Practical recommendations to combine small-molecule inhibitors and direct oral anticoagulants in patients with nonsmall cell lung cancer

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Serval ID
serval:BIB_947C3642CB1E
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Practical recommendations to combine small-molecule inhibitors and direct oral anticoagulants in patients with nonsmall cell lung cancer
Journal
Eur Respir Rev
Author(s)
Otten L. S., Piet B., van den Heuvel M. M., Marzolini C., van Geel Rmjm, Gulikers J. L., Burger D. M., Leentjens J., Ter Heine R.
ISSN
1600-0617 (Electronic)
0905-9180 (Print)
ISSN-L
0905-9180
Publication state
Published
Issued date
2022
Peer-reviewed
Oui
Volume
31
Number
164
Language
english
Notes
Otten, Leila S
Piet, Berber
van den Heuvel, Michel M
Marzolini, Catia
van Geel, Robin M J M
Gulikers, Judith L
Burger, David M
Leentjens, Jenneke
Ter Heine, Rob
eng
Review
England
Eur Respir Rev. 2022 Jun 14;31(164):220004. doi: 10.1183/16000617.0004-2022. Print 2022 Jun 30.
Abstract
BACKGROUND: The risk for thromboembolisms in nonsmall cell lung cancer (NSCLC) patients is increased and often requires treatment or prophylaxis with direct oral anticoagulants (DOACs). Small-molecule inhibitors (SMIs) to treat NSCLC may cause relevant drug-drug interactions (DDIs) with DOACs. Guidance on how to combine these drugs is lacking, leaving patients at risk of clotting or bleeding. Here, we give practical recommendations to manage these DDIs. METHODS: For all DOACs and SMIs approved in Europe and the USA up to December 2021, a literature review was executed and reviews by the US Food and Drug Administration and European Medicines Agency were analysed for information on DDIs. A DDI potency classification for DOACs was composed and brought together with DDI characteristics of each SMI, resulting in recommendations for each combination. RESULTS: Half of the combinations result in relevant DDIs, requiring an intervention to prevent ineffective or toxic treatment with DOACs. These actions include dose adjustments, separation of administration or switching between anticoagulant therapies. Combinations of SMIs with edoxaban never cause relevant DDIs, compared to more than half of combinations with other DOACs and even increasing to almost all combinations with rivaroxaban. CONCLUSIONS: Combinations of SMIs and DOACs often result in relevant DDIs that can be prevented by adjusting the DOAC dosage, separation of administration or switching between anticoagulants.
Keywords
Administration, Oral, Anticoagulants, *Carcinoma, Non-Small-Cell Lung/drug therapy, Humans, *Lung Neoplasms/drug therapy, Rivaroxaban/adverse effects
Pubmed
Create date
25/08/2023 6:17
Last modification date
25/01/2024 8:40
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