Effectiveness and safety of anticoagulants among venous thromboembolism cancer patients with and without brain cancer.


Journal

Thrombosis research
ISSN: 1879-2472
Titre abrégé: Thromb Res
Pays: United States
ID NLM: 0326377

Informations de publication

Date de publication:
06 2023
Historique:
received: 09 12 2022
revised: 29 03 2023
accepted: 10 04 2023
medline: 23 5 2023
pubmed: 6 5 2023
entrez: 5 5 2023
Statut: ppublish

Résumé

Patients with brain cancer are at a high risk of developing venous thromboembolism (VTE) and are underrepresented in clinical trials. This study compared the risk of recurrent VTE (rVTE), major bleeding (MB), and clinically relevant non-major bleeding (CRNMB) among VTE cancer patients initiating apixaban, low molecular weight heparin (LMWH), or warfarin stratified by patients with brain vs other cancer types. Active cancer patients initiating apixaban, LMWH, or warfarin within 30 days after VTE diagnosis were identified from 4 US commercial and the Medicare databases. Inverse probability of treatment weights (IPTW) was used to balance patient characteristics. Cox proportional hazards models were used to evaluate the interaction between brain cancer status and treatment on outcomes (rVTE, MB, and CRNMB), with a p-value <0.1 indicating a significant interaction. Of 30,586 patients with active cancer (5 % had brain cancer), apixaban (vs. LMWH and warfarin) was associated with lower risk of rVTE, MB, and CRNMB. Generally, no significant interactions (P > 0.1) were found between brain cancer status and anticoagulant treatment across outcomes. The exception was MB for apixaban [vs LMWH (p-value for interaction = 0.091)] with a higher reduction among those with brain cancer (HR = 0.32) than those with (HR = 0.72) other cancer. Among VTE patients with all types of cancer, apixaban (vs LMWH and warfarin) was associated with a lower risk of rVTE, MB, and CRNMB. In general, anticoagulant treatment effects were not significantly different between VTE patients with brain cancer and those with other cancer.

Identifiants

pubmed: 37146438
pii: S0049-3848(23)00101-9
doi: 10.1016/j.thromres.2023.04.009
pii:
doi:

Substances chimiques

Anticoagulants 0
Warfarin 5Q7ZVV76EI
Heparin, Low-Molecular-Weight 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117-126

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest AC received research support from Pfizer Inc. and Bristol-Myers Squibb Company. VN, RB and SS were paid employees of STATinMED at the time of the study; STATinMED is a paid consultant to Pfizer, Inc. and Bristol-Myers Squibb Company in connection with the development of this manuscript. AD is a paid employee of Bristol-Myers Squibb Company. DMH, TA, and XL are paid employees of Pfizer, Inc.

Auteurs

Alexander Cohen (A)

Department of Hematological Medicine, Guy's & St Thomas' NHS Foundation Trust, King's College London, Westminster Bridge Road, London, UK. Electronic address: alexander.cohen@kcl.ac.uk.

Virginia Noxon (V)

STATinMED, LLC, Dallas, TX, USA.

Amol Dhamane (A)

Bristol Myers Squibb Company, Lawrenceville, NJ, USA.

Robert Bruette (R)

STATinMED, LLC, Dallas, TX, USA.

Shrushti Shah (S)

STATinMED, LLC, Dallas, TX, USA.

Dionne M Hines (DM)

Pfizer Inc., New York, NY, USA.

Tamuno Alfred (T)

Pfizer Inc., New York, NY, USA.

Xuemei Luo (X)

Pfizer Inc., Groton, CT, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH