Screening for Occult Malignancy Using 18F-Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography (FDG PET/CT) in Patients with Unprovoked Venous Thromboembolism

Who is this study for? Older adult patients with Venous Thromboembolism from an active Malignancy
Status: Recruiting
Location: See all (20) locations...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Venous thromboembolism (VTE) can be the earliest sign of cancer. Identifying occult cancers at the time of VTE diagnosis may lead to significant improvement of patients' care. This is also an upmost issue for patients who want to know if an underlying cancer might have triggered the VTE. An individual patient-level data meta-analysis (IPDMA) supports extensive screening strategies for occult cancer especially based on FDG PET/CT, and suggests that the best target population for cancer screening would be patients with unprovoked VTE older than 50 years of age (6.7% in patients aged 50 years or more vs. 1.0% in patients of less than 50 years (OR: 7.1, 95% CI: 3.1 to 16%).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
View:

⁃ Patients aged 50 years or older with a new diagnosis of first unprovoked proximal deep vein thrombosis (DVT) and/or pulmonary embolism (PE) will be eligible to participate into the study.

⁃ Unprovoked VTE is defined as the absence of any of the following predisposing factors:

• active malignancy (known malignancy, progressive and/or treated during the last 5 years) except for adequately treated basal or squamous cell carcinoma; Patients whose state of health suggests the presence of cancer at the time of diagnosis of VTE cannot be included in the protocol

• recent (less than 3 months) paralysis, paresis or plaster immobilization of the lower extremities;

• recently bedridden for period of 3 or more days, or major surgery, within the previous 12 weeks requiring general or regional anaesthesia;

• previous unprovoked VTE;

• known thrombophilia (hereditary or acquired)

Locations
Other Locations
Canada
University of Calgary
NOT_YET_RECRUITING
Calgary
McMaster University
NOT_YET_RECRUITING
Hamilton
London Health Sciences Centre
NOT_YET_RECRUITING
London
Jewish General Hospital
RECRUITING
Montreal
McGill University Health Centre
NOT_YET_RECRUITING
Montreal
Hopital Montfort
RECRUITING
Ottawa
Ottawa Hospital Research Institute
RECRUITING
Ottawa
Sunnybrook Research Institute
RECRUITING
Toronto
University Health Network
RECRUITING
Toronto
University of Manitoba
NOT_YET_RECRUITING
Winnipeg
France
CH Agen
RECRUITING
Agen
CHU Angers
RECRUITING
Angers
Brest University Hospital
RECRUITING
Brest
CHU de Clermont-Ferrand
RECRUITING
Clermont-ferrand
CHU de Dijon
RECRUITING
Dijon
CHU de Limoges
RECRUITING
Limoges
CH des Pays de Morlaix
RECRUITING
Morlaix
Hôpital Européen Georges Pompidou
RECRUITING
Paris
CHU Saint-Etienne
RECRUITING
Saint-etienne
Hôpital Saint Musse - CH Toulon
RECRUITING
Toulon
Contact Information
Primary
Pierre-Yves SALAUN
pierre-yves.salaun@chu-brest.fr
(+33)298223327
Backup
Aurélien DELLUC
adelluc@toh.ca
Time Frame
Start Date: 2020-09-08
Estimated Completion Date: 2030-09-08
Participants
Target number of participants: 1276
Treatments
Active_comparator: Limited cancer screening
Limited screening alone.
Experimental: Limited cancer screening + FDG PET/CT
Limited screening + FDG PET/CT
Authors
Grégoire LE GAL, Francis COUTURAUD
Sponsors
Collaborators: Canadian Institutes of Health Research (CIHR), Ministry of Health, France, Ottawa Hospital Research Institute
Leads: University Hospital, Brest

This content was sourced from clinicaltrials.gov