Evidence map›Paper›PMID 39931081›Full record

ArticleFrontiers in oncology2025

Effect of drug interactions with apixaban on clinical outcomes in cancer patients with venous thromboembolism.

Marte Svalastoga, Trine-Lise Larsen, Jorunn Brekke, Tone Enden, Hege Frøen, Herish Garresori, Eva Marie Jacobsen, Alina Carmen Porojnicu, Anne Hansen Ree, Dag Torfoss and 5 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 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

15 authors.

Marte SvalastogaInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Trine-Lise LarsenInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Jorunn BrekkeDepartment of Oncology, Haukeland University Hospital, Bergen, Norway.
Tone EndenDepartment of Radiology, Oslo University Hospital, Oslo, Norway.
Hege FrøenDepartment of Medicine, Baerum Hospital, Vestre Viken Hospital Trust, Drammen, Norway.
Herish GarresoriDepartment of Oncology, Stavanger University Hospital, Stavanger, Norway.
Eva Marie JacobsenDepartment of Haematology, Oslo University Hospital, Oslo, Norway.
Alina Carmen PorojnicuDepartment of Oncology, Drammen Hospital, Vestre Viken Hospital Trust, Drammen, Norway.
Anne Hansen ReeInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Dag TorfossDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Elin Osvik VelleDepartment of Medicine, Volda Hospital, Møre and Romsdal Hospital Trust Volda, Volda, Norway.
Hilde Skuterud WikDepartment of Haematology, Oslo University Hospital, Oslo, Norway.
Waleed GhanimaInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Per Morten SandsetInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Anders Erik Astrup DahmInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: It is unclear how drug-interaction with apixaban influences recurrent venous thromboembolism (VTE) and bleedings in cancer patients. Methods: A Results: 298 patients were divided into groups based on whether they used no interacting drugs (controls, n=74), drugs increasing bleeding risk (n=55), drugs increasing thrombosis risk (n=8), or both (n=161). Odds ratios (OR) were calculated for recurrent VTE, clinically relevant non-major bleeding (CRNMB), and major bleeding during the 36-month follow-up period. Each patient took a median of 13 different drugs over the study period. 67% of the patients used drugs expected to both increase bleeding and thrombosis. The use of fluconazole appeared associated with CRNMB (OR 3.6, 95% confidence interval (CI) 0.99-13), but not with major bleeding (OR 0.56, 95% CI 0.06 - 4.8). Non-steroid anti-inflammatory drugs were not associated with CRNMB (OR 1.0, 95% CI 0.25-4.1) or major bleedings (OR 0.72, 95% CI 0.14 - 3.6). Use of antiplatelet therapy was not associated with CRNMB (OR 0.75, 95% CI, 0.22 - 2.58) or major bleeding (OR 0.2, 95% CI, 0.02-1.6). There were no major bleedings in 23 patients using aprepitant nor in the 10 patients taking macrolides. We found no association between drugs and recurrent VTE, except that there were no recurrent VTE in 19 patients using bevacizumab. Conclusions: Despite the high number of drugs taken that could potentially interact with apixaban, none were found to clearly influence clinical outcomes, except that fluconazole may increase the risk of CRNMB.

Indexed as

apixabanbleedingcancerdrug-drug interactionvenous thromboembolism

Identifiers

PMID39931081
PMCPMC11807833

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.