Evidence map›Paper›PMID 28056941›Full record

ArticleBMC urology2017

Neutrophil-lymphocyte ratio as a predictive biomarker for response to high dose interleukin-2 in patients with renal cell carcinoma.

James A Kuzman, David D Stenehjem, Joseph Merriman, Archana M Agarwal, Shiven B Patel, Andrew W Hahn, Anitha Alex, Dan Albertson, David M Gill, Neeraj Agarwal

Abstract read
In one paragraph

Article in BMC urology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

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

  1. Pooled it
  2. Pooled it
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  15. Article
  16. IL-2 and Beyond in Cancer Immunotherapy.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2018
    Review
  17. Prospects of IL-2 in Cancer Immunotherapy.BioMed research international · 2018
    Review
  18. Article
  19. Evolving Treatment Paradigm in Metastatic Renal Cell Carcinoma.American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting · 2017
    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

10 authors.

James A KuzmanUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
David D StenehjemUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Joseph MerrimanUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Archana M AgarwalDepartment of Pathology and ARUP Laboratories, University of Utah, Salt Lake City, UT, USA.
Shiven B PatelUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Andrew W HahnUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Anitha AlexUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Dan AlbertsonUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
David M GillUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Neeraj AgarwalUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA. neeraj.agarwal@hci.utah.edu.

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI CORNELIA M ULRICH · 1986 to 2026
$72.6M
NCI NIH HHS P30 CA042014
6 · The paper itself

Abstract

backgroundImmunotherapy with high-dose interleukin-2 (HD-IL2) results in long-term survival in some metastatic renal cell carcinoma (mRCC) patients but has significant acute toxicities. Biomarkers predicting response to therapy are needed to better select patients most likely to benefit. NLR (absolute neutrophil count (ANC)/absolute lymphocyte count (ALC)) is a prognostic and predicative biomarker in various malignancies. The goal was to determine whether NLR can predict response to HD-IL2 in this setting.

methodsPatients with clear cell mRCC treated with HD-IL2 were identified from an institutional database from 2003-2012. Baseline variables for the assessment of IMDC risk criteria, and neutrophil and lymphocyte count, were collected. Best response criteria were based on RECIST 1.0. Wilcoxon rank-sum test was used to evaluate the association of continuous baseline variables with disease control. NLR was stratified by ≤4 or >4. Progression free survival (PFS) and overall survival (OS) were estimated with the Kaplan-Meier method and Cox proportional hazard models assessed associations of NLR with survival.

resultsIn 71 eligible patients, median NLR in those with an objective response (n = 14, 20%) was 2.3 vs 3.4 in those without (n = 57, 80%, p = 0.02). NLR ≤4 was associated with improved progression free and overall survival. After adjustment for IMDC risk criteria, NLR remained a significant predictor of OS (ANC/ALC ≤4 vs >4, HR 0.41, 95% CI 1.09-5.46, p = 0.03; ANC/ALC continuous variable per unit change in NLR, HR 1.08, 95% CI 1.01-1.14, p = 0.03).

conclusionsIn this discovery set, NLR predicts overall survival in patients treated with HD-IL2 in mRCC, and may allow better patient selection in this setting. Data needs validation in an independent cohort.

Indexed as

LymphocytesNeutrophilsAntineoplastic AgentsBiomarkersCarcinoma, Renal CellCohort StudiesFemaleHumansInterleukin-2Kidney NeoplasmsLeukocyte CountMaleMiddle AgedPredictive Value of TestsRetrospective StudiesTreatment OutcomeAntineoplastic AgentsBiomarkersInterleukin-2High dose interleukin-2Neutrophil lymphocyte ratioRenal cell carcinoma

Identifiers

PMID28056941
PMCPMC5217571

What OpenQuestion holds

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LicenceCC BY
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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.