Apixaban for the Prevention of Venous Thromboembolism in Cancer Patients

Cancer Clinical Trial

— AVERT  

Official title:

Apixaban for the Prevention of Venous Thromboembolism in High-Risk Ambulatory Cancer Patients: A Randomized Placebo-Controlled, Double-Blind Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02048865
• Other study ID #: OHSN-20130563-01H
• Secondary ID: CV185-245
• Status: Completed
• Phase: Phase 2
• Start date: March 24, 2014
• Est. completion date: October 19, 2018

Study information

• Verified date: November 2018
• Source: Ottawa Hospital Research Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cancer patients have an increased risk of developing blood clots in the veins compared to non-cancer patients. Cancer patients who develop blood clots can lead to reduced life expectancy, delayed cancer treatment, and decreased quality of life. Prevention is the most effective way to decrease the complications associated with blood clots in the veins. Although previous clinical trials have shown some benefit on the use of medication to prevent blood clots in the veins in ambulatory cancer patients, these studies have been inconclusive in demonstrating that existing blood thinners significantly reduce the rate of blood clots in cancer patients. One possible explanation relates to the fact that these studies have included a large proportion of cancer patients who are a low risk of developing blood clots in the veins. We are proposing to identify cancer patients who are at a high risk of developing blood clots by using a validated tool at the time of their cancer diagnosis. The identified high risk cancer patients will be asked to participate in a trial to test the safety and efficacy of a new oral medication that has been used to prevent blood clots in patients undergoing surgery. We are enrolling 574 patients in 7 Canadian centers (Ottawa, Halifax, Montreal, Vancouver, Sault Ste. Marie, Toronto and Hamilton). 287 patients will receive the study drug and 287 will receive an inactive substance. Analysis will be performed to assess the safety and the superiority of the study drug.

Description:

Patients holding a malignancy have a 7 to 28-fold higher risk for venous thromboembolism (VTE) than non-cancer patients(1). Since most cancer patients are currently treated in the outpatient setting, an acute episode of VTE has important implications on their care due to its effects on reduced life expectancy, high rates of VTE recurrence, therapeutic failures, delays in chemotherapy and the risk of bleeding during anticoagulation.

The best treatment of an acute episode of VTE is its prevention (thromboprophylaxis). Although previous clinical trials have shown some benefit on the use of thromboprophylaxis in ambulatory cancer patients, these studies have been inconclusive to convincingly demonstrate that existing anticoagulants significantly reduce the rate of VTE in cancer patients. Possible explanations are related to the fact that these studies have included a large number of cancer patients whose risk for VTE has been low and in consequence, the benefit of anticoagulation has become diluted by the large proportion of low risk cancer patients.

To increase the success of thromboprophylaxis in cancer outpatients, we propose, first, to include validated methods for predicting the risk of VTE at the time of cancer diagnosis(2, 3). This strategy will facilitate to identify cancer patients at high-risk for VTE and then, optimize the risk-to benefit ratio with anticoagulation. Second, to assess safety and efficacy of new oral anticoagulants in cancer patients as they represent an attractive alternative for an extended use of thromboprophylaxis. As a choice, new oral agents can be administered in fixed doses, do not require laboratory monitoring, have minimal interaction with additional drugs and provide a pain free alternative in patients who require injections.

Reference List

1. Blood Coagul Fibrinolysis 2011. Blood Coagul Fibrinolysis 2011;22:86-91.

2. Blood 2010. Blood 2010;116:5377-5382.

3. Blood 2008. Blood 2008;111:4902-4907.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 575
• Est. completion date: October 19, 2018
• Est. primary completion date: October 10, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• A newly diagnosed cancer site or progression of the malignant disease after complete or partial remission.

• Initiating a new course of chemotherapy with a minimum intent of 3 months therapy

• A VTE risk stratification score of = 2, according to the scoring method

• Age 18 years old or older

• Provide written informed consent

Exclusion Criteria:

• Lesions or conditions at increased risk of clinically significant bleeding (eg. active peptic ulcer disease)

• Objectively confirmed substantial liver insufficiency as defined by clinical manifestations of ascites, cirrhosis, encephalopathy and/or jaundice and/or biochemical abnormalities in liver function tests including hypoalbuminemia (< 3.5 gr/dL), elevated levels of total bilirubin (> 25 umol/L), elevated liver transaminases (2 times the upper limit of normal) and/or biochemical diagnosis of biliary tract obstruction (elevated levels of gamma-glutamyl transferase and alkaline phosphatase, 3 times the upper limit of normal). *

• Diagnosis of basal cell or squamous cell carcinoma of the skin or acute leukemia or myelodysplastic syndrome**

• Planned stem cell transplant

• Life expectancy less than 6 months

• Acute or chronic renal insufficiency with glomerular filtration rate (GFR) < 30 ml/min calculated by the Cockroft and Gault formula.

• Pregnancy***

• Continuous anticoagulation with vitamin K antagonists, low-molecular-weight heparin (LMWH), or other oral anticoagulants

• Weight < 40 Kg

• Platelet count < 50 x 109/L

• Known allergies to ingredients contained in apixaban

• Use of any contraindicated medications with apixaban

Related Conditions & MeSH terms

• Cancer
• Thromboembolism
• Venous Thromboembolism

Intervention

Drug:
• Apixaban
Apixaban 2.5 mg tablets BID for 6 months
• Placebo drug
placebo drug 2.5mg BID for 6 months

Locations

Country	Name	City	State
Canada	Royal Victoria Regional Health Centre (RVH)	Barrie	Ontario
Canada	William Osler Health System -Brampton	Brampton	Ontario
Canada	Centre intégré de santé et de services sociaux de l'Outaouais - Gatineau	Gatineau	Quebec
Canada	Capital District Health Authority	Halifax	Nova Scotia
Canada	Juravinski Hospital & Cancer Centre	Hamilton	Ontario
Canada	Kingston General Hospital	Kingston	Ontario
Canada	London Health Sciences Center	London	Ontario
Canada	Jewish General Hospital	Montreal	Quebec
Canada	Lakeridge Health -Oshawa	Oshawa	Ontario
Canada	Ottawa Hospital-General Campus	Ottawa	Ontario
Canada	Centre intégré de santé et de services sociaux du Bas St Laurent -Rimouski	Rimouski	Quebec
Canada	Sault Area Hospital	Sault Ste. Marie	Ontario
Canada	Markham Stouffville Hospital	Toronto	Ontario
Canada	Vancouver General Hospital	Vancouver	British Columbia

Sponsors (3)

Lead Sponsor	Collaborator
Ottawa Hospital Research Institute	Bristol-Myers Squibb, Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	first episode of objectively documented, symptomatic or asymptomatic VTE (DVT and/or PE)		7 months
Secondary	Rate of adverse events	rate of clinical overt bleeding( major and minor bleeding) and death within the study period	7 months