Evidence map›Paper›PMID 34824161›Full record

ArticleJournal for immunotherapy of cancer2021

Low peripheral blood derived neutrophil-to-lymphocyte ratio (dNLR) is associated with increased tumor T-cell infiltration and favorable outcomes to first-line pembrolizumab in non-small cell lung cancer.

Joao V Alessi, Biagio Ricciuti, Stephanie L Alden, Arrien A Bertram, Jessica J Lin, Mustafa Sakhi, Mizuki Nishino, Victor R Vaz, James Lindsay, Madison M Turner and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 2 pooled it
6.6field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 2 syntheses or guidelines pooled it, 94 citations in OpenAlex.

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21 more citing papers are in PubMed but not listed here.

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

16 authors at 4 institutions in 1 country.

Joao V AlessiLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.ORCID 0000-0002-8072-5946
Biagio RicciutiLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.ORCID 0000-0002-0651-2678
Stephanie L AldenDepartment of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Arrien A BertramLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Jessica J LinDepartment of Medicine, Massachusetts General Hospital Cancer Center, Boston, Massachusetts, USA.
Mustafa SakhiDepartment of Medicine, Massachusetts General Hospital Cancer Center, Boston, Massachusetts, USA.
Mizuki NishinoDepartment of Radiology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Victor R VazLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
James LindsayKnowledge Systems Group, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Madison M TurnerImmunoProfile, Brigham & Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Kathleen PfaffImmunoProfile, Brigham & Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Bijaya SharmaImmunoProfile, Brigham & Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Kristen D FeltImmunoProfile, Brigham & Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Scott J RodigDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Justin F GainorDepartment of Medicine, Massachusetts General Hospital Cancer Center, Boston, Massachusetts, USA.
Mark M AwadLowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA mark_awad@dfci.harvard.edu.ORCID 0000-0003-0928-5244
Brigham and Women's Hospital · USDana-Farber Cancer Institute · USMassachusetts General Hospital · USHarvard University · US

Funding

The Boston Lung Cancer Survival CohortU01CA209414 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI David C Christiani · 2017 to 2026
$12.2M
Automated in vivo analysis of tumor growth rate as a guide for therapeutic decisions to advance personalized cancer treatmentR01CA203636 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI NISHINO, MIZUKI · 2017 to 2021
$2.9M
NCI NIH HHS R01 CA203636NCI NIH HHS U01 CA209414
6 · The paper itself

Abstract

backgroundAn elevated peripheral blood derived neutrophil-to-lymphocyte ratio (dNLR) is a negative prognostic marker for patients with non-small cell lung cancer (NSCLC) receiving chemotherapy and immune checkpoint inhibitors. Whether dNLR is also associated with clinical outcomes to first-line pembrolizumab among patients with NSCLC and a programmed cell death ligand 1 (PD-L1) Tumor Proportion Score (TPS) of ≥50% is uncertain. How dNLR relates to the tumor immune microenvironment is also unclear.

methodsIn two participating academic centers, we retrospectively analyzed the dNLR (defined as the absolute neutrophil count/white cell count - absolute neutrophil count) prior to initiation of first-line pembrolizumab in patients with metastatic NSCLC and a PD-L1 TPS ≥50% and lacking genomic alterations in

resultsA total of 221 patients treated with first-line pembrolizumab were included in this study. The optimal dNLR cut-off to differentiate treatment responders from non-responders was 2.6. Compared with patients with a dNLR ≥2.6 (n=97), patients with dNLR <2.6 (n=124) had a significantly higher ORR (52.4% vs 24.7%, p<0.001), a significantly longer median progression-free survival (mPFS 10.4 vs 3.4 months, HR 0.48, 95% CI 0.35 to 0.66, p<0.001), and a significantly longer median overall survival (mOS 36.6 vs 9.8 months, HR 0.34, 95% CI 0.23 to 0.49, p<0.001). After adjusting for age, sex, tobacco use, performance status, histology, serum albumin level, oncogenic driver status, and PD-L1 distribution (50%-89% vs ≥90%), a dNLR <2.6 was confirmed to be an independent predictor of longer mPFS (HR 0.47, 95% CI 0.33 to 0.67, p<0.001) and mOS (HR 0.32, 95% CI 0.21 to 0.49, p<0.001). Among advanced NSCLC samples with a PD-L1 TPS of ≥50%, those with a dNLR <2.6 had significantly higher numbers of tumor-associated CD8+, FOXP3+, PD-1 +immune cells, and PD-1 +CD8+T cells than those with a dNLR ≥2.6.

conclusionsAmong patients with NSCLC and a PD-L1 TPS ≥50%, a low dNLR has a distinct immune tumor microenvironment and more favorable outcomes to first-line pembrolizumab.

Indexed as

AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedCarcinoma, Non-Small-Cell LungFemaleHumansLung NeoplasmsLymphocytesMaleMiddle AgedNeutrophilsRetrospective StudiesT-LymphocytesAntibodies, Monoclonal, Humanizedpembrolizumaband non-small cell lung cancerderived neutrophil-to-lymphocyte ratiomultiplexed immunofluorescencePD-L1 TPS ≥50%pembrolizumab

Identifiers

PMID34824161
PMCPMC8627393
OpenAlexW3217012599

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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.