Implementing a Tool to Identify Risk for Venous Thromboembolism in Cancer Patients
|ClinicalTrials.gov Identifier: NCT01602432|
Recruitment Status : Completed
First Posted : May 21, 2012
Last Update Posted : September 10, 2014
|Condition or disease|
|Venous Thromboembolism Deep-Vein Thrombosis Pulmonary Embolism Cancer|
Patients with Cancer have a risk for venous thromboembolism (VTE) including deep-vein thrombosis (DVT) and/or pulmonary embolism (PE) that is markedly higher than non-Cancer patients. An acute episode of VTE has deleterious effects on the quality of life and long-term survival of cancer patients. Cancer patients with VTE have survival rates that are only one third of otherwise identical patients without VTE. Once VTE is diagnosed over 10% of cancer patients suffer a further event while on standard therapy and over 5% suffer a major hemorrhagic event.
The best way to treat VTE is its prevention (thromboprophylaxis). Studies suggest that among ambulatory cancer patients, risk for VTE varies markedly between patients and that the lack of knowledge of this risk, delays diagnosis and hampers efforts to effectively prevent VTE. Therefore, the identification of patients at high-risk for VTE may enable faster diagnosis of VTE and better use of thromboprophylaxis.
Recent studies have developed a novel tool to stratify VTE risk in cancer patients before they initiate anti-cancer treatment. We hypothesized that this risk tool will accurately identify cancer patients at high-risk and that its implementation in our clinical practice will result in a faster clinical diagnosis of VTE.
Our objective is: a) to evaluate the ideal strategy to incorporate the tool in our clinical setting as seamlessly as possible, and b) to determine whether the tool accurately predicts risk and results in a faster investigation for VTE.
Patient eligibility will be determined during the patient's initial consult to the Ottawa Cancer Center after cancer diagnosis has been confirmed by the medical Oncologist and before initiation of anticancer treatment. Follow-up for this study will be for 12 months and patients will be seen at the time of scheduled appointments for cancer treatment.
|Study Type :||Observational|
|Actual Enrollment :||143 participants|
|Official Title:||Implementing a Tool to Identify Risk for Venous Thromboembolism in Cancer Patients|
|Study Start Date :||November 2012|
|Actual Primary Completion Date :||August 2013|
|Actual Study Completion Date :||August 2013|
High Risk Group
Defined as patients whose primary malignancy is located in the brain, bladder, lung, testicle, stomach, pancreas and lymphatic system and whose risk score before the beginning of anticancer treatment is ≥ 2 according to the Risk Stratification Method proposed by Khorana et al. (2008).
Based on this method, the model includes 5 predictive variables as follows:
Low high Risk Group
Defined as patients whose primary malignancy is located in the brain, bladder, lung, testicle, stomach, pancreas and lymphatic system and whose risk score before the beginning of anticancer treatment is < 2 according to the Risk Stratification Method proposed by Khorana et al. (2008).
In order to confirm the patient low risk status, we will draw a blood sample to determine serum levels of D- dimer and soluble P selectin in patients of this low risk group according to Ay et al. (2010). If levels of D-dimer are ≥ 1.44 µg/mL and/or soluble P selectin ≥ 53.1 ng/mL, we will add one point for each one of the increased biochemical marker and the total score recalculated.
- Risk for Venous Thromboembolism [ Time Frame: 1 year ]This outcome will be measured by the cummulative rates of VTE stratified by the different categories of risk as determined by the prediction tool during the time-frame of the study
- Timing to VTE detection [ Time Frame: 1 year ]This will be measured by the time elapsed between the first signs or symptoms associated with a symptomatic VTE as described by the patient and the time of confirming VTE diagnosis.
- Study Feasibility [ Time Frame: 1 year ]Feasibility will be assessed by: a) achieving an average enrollment rate of at least 39 cancer patients per month; and b) accomplishing a rate of withdrawals or loss to follow-ups equal or less than 10%
- Physicians acceptance [ Time Frame: 1 year ]This will be assessed by measurements of physician's satisfaction to the implementation of the Risk stratification tool at the end of the study period.
- Success of an IS/IT solution [ Time Frame: 1 year ]This outcome will be measured by the physician's satisfaction to the implementation of an automatic risk detection.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01602432
|Ottawa Hospital Cancer Center|
|Ottawa, Ontario, Canada, K1H 8L6|
|Principal Investigator:||Philip S Wells, MD||Ottawa Hospital Research Institute|