Evidence map›Paper›PMID 33841940›Full record

ArticleJournal of thoracic disease2021

High serum C-reactive protein levels predict survival in patients with treated advanced lung adenocarcinoma.

Takamasa Hotta, Kazuhisa Nakashima, Kojiro Hata, Yukari Tsubata, Takeshi Isobe

Open access · diamondAbstract read
In one paragraph

Article in Journal of thoracic disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Takamasa HottaDepartment of Internal Medicine, Division of Medical Oncology & Respiratory Medicine, Shimane University, Shimane, Japan.
Kazuhisa NakashimaDepartment of Internal Medicine, Division of Medical Oncology & Respiratory Medicine, Shimane University, Shimane, Japan.
Kojiro HataDepartment of Internal Medicine, Division of Medical Oncology & Respiratory Medicine, Shimane University, Shimane, Japan.
Yukari TsubataDepartment of Internal Medicine, Division of Medical Oncology & Respiratory Medicine, Shimane University, Shimane, Japan.
Takeshi IsobeDepartment of Internal Medicine, Division of Medical Oncology & Respiratory Medicine, Shimane University, Shimane, Japan.
Shimane University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prognosis of non-small cell lung cancer (NSCLC) varies greatly depending on whether or not it can receive molecular-targeted drug treatment including epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs). We investigated the clinical utility of C-reactive protein (CRP) levels measured at the time of diagnosis in EGFR-mutant and wild-type NSCLC patients who had undergone first-line therapy.

methodsSerum CRP levels were analyzed in 213 patients, of whom 89 patients had advanced EGFR-mutated NSCLC who underwent first-line EGFR-TKI treatment. We used Cox proportional hazards models to study the relationship between CRP and overall survival (OS). CRP cutoff values were obtained from the receiver operating characteristic curve.

resultsMean serum CRP level in treated NSCLC patients were not significantly different in patients with or without EGFR mutations. The optimal CRP cutoff values were 8.1 mg/L for EGFR-mutated NSCLC and 16.7 mg/L for EGFR-wild NSCLC. Based on multivariate analysis, high CRP level (EGFR-mutated, HR: 2.479, 95% CI: 1.331-4.619, P=0.004; EGFR-wild, HR: 3.625, 95% CI: 2.149-6.116, P<0.001) was a significant and independent negative prognostic factor for OS in patients with or without EGFR mutations.

conclusionsHigh CRP levels predicted a lack of response to treatment in patients with advanced lung adenocarcinoma with or without EGFR mutations. Thus, the CRP level is a good and easy to use prognostic factor and objective indicator for clinical practice.

Indexed as

advanced non-small cell lung cancer (advanced NSCLC)BiomarkerC-reactive protein concentration (CRP concentration)epidermal growth factor receptor tyrosine kinase inhibitor (EGFR TKI)

Identifiers

PMID33841940
PMCPMC8024849
OpenAlexW3134349103

What OpenQuestion holds

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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.