Reduction to Preventive Doses of Enoxaparin After 3 to 6 Months of Treatment With Blood Thinners for Cancer-associated Blood Clots

NCT02752607 | Terminated

• 1 other identifier: MM-JGH-16-003
• Study Type: observational
• Target: 52
• Locations: 1 country
• Sites: 7

Brief Summary

Background: Venous thromboembolism (VTE), which includes deep vein thrombosis (DVT) and pulmonary embolism (PE), is the third most common cardiovascular disorder after myocardial infarction and stroke. VTE occurs in about 1 person per 1,000 per year, increasing dramatically in patients with cancer to about 25 per 1,000 per year. Among the known risk factors of VTE, cancer is one of the most potent. Patients with cancer have a 7- to 28-fold higher risk for VTE than non-cancer patients. VTE has important implications for the care of cancer patients, including reduced life expectancy, high rates of VTE recurrence both while on and after stopping anticoagulation, the need for chronic anticoagulation with related adverse drug reactions, and delays in cancer therapies. Clinical dilemma: Current clinical guidelines recommend a minimum of 3-6 months of anticoagulation with weight-adjusted low molecular weight heparin (LMWH) in cancer patients with VTE. However, there are no recommendations beyond the initial 6 months of therapy due to the lack of data on extended duration therapy for cancer-associated thrombosis (CAT). This leads to variability in physician practices, with some continuing weight-adjusted LMWH therapy beyond 6 months. This poses concern because, while the goal is to prevent recurrence of VTE, the risk of major bleeding with prolonged weight-adjusted LMWH therapy is significant. Potential solutions: There is a lack of data to inform on VTE treatment in cancer patients beyond the initial 3-6 months of anticoagulation. We propose that after a minimum of 3-6 months of therapeutic dose anticoagulation, the use of prophylactic doses of LMWH will have an acceptable and adherence profile in cancer patients with VTE. The data obtained from this study will help inform physician practices. Design: This is a multicentre, open-label study of enoxaparin (40 mg subcutaneous injection, once daily) for additional 6 months after an initial minimum 3-6-month course of therapeutic dose anticoagulant therapy. Patients: 150 patients with VTE secondary to cancer will take part in this multicentre study conducted in 8 Canadian centres within Quebec, Ontario and Nova Scotia. Study Outcomes: The primary objective of the study is to determine the rate of recurrent VTE in patients receiving prophylactic dose enoxaparin for secondary VTE prophylaxis after an initial minimum 3-6 months of anticoagulation. The secondary objective is to determine the safety profile of prophylaxis dose enoxaparin for secondary VTE prophylaxis after an initial 3-6 months of anticoagulation. This includes determining for all subjects: 1) cumulative incidence of major bleeding events; 2) cumulative incidence of clinically relevant non-major bleeding events; 3) cumulative incidence of minor bleeding event, and 4) overall survival during follow-up.

Conditions

Deep Vein Thrombosis

Outcome Measures

Primary Outcomes (1)

• Rate of recurrent VTE

  6 months

Secondary Outcomes (4)

• Cumulative incidence of major bleeding events

  6 months

• Cumulative incidence of clinically relevant non-major bleeding events

  6 months

• Cumulative incidence of minor bleeding events

  6 months

• Overall survival

  6 months

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Subjects will have an active malignancy defined as any of: a) diagnosis of cancer (excluding basal cell or squamous cell carcinoma) within 18 months of study enrolment; or b) have received treatment for cancer within 18 months (e.g. radiation therapy, chemotherapy, adjuvant therapy) of study enrolment; or c) have documented recurrent or metastatic cancer. Subjects must also have a first episode of objectively confirmed VTE (distal or proximal deep vein thrombosis (DVT) of the lower limb or proximal DVT of the upper limb, or pulmonary embolism (PE)) that is being treated with therapeutic anticoagulation for a minimum intended duration of 3-6 months. Subjects must be ≥18 years of age with a life expectancy of \> 6 months.

You may qualify if:

• Have an active malignancy defined as any of: a) Diagnosis of cancer (excluding basal cell or squamous cell carcinoma of the skin) within 18 months of enrollment; b) Have received treatment for cancer within 18 months (e.g. radiation therapy, chemotherapy, adjuvant therapy); c) Have documented recurrent or metastatic cancer
• Receiving a 3-6 month course of weight-adjusted LMWH for an acute, objectively confirmed, symptomatic VTE (proximal or distal DVT of the lower extremity, proximal DVT of the upper extremity, or PE)
• Age ≥ 18 years
• Life expectancy \> 6 months
• Able to comply with scheduled follow up visits
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
• Willing to provide written informed consent

You may not qualify if:

• Distal DVT of the upper extremity
• Recurrent VTE during the 3-6-month LMWH treatment period
• Major or clinically relevant non-major bleeding during the 3-6 month LMWH treatment period
• Risk of bleeding (e.g. recent neurosurgery, history of intracranial hemorrhage, acute gastroduodenal ulcer, etc.)
• Diagnosis of basal cell and squamous cell carcinoma of the skin or acute Leukemia
• Platelet count \< 50 x 109/L
• Creatinine clearance \<30ml/min (using the modified Cockcroft-Gault formula)
• On hemodialysis
• Known hypersensitivity to heparin, LMWHs, or pork products
• Known contraindication to the use of heparin (e.g. heparin-induced thrombocytopenia)
• Currently participating in another clinical trial involving anticoagulation therapy (with the exception of aspirin)
• Pregnancy or breastfeeding
• On an anticoagulant for a different indication
• Treating physician plans for weight-adjusted LMWH for longer than 3-6 months duration

Sponsors & Collaborators

• Dr. Vicky Tagalakis: lead
• Sanofi: collaborator

Study Sites (7)

Queen Elizabeth II Medical Centre

Halifax, Nova Scotia, B3H 1V7, Canada

Location

The Ottawa Hospital Research Institute

Ottawa, Ontario, K1H 8L6, Canada

Location

Hôpital Charles-Le Moyne

Greenfield Park, Quebec, J4V 2H1, Canada

Location

The Jewish General Hospital

Montreal, Quebec, H3T 1E2, Canada

Location

St-Mary's Hospital

Montreal, Quebec, H3T 1M5, Canada

Location

The McGill University Health Centre - Glen Site

Montreal, Quebec, H4A 3J1, Canada

Location

Hôpital Sacré-Coeur

Montreal, Quebec, H4J 1C5, Canada

Location

Related Publications (1)

• Popov J, Coelho S, Carrier M, Sperlich C, Solymoss S, Routhier N, Shivakumar S, Aibibula W, Kahn SR, Tagalakis V. Step down to 6 months of prophylactic-dose low molecular weight heparin after initial full-dose anticoagulation for the treatment of cancer-associated thrombosis (STEP-CAT): A pilot study. J Thromb Haemost. 2022 Aug;20(8):1868-1874. doi: 10.1111/jth.15760. Epub 2022 Jun 9.

  PMID: 35587536 DERIVED

MeSH Terms

Conditions

Venous Thrombosis

Condition Hierarchy (Ancestors)

Thrombosis; Embolism and Thrombosis; Vascular Diseases; Cardiovascular Diseases

Study Officials

• Vicky Tagalakis, MD, MSc

  The Lady Davis Insitute, Jewish General Hospital

  STUDY CHAIR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Attending Physician and Clinical Researcher

Study Record Dates

• First Submitted: April 25, 2016
• First Posted: April 27, 2016
• Study Start: May 1, 2016
• Primary Completion: November 9, 2018
• Study Completion: November 9, 2018
• Last Updated: November 26, 2018

Record last verified: 2018-11

Data Sharing

• IPD Sharing: Will not share

Locations

CA (7)