Evidence map›Paper›PMID 38357476›Full record

ArticleOncology letters2024

Inflammation‑based prognostic markers of metastatic pancreatic cancer using real‑world data in Japan: The Tokushukai REAl‑world Data (TREAD) project.

Rai Shimoyama, Yoshinori Imamura, Kiyoaki Uryu, Takahiro Mase, Megumi Shiragami, Yoshiaki Fujimura, Maki Hayashi, Megu Ohtaki, Keiko Ohtani, Nobuaki Shinozaki and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 5 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

11 authors at 5 institutions in 1 country.

Rai ShimoyamaDepartment of General Surgery, Shonan Kamakura General Hospital, Kamakura, Kanagawa 247-8533, Japan.
Yoshinori ImamuraDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Hyogo 650-0017, Japan.
Kiyoaki UryuDepartment of Medical Oncology, Yao Tokushukai General Hospital, Osaka 581-0011, Japan.
Takahiro MaseDepartment of Breast Surgery, Ogaki Tokushukai Hospital, Ogaki, Gifu 503-0015, Japan.
Megumi ShiragamiTokushukai Information System, Inc., Osaka 530-0001, Japan.
Yoshiaki FujimuraTokushukai Information System, Inc., Osaka 530-0001, Japan.
Maki HayashiMirai Iryo Research Center Inc., Tokyo 102-0074, Japan.
Megu OhtakideCult Co., Ltd., Hatsukaichi, Hiroshima 739-0413, Japan.
Keiko OhtanideCult Co., Ltd., Hatsukaichi, Hiroshima 739-0413, Japan.
Nobuaki ShinozakiDepartment of General Surgery, Shonan Kamakura General Hospital, Kamakura, Kanagawa 247-8533, Japan.
Hironobu MinamiDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Hyogo 650-0017, Japan.
Fukuoka Tokushukai Hospital · JPKobe University · JPShonan Kamakura General Hospital · JPMirai Hospital · JPYao Tokushukai General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation-based prognostic markers based on a combination of blood-based parameters, including the modified Glasgow prognostic score (mGPS), have been associated with clinical outcomes in patients with various types of cancer. The present study aimed to evaluate and compare the accuracy of these previously reported markers in patients with metastatic pancreatic cancer receiving first-line chemotherapy. A total of 846 patients were identified between April 2010 and March 2020 as part of a nationwide real-world study from 46 Tokushukai medical group hospitals in Japan. Blood laboratory data collected within 14 days of starting first-line chemotherapy assessed 17 inflammation-based prognostic markers. Information from patients with no missing data was used to compare the accuracy and performance of the inflammation-based prognostic markers. A total of 487 patients were eligible for this supplemental analysis. The 17 inflammation-based markers demonstrated significant prognostic value. Among them, the concordance rate with overall survival (OS) was highest for mGPS. The median OS time of patients with mGPS 0, 1 and 2 was 8.2, 6.0 and 2.9 months, respectively. Compared with mGPS 0, mGPS 1 and 2 showed hazard ratios of 1.39 (95% confidence interval, 1.07-1.81) and 2.63 (2.00-3.45), respectively. The present real-world data analysis showed that various previously reported inflammation-based markers had significant prognostic value in patients with metastatic pancreatic cancer. Among these markers, the mGPS demonstrated the highest level of accuracy. This trial has been registered in the University Hospital Medical Information Network Clinical Trials Registry as UMIN000050590 on April 1, 2023.

Indexed as

inflammation-based prognostic markersmetastatic pancreatic cancermGPSOSreal-world data

Identifiers

PMID38357476
PMCPMC10865166
OpenAlexW4391387757

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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.