Evidence map›Paper›PMID 28685065›Full record

ArticleBiomedical reports2017

Increased neutrophil-to-lymphocyte ratio is a novel marker for nutrition, inflammation and chemotherapy outcome in patients with locally advanced and metastatic esophageal squamous cell carcinoma.

Yu Sato, Kenji Gonda, Maiko Harada, Yuki Tanisaka, Shin Arai, Yumi Mashimo, Hirotoshi Iwano, Hiroshi Sato, Shomei Ryozawa, Takao Takahashi and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Biomedical reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 31 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 4 institutions in 1 country.

Yu SatoDepartment of Surgery, Toho University Sakura Medical Center, Sakura, Chiba 285-8741, Japan.
Kenji GondaDepartment of Gastroenterological Oncology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Maiko HaradaDepartment of Gastroenterology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Yuki TanisakaDepartment of Gastroenterology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Shin AraiDepartment of Gastroenterology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Yumi MashimoDepartment of Gastroenterology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Hirotoshi IwanoDepartment of Gastroenterology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Hiroshi SatoDepartment of Surgery, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Shomei RyozawaDepartment of Gastroenterology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Takao TakahashiDepartment of Palliative Medicine, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Shinichi SakuramotoDepartment of Surgery, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Masahiko ShibataDepartment of Advanced Cancer Immunotherapy, Fukushima Medical University, Fukushima, Fukushima 960-1259, Japan.
Saitama Medical University · JPSaitama International Medical Center · JPFukushima Medical University · JPToho University Medical Center Sakura Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esophageal squamous cell carcinoma (ESCC) is one of the most common types of cancer, and its progression is strongly influenced by the presence of inflammation. Recently, there has been growing interest in the host inflammatory response, and increasing evidence has indicated that the neutrophil-to-lymphocyte ratio (NLR), a useful marker of systemic inflammation, may be an effective prognostic indicator in various types of malignant diseases. In the present study, 260 patients with ESCC were enrolled, including 110 who received chemoradiation therapy (CRT) involving irradiation and chemotherapy of 5-fluorouracil and cisplatin, and 150 received chemotherapy using 5-fluorouracil and cisplatin (FP). The patients of each group were both divided into two groups according to their NLR: High NLR (NLR>3.0) and low NLR (NLR≤3.0). Serum levels of prealbumin and retinol binding protein, which are nutritional parameters, were both significantly inversely correlated with NLR in patients treated with CRT, and patients treated with FP. Levels of CRP, a marker of inflammation, were significantly correlated with NLR, and stimulation indices, markers of immune reactions, were inversely correlated with NLR in both of CRT patients and FP patients. In patients treated with CRT, a partial response was significantly higher in patients with a low NLR and with progressive disease compared to those with a high NLR. In patients treated with FP, a partial response was also significantly higher in patients with a low NLR and with progressive disease compared to those with a high NLR. The overall survival of patients with CRT and FP were both significantly worse in patients with a high NLR than in those with a low NLR. NLR may serve as a useful marker of the tumor response, immune suppression, malnutrition and prognosis upon CRT or FP in patients with locally advanced or metastatic ESCC.

Indexed as

esophageal squamous cell carcinomainflammationneutrophil-to-lymphocyte rationutrition

Identifiers

PMID28685065
PMCPMC5492691
OpenAlexW2624171002

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.