Evidence map›Paper›PMID 36611408›Full record

ArticleDiagnostics (Basel, Switzerland)2022

NCR, an Inflammation and Nutrition Related Blood-Based Marker in Colon Cancer Patients: A New Promising Biomarker to Predict Outcome.

Melanie Langheinrich, Alexander Reinhard Siebenhüner, Justus Baecker, Maximilian Miragall, Felix Wiesmüller, Vera Schellerer, Susanne Merkel, Maximilian Brunner, Christian Krautz, Klaus Weber and 2 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 6 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

12 authors at 3 institutions in 2 countries.

Melanie LangheinrichDepartment of Surgery, University Hospital of Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-0120-9135
Alexander Reinhard SiebenhünerDepartment of Gastroenterology and Hepatology, University Hospital Zurich and University Zurich, 8006 Zurich, Switzerland.ORCID 0000-0002-5404-2383
Justus BaeckerDepartment of Surgery, University Hospital of Greifswald, 17475 Greifswald, Germany.
Maximilian MiragallDepartment of Surgery, University Hospital of Erlangen, 91054 Erlangen, Germany.
Felix WiesmüllerDepartment of Surgery, University Hospital of Greifswald, 17475 Greifswald, Germany.
Vera SchellererDepartment of Surgery, University Hospital of Erlangen, 91054 Erlangen, Germany.
Susanne MerkelDepartment of Surgery, University Hospital of Erlangen, 91054 Erlangen, Germany.ORCID 0000-0003-2676-9486
Maximilian BrunnerDepartment of Surgery, University Hospital of Erlangen, 91054 Erlangen, Germany.
Christian KrautzDepartment of Surgery, University Hospital of Erlangen, 91054 Erlangen, Germany.ORCID 0000-0002-2537-5824
Klaus WeberDepartment of Surgery, University Hospital of Erlangen, 91054 Erlangen, Germany.
Robert GrützmannDepartment of Surgery, University Hospital of Erlangen, 91054 Erlangen, Germany.
Stephan KerstingDepartment of Surgery, University Hospital of Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-2124-3103
Universitätsklinikum Erlangen · DEUniversitätsmedizin Greifswald · DEUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal carcinoma (CRC) is a heterogeneous disease, and differences in outcomes have been reported among patients diagnosed with the same disease stage. Prognostic and predictive biomarkers provide information for patient risk stratification and guide treatment selection. Although numerous studies have analyzed the effects of systemic inflammatory factors on CRC outcomes, clinical significance remains to be elucidated. In particular, the treatment strategy of colon cancer patients is different from that of rectal cancer due to outcome and recurrence differences. The identification of patients with a poor prognosis who might benefit from intensive treatment approaches is clinically necessary. Methods: This study aimed to evaluate the value of different blood-based markers and assess the significance of our newly developed inflammatory-nutrition-related biomarker (NCR = BMI × albumin/CRP) in patients with colon cancer. A two-stage design was used with 212 patients with colon cancer (CC) in the discovery cohort (n = 159) and in an external validation cohort (n = 53). Results: A lower preoperative NCR level was significantly correlated with a worse prognosis, sidedness, undifferentiated histology, nodal involvement, and advanced UICC stage. We compared the NCR with other established prognostic indices and showed that the NCR is a more reliable indicator of a poor prognosis for patients with CC. Patients with low NCR levels experienced a significantly shorter Overall Survival (OS) than patients with high levels. Multivariate analysis confirmed preoperative NCR levels as an independent predictor for overall survival with a hazard ratio of 3.3 (95% confidence interval 1.628−6.709, p < 0.001). Finally, we confirmed the predictive value of the NCR in an independent validation cohort and confirmed NCR as an independent prognostic factor for OS. Conclusion: Taken together, we discovered a new prognostic index (NCR) based on BMI, albumin, and CRP levels as an independent prognostic predictor of OS in patients with colon cancer. In all UICC stages, our newly developed NCR marker is able to distinguish patients with better and worse prognoses. We, therefore, propose that NCR may serve as a supplement to the TNM staging system to optimize the risk stratification in CC patients towards personalized oncology. In particular, NCR can be used in clinical trials to stratify patients with UICC II and III tumors and help better select patients who might benefit from adjuvant treatment.

Indexed as

biomarkercolon cancercolorectal cancerinflammationnutritionprognosissidednesstumor marker

Identifiers

PMID36611408
PMCPMC9818830
OpenAlexW4313361150

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.