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People with blood clots caused by cancer who took full dose of apixaban for 6 months and then switched to a low dose of apixaban did not have more recurrent blood clots than people who continued to take full dose apixaban.
However, they also did not have fewer major bleeds or clinically relevant nonmajor bleeds than people who continued to take full dose apixaban. Minor bleeds were not recorded.
Understanding the problem
Some people who do not have cancer and take apixaban (Eliquis®) for a blood clot may be given the option of taking a low dose of apixaban (2.5 mg twice a day) after 6 months of treatment or continuing with the full dose (5 mg twice a day). Taking a lower dose of apixaban may reduce the risk of bleeding compared to taking the full dose. Both cancer and anticoagulants can cause bleeding that can range from a minor bleed (e.g. nosebleed that last less than 5 minutes) to a major bleed that is severe enough to be considered life-threatening (e.g. bleed into the brain). Clinically relevant nonmajor bleeds are not as serious as major bleeding but still require assessement by a doctor, a medical intervention (e.g. scope), interruption of the medication, or caused discomfort or impairment of activities of daily living. However, cancer can also be a powerful cause of blood clotting which means the low dose of apixaban may not be strong enough to protect people with cancer from having another blood clot.
The researchers wanted to know if people with blood clots due to cancer would have a lower risk of major or clinically relevant non-major bleeding, if they took a low dose of apixaban after 6 to 12 months of treatment compared with people who continued to take full dose apixaban. They also wanted to know if people who took low dose apixaban would have a higher risk of having another blood clot than people who continued to take full dose apixaban.
Who? The study included 360 adults (average age 64 years, 55% female, 53% had PE, 60% had cancer spread to other locations within their body) who had active cancer within the past 6 months and had been treated with full dose apixaban for 6 to 12 months for a blood clot. People who had severe liver disease, were taking other medications that would interact with apixaban or had another reason to take full dose blood thinners (e.g., atrial fibrillation) were excluded.
What? The study compared low dose apixaban with full dose apixaban for 12 months.
Low dose apixaban | vs | Full dose apixaban |
---|---|---|
Apixaban 2.5 mg twice a day | Apixaban 5 mg twice a day |
Low dose apixaban vs full dose apixaban in people who have blood clots due to cancer and have already been treated with full dose apixaban for 6 to 12 months
Outcomes at 12 months | Rate of events with low dose apixaban | Rate of events with full dose apixaban | Results |
---|---|---|---|
Major bleeding plus clinically relevant non-major bleeding | 9 out of 100 people | 12 out of 100 people | No effect* |
Major bleeding | 3 out of 100 people | 2 out of 100 people | No effect* |
Clinically relevant non-major bleeding | 7 out of 100 people | 10 out of 100 people | No effect* |
Recurrent blood clots | 5 out of 100 people | 4 out of 100 people | No effect* |
*Although the rates for the 2 groups look different, the differences were not statistically significant—this means that the difference could simply be due to chance rather than due to the different treatments.
This Evidence Summary is based on the following article:
McBane RD 2nd, Loprinzi CL, Zemla T, et al. Extending venous thromboembolism secondary prevention with apixaban in cancer patients. The EVE trial. J Thromb Haemost. 2024 Jun;22(6):1704-1714. doi: 10.1016/j.jtha.2024.03.011. Epub 2024 Mar 25. PubMed
Lori-Ann Linkins, MD, MSc (Clin Epi), FRCPC
Dr. Linkins is an Associate Professor of Medicine (thrombosis) at McMaster University in Hamilton, Canada. She holds a Masters Degree in Health Research Methodology and is a Deputy Editor with the Health Information Research Unit, McMaster. She is Co-Editor of the ACP Journal Club and Co-lead on the CanVECTOR Knowledge Translation Platform.
Published: Thursday, July 4, 2024
Last Updated: Wednesday, July 10, 2024
Please note that the information contained herein is not to be interpreted as an alternative to medical advice from a professional healthcare provider. If you have any questions about any medical matter, you should consult your professional healthcare providers, and should never delay seeking medical advice, disregard medical advice or discontinue medication based on information provided here.
This Evidence Summary was printed from the CLOT+ website on 2025/03/30. To view other Evidence Summaries or to register to receive email notifications about new Evidence Summaries, please visit us at https://plus.mcmaster.ca/ClotPlus/Articles/EvidenceSummaries |
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