in multivariate analysis (p = 0,057) in training set but was confirmed in test set (0,039).

conclusionLyC > 0,61 G/l is associated with longer OS for LA NSCLC patient's treated with RCT and durvalumab in univariate analysis. In this context, a particular expectation for organs at risk sparing during RT to avoid lymphopenia seems important.

trial registrationRetrospectively registered.

Indexed as

Antibodies, MonoclonalCarcinoma, Non-Small-Cell LungChemoradiotherapyLung NeoplasmsLymphocytesNeutrophilsAdultAgedAged, 80 and overAntineoplastic Agents, ImmunologicalFemaleHumansLymphocyte CountMaleMiddle AgedPrognosisAntibodies, MonoclonalAntineoplastic Agents, ImmunologicaldurvalumabDurvalumab consolidationLocally advanced non-small cell lung cancerLymphocytes countNeutrophil to lymphocytesOverall survivalRadio-chemotherapy

Identifiers

PMID39516856
PMCPMC11545521

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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.