Evidence map›Paper›PMID 41674799›Full record

ArticleCirculation reports2026

Impact of Chemotherapy and Anticancer Agent Type on 30-Day All-Cause In-Hospital Mortality of Venous Thromboembolism Patients With Cancer in Japan.

Takahiro Okada, Tomiko Sunaga, Yoshitaka Iso, Mio Ebato, Tsutomu Toshida, Shuichi Nawata, Hiroshi Suzuki, Mari Kogo

Abstract read
In one paragraph

Article in Circulation reports, 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
–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

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.

Takahiro OkadaDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa Medical University Tokyo Japan.
Tomiko SunagaDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa Medical University Tokyo Japan.
Yoshitaka IsoDivision of Cardiology, Department of Internal Medicine, Showa Medical University Fujigaoka Hospital Yokohama Japan.
Mio EbatoDivision of Cardiology, Department of Internal Medicine, Showa Medical University Fujigaoka Hospital Yokohama Japan.
Tsutomu ToshidaDivision of Cardiology, Department of Internal Medicine, Showa Medical University Fujigaoka Hospital Yokohama Japan.
Shuichi NawataDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa Medical University Tokyo Japan.
Hiroshi SuzukiDivision of Cardiology, Department of Internal Medicine, Showa Medical University Fujigaoka Hospital Yokohama Japan.
Mari KogoDivision of Pharmacotherapeutics, Department of Clinical Pharmacy, School of Pharmacy, Showa Medical University Tokyo Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: To contribute to the treatment and management of venous thromboembolism (VTE) patients with cancer, we used data from the Japanese Registry of All Cardiac and Vascular Diseases and the Diagnosis Procedure Combination database to clarify the impact of chemotherapy on 30-day all-cause in-hospital mortality. Annual changes in oral anticoagulant use were also evaluated. Methods and Results: We identified 106,404 VTE patients who were hospitalized for the management of VTE between 2012 and 2021. The primary outcome was all-cause in-hospital mortality within 30 days after admission for VTE. After adjusting for covariates using propensity score (PS) matching, outcomes were compared between patients with and without chemotherapy. In the PS-matched cohort, subgroup analyses estimated the association between specific anticancer agents or hormone therapy and 30-day all-cause mortality. Mortality was significantly lower in the group with than without chemotherapy group (odds ratio 0.46; P<0.001). However, the analysis revealed no significant association between any anticancer agent or therapy and 30-day mortality. Warfarin use decreased markedly from 100% in 2012 to 7% in 2021, whereas the use of oral direct Factor Xa inhibitors increased significantly (P for trend <0.001). Conclusions: In this study, 30-day mortality was lower in the group with than without chemotherapy group. Among VTE patients with cancer, direct Factor Xa inhibitors appear to be preferred over warfarin due to bleeding risk.

Indexed as

Cardio-oncologyChemotherapyVenous thromboembolism

Identifiers

PMID41674799
PMCPMC12887195

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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.