Evidence map›Paper›PMID 42426624›Full record

ArticleBMC gastroenterology2026

Effect of concomitant chemotherapy on edoxaban plasma concentration in patients with colorectal cancer.

Jihyung Song, Kei Kimura, Kozo Kataoka, Hirofumi Ota, Masayoshi Yasui, Taishi Hata, Takashi Daimon, Masataka Ikeda

Abstract read
In one paragraph

Article in BMC gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Jihyung SongDivision of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Mukogawacho 1-1, Nishinomiya City, Hyogo, 663-8501, Japan.
Kei KimuraDivision of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Mukogawacho 1-1, Nishinomiya City, Hyogo, 663-8501, Japan.
Kozo KataokaDivision of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Mukogawacho 1-1, Nishinomiya City, Hyogo, 663-8501, Japan.
Hirofumi OtaDepartment of Gastroenterological Surgery, Ikeda City Hospital, Ikeda City, Japan.
Masayoshi YasuiDepartment of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka City, Japan.
Taishi HataDepartment of Gastroenterological Surgery, Kansai Rosai Hospital, Amagasaki City, Japan.
Takashi DaimonDepartment of Biostatistics, Hyogo Medical University, Nishinomiya City, Japan.
Masataka IkedaDivision of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Mukogawacho 1-1, Nishinomiya City, Hyogo, 663-8501, Japan. ms-ikeda@hyo-med.ac.jp.ORCID http://orcid.org/0000-0001-9602-6659

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDirect oral anticoagulants are a treatment option for cancer-associated venous thromboembolism (VTE). In patients receiving chemotherapy for cancer, there may be pharmacokinetic drug-drug interaction between anti-cancer agents and direct oral anticoagulants. However, there are no data available in patients with colorectal cancer (CRC). In this study, we investigated edoxaban plasma concentration in patients with CRC receiving chemotherapy.

methodsThe study included patients with unresectable or metastatic CRC undergoing systemic chemotherapy and simultaneously receiving anticoagulant therapy with edoxaban for VTE or atrial fibrillation. Blood sampling was performed prior to chemotherapy and after 24 h and 48 h depending on the chemotherapy regimen.

resultsData of 21 and 26 patients were analyzed for edoxaban plasma concentration and safety, respectively. Edoxaban plasma concentration was not statistically different before and after 24 h and 48 h between patients receiving treatment with a chemotherapy regimen, cytotoxic drug, and a molecular targeted drug. One patient had major bleeding requiring transfusion; however, edoxaban plasma concentration was not elevated before and 24 h after chemotherapy (19.98 and 9.63 ng/ml, respectively).

conclusionIn patients with CRC, edoxaban plasma concentration did not change after chemotherapy, implying that drug-drug interaction between edoxaban and anti-cancer agents was minimal.

Indexed as

Antineoplastic AgentsColorectal NeoplasmsFactor Xa InhibitorsPyridinesThiazolesVenous ThromboembolismAgedAged, 80 and overAtrial FibrillationDrug InteractionsFemaleHumansMaleMiddle AgedAntineoplastic AgentsedoxabanFactor Xa InhibitorsPyridinesThiazolesChemotherapyColorectal cancerDOACDrug–drug interactionEdoxaban

Identifiers

PMID42426624
PMCPMC13632323

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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.