Evidence map›Paper›PMID 30680213›Full record

ArticleMolecular and clinical oncology2019

Elevated IL-6/IL-1Ra ratio as a prognostic biomarker of poor chemotherapy efficacy in Chinese patients with metastatic NSCLC, validated in a Caucasian patient cohort.

Fang Liu, Benoît Sansas, Xavier Préville, Romain Gineste, Jialei Wang, Hui Yu, Xia Meng, Romain Micol, Luc Barraud

Abstract read
In one paragraph

Article in Molecular and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

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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

9 authors.

Fang LiuTransgene Biopharmaceutical Technology Co. Ltd., Shanghai 201315, P.R. China.
Benoît SansasResearch and Innovation Department, Transgene S.A., 67405 Illkirch Graffenstaden, France.
Xavier PrévilleResearch and Innovation Department, Transgene S.A., 67405 Illkirch Graffenstaden, France.
Romain GinesteTransgene Biopharmaceutical Technology Co. Ltd., Shanghai 201315, P.R. China.
Jialei WangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 201315, P.R. China.
Hui YuDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 201315, P.R. China.
Xia MengTransgene Biopharmaceutical Technology Co. Ltd., Shanghai 201315, P.R. China.
Romain MicolResearch and Innovation Department, Transgene S.A., 67405 Illkirch Graffenstaden, France.
Luc BarraudResearch and Innovation Department, Transgene S.A., 67405 Illkirch Graffenstaden, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment options for advanced (stage IV) non-small cell lung cancer (NSCLC) at diagnosis remain disappointing. The development of immunotherapeutic drugs may represent a promising alternative approach to the treatment of late-stage cancer at diagnosis. These current paradigms in cancer treatment highlight the need for new biomarkers related to the immune status of the patients and/or the tumor microenvironment, for immune as well as chemotherapeutic treatment options. The aim of the present study was to analyze soluble immune factors in patients with lung cancer treated with chemotherapy to identify prognostic biomarkers. For this purpose, the data obtained from two cohorts of patients from different clinical trials were analyzed: A Chinese patient cohort to identify potential prognostic biomarkers, and a validation cohort comprising patients with a similar clinical stage from a clinical trial in Europe. Analyses of soluble markers for inflammation and immune status were performed by standard assays and multiplex Luminex assays. Differences in overall survival (OS) and progression-free survival (PFS) were evaluated with the log-rank test and robustness was evaluated with the resampling approach. In the Chinese cohort, four prognostic biomarkers of poor response to chemotherapy were identified, which had a significant impact on OS and PFS. It was confirmed in the Caucasian validation cohort that an increased value of the interleukin (IL)-6/IL-1Ra cytokine ratio at inclusion was correlated with significantly shorter OS and PFS, whereas no other biomarkers were found to be significant. The IL-6/IL-1Ra ratio reflects the imbalance between pro- and anti-inflammatory status in the plasma of patients and may be associated with tumor inflammatory status and the therapeutic outcome. The present study highlights the identification of the IL-6/IL-1Ra ratio as a biomarker of poor prognosis in terms of response to chemotherapy in two independent clinical studies.

Indexed as

cytokinesimmunophenotypingnon-small cell lung cancerprognostic factor

Identifiers

PMID30680213
PMCPMC6327210

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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.