Evidence map›Paper›PMID 40241057›Full record

ArticleThrombosis journal2025

Anticoagulant effects of edoxaban in cancer and noncancer patients with venous thromboembolism.

Masashi Yoshida, Kentaro Ejiri, Naoaki Matsuo, Takanori Naito, Kazuhiro Kuroda, Koji Tokioka, Kunihiko Hatanaka, Ryohei Fujimoto, Hidenaru Yamaoka, Yutaka Kajikawa and 11 more

Abstract read
In one paragraph

Article in Thrombosis journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

21 authors.

Masashi YoshidaDepartment of Cardiovascular Medicine, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Okayama, 700- 8558, Japan. yoshid-m@cc.okayama-u.ac.jp.
Kentaro EjiriDepartment of Cardiovascular Medicine, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Okayama, 700- 8558, Japan.
Naoaki MatsuoDepartment of General Internal Medicine 3, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama, 701-0192, Japan.
Takanori NaitoDepartment of Cardiovascular Medicine, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Okayama, 700- 8558, Japan.
Kazuhiro KurodaDepartment of Cardiovascular Medicine, Japanese Red Cross Okayama Hospital, 2-1-1 Aoe, Kita-ku, Okayama, Okayama, 700-8607, Japan.
Koji TokiokaDepartment of Cardiovascular Medicine, Okayama City Hospital, 3-20-1 Kitanagaseomote-cho, Kita-ku, Okayama, Okayama, 700-8557, Japan.
Kunihiko HatanakaDepartment of Cardiovascular Medicine, Japanese Red Cross Society Himeji Hospital, 1-12-1 Shimotemo, Himeji, Hyougo, 670-8540, Japan.
Ryohei FujimotoDepartment of Cardiovascular Medicine, Tsuyama Chuo Hospital, 1756 Kawasaki, Tsuyama, Okayama, 708-0841, Japan.
Hidenaru YamaokaDepartment of Cardiovascular Medicine, Okayama Rosai Hospital, 1-10-25 Chikkoumidorimachi, Nimani-ku, Okayama, Okayama, 702-8055, Japan.
Yutaka KajikawaDepartment of Cardiovascular Medicine, NHO Fukuyama Medical Center, 4-14-17 Okinogami- cho, Fukuyama, Hiroshima, 720-8520, Japan.
Kazuki SurugaDepartment of Cardiovascular Medicine, Okayama Medical Center, 1711-1 Tamasu, Kita-ku, Okayama, Okayama, 701-1192, Japan.
Hiroki SugiyamaDepartment of Cardiovascular Medicine, Okayama Saiseikai General Hospital, 2-25 Kokutai- cho, Kita-ku, Okayama, Okayama, 700-8511, Japan.
Tsuyoshi MiyajiHosogi Hospital, 37 Daizen-cho, Kochi, Kochi, 780-8535, Japan.
Yoshimasa MorimotoDepartment of Cardiovascular Medicine, Fukuyama City Hospital, 5-23-1 Zaou-cho, Fukuyama, Hiroshima, 721-8511, Japan.
Nobuhiro OkamuraOkamura Isshindow Hospital, 2-1-7 Saidaijiminami, Higashi-ku, Okayama, Okayama, 704-8117, Japan.
Toshihiro SarashinaKuroda Clinic, 2-8-35 Kanda-cho, Kita-ku, Okayama, Okayama, 700-0935, Japan.
Satoshi AkagiDepartment of Cardiovascular Medicine, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Okayama, 700- 8558, Japan.
Toru MiyoshiDepartment of Cardiovascular Medicine, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Okayama, 700- 8558, Japan.
Kazufumi NakamuraDepartment of Cardiovascular Medicine, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Okayama, 700- 8558, Japan.
Hiroshi ItoDepartment of General Internal Medicine 3, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama, 701-0192, Japan.
Shinsuke YuasaDepartment of Cardiovascular Medicine, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, Okayama, 700- 8558, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEdoxaban, a direct oral anticoagulant (DOAC), is a first-line treatment for venous thromboembolism (VTE) and the suppression of VTE recurrence. In patients with cancer, however, recurrent VTE after DOAC treatment may be more common than in noncancer patients. To evaluate our hypothesis that the anticoagulation effect of edoxaban is lower in VTE patients with cancer than in noncancer patients.

methodsThis study was a prospective, multicenter, observational study including patients treated with edoxaban for VTE in Japan. The primary outcome was the difference in the prothrombin time (PT), activated partial thromboplastin time (APTT), and D-dimer level at 5 h after initial edoxaban administration between the cancer and noncancer groups. An additional outcome was the longitudinal change in PT and APTT from 5 h to overnight after edoxaban administration. The incidence of adverse events was further investigated.

resultsPT and APTT at 5 h after initial edoxaban administration were not significantly different between the cancer (n = 84) and noncancer groups (n = 138) (e.g., log-transformed APTT 3.55 vs. 3.55, p = 0.45). However, D-dimer in the cancer groups was significantly greater than that in the noncancer groups (log-transformed 1.83 vs. 1.79, p = 0.009). PT and APTT significantly decreased from 5 h to overnight after edoxaban, but a similar pattern was observed in each group. All adverse events after edoxaban administration were also similar between patients with cancer and noncancer.

conclusionPT and APTT after edoxaban administration were similar between VTE patients with cancer and noncancer groups, suggesting that edoxaban has anticoagulation effects on cancer-associated VTE similar to those of noncancer patients.

trial registrationUMIN000041973; Registration Date: 2020.10.5.

Indexed as

Anticoagulation effectsCancerFactor Xa inhibitorsVenous thromboembolism

Identifiers

PMID40241057
PMCPMC12001618

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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.