Using a Blood Test and Software Tool to Guide Treatment for Venous Thromboembolism
Key facts
- Who runs it
- Memorial Sloan Kettering Cancer Center
- Where
- Basking Ridge, Commack, Harrison, Middletown, Montvale, New York, and Rockville Centre, United StatesSee the 7 sitesAlso in 1 other country, 1 site
- Trial code
- Status
- Recruiting
- People taking part
- 259 people, planned
- Started
- 30 Jan 2026
- Expected to end
- 30 Jan 2030
- Type of study
- Interventional, 2 groups
- Treatments tested
- MSK-ACCESS
- ctDNA/VTE Risk Score:
- Record updated
- 9 November 2026
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 11 criteriaShow less
Who can take part
- Age ≥ 18 with a history of cancer-associated VTE (objectively confirmed symptomatic or incidental/unsuspected proximal lower-limb DVT, symptomatic pulmonary embolism [PE] or incidental PE in a segmental or more proximal pulmonary artery) and completion of between 3 and 12 months of anticoagulation with enoxaparin, dalteparin,rivaroxaban, or apixaban without current VTE-related symptoms (imaging to confirm resolution not required); Diagnosis of DVT requires evidence of one or more filling defects at compression ultrasonography, venography, CT venography, or MR venography involving at least the popliteal or more proximal veins; Diagnosis of PE requires an intraluminal filling defect in segmental or more proximal arteries
- Diagnosis of one of the following solid tumors in either advanced (i.e. unresectable) stage or receiving systemic anticancer treatment within six weeks of enrollment (maintenance therapy included):; breast cancer regardless of cytotoxic-chemotherapy status; hepatobiliary cancer regardless of cytotoxic-chemotherapy status; prostate cancer regardless of cytotoxic-chemotherapy status; non-small cell lung cancer with cytotoxic-chemotherapy received within 30 days; pancreatic cancer with cytotoxic-chemotherapy received within 30 days; bladder cancer with cytotoxic-chemotherapy received within 30 days
- Signed and dated informed consent by study participant/Legally Authorized Representative (LAR)
Who cannot take part
- Contraindication to discontinuation of anticoagulation (examples include but not limited to: known antiphospholipid syndrome or factor V leiden, active arterial thrombus, catheter-associated thrombus, on anticoagulation for atrial fibrillation or other non-oncologic reasons)
- Diagnosis of an active hematologic malignancy
- History of major bleeding in the last six months (major bleeding defined as fatal bleeding, and/or symptomatic bleeding in a critical area or organ, such as intracranial, intraspinal, intraocular, retroperitoneal, intra-articular or pericardial, or intramuscular with compartment syndrome; bleeding that necessitates acute surgical intervention; bleeding causing a fall in hemoglobin levels of 1.24 mmol/L (2 g/dL or greater) or more; or bleeding leading to a transfusion of 2 U or more of whole blood or red cells)
- Contraindication to ongoing anticoagulation
- Known diagnosis of disseminated intravascular coagulation (DIC)
- Suspicion for tumor thrombus on the imaging leading to original diagnosis of VTE
- Enrolled in hospice care
- Currently has inferior vena cava (IVC) filter
Where in United States
Also in 1 other country, 1 site
- Memorial Sloan Kettering Cancer Center Basking Ridge (All Protocol Activities)Basking Ridge, United StatesContact: Justin Jee, MD, PhDTaking people
- Memorial Sloan Kettering Suffolk - Commack (Limited Protocol Activities)Commack, United StatesContact: Justin Jee, MD, PhDTaking people
- Memorial Sloan Kettering Westchester (All Protocol Activities)Harrison, United StatesContact: Justin Jee, MD, PhDTaking people
- Memorial Sloan Kettering Monmouth (All Protocol Activities)Middletown, United StatesContact: Justin Jee, MD, PhDTaking people
- Memorial Sloan Kettering Bergen (All Protocol Activities)Montvale, United StatesContact: Justin Jee, MD, PhDTaking people
- Memorial Sloan Kettering Cancer Center (All Protocol Activites)New York, United StatesContact: Justin Jee, MD, PhDTaking people
- Memorial Sloan Kettering Nassau (All Protocol Activities)Rockville Centre, United StatesContact: Justin Jee, MD, PhDTaking people
About the trial
What the trial wants to find out
The purpose of this study is to find out whether a software tool, ctDNA/VTE (Venous Thromboembolism) risk score model, is an effective way to predict the likelihood of VTE coming back in people who have received anticoagulant treatment.
The 2 groups in the trial
- High risk for recurrent Venous Thromboembolism/VTETreatment being tested
Participants with a ≤5% chance of Venous Thromboembolism/VTE according to the model will be designated "low risk" for the purposes of the study; all other participants will be considered "high risk.
Treatment: MSK-ACCESS and ctDNA/VTE Risk Score:
- Low-risk for recurrent Venous Thromboembolism/VTETreatment being tested
Participants with a ≤5% chance of Venous Thromboembolism/VTE according to the model will be designated "low risk" for the purposes of the study; all other participants will be considered "high risk.
Treatment: MSK-ACCESS and ctDNA/VTE Risk Score:
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- A Nonrandomized Trial Using DNA Liquid Biopsies to Guide Anticoagulation For Patients With Cancer-Associated Thromboembolism
- Record updated
- 9 November 2026