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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

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data 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