Apixaban or Dalteparin in Reducing Blood Clots in Patients With Cancer Related Venous Thromboembolism

Phase 3

Completed

• Conditions: Cerebral Vein Thrombosis; Malignant Neoplasm; Portal Vein Thrombosis; Renal Vein Thrombosis; Splenic Thrombosis; Venous Thromboembolism; Gonadal Thrombosis; Mesenteric Thrombosis; Metastatic Malignant Neoplasm; Pulmonary Embolism
• Interventions: Drug: Apixaban; Drug: Dalteparin; Other: Questionnaire Administration

• Registration Number: NCT02585713
• Lead Sponsor: Academic and Community Cancer Research United

Brief Summary

This randomized phase III trial studies the side effects of and compares apixaban and dalteparin in reducing blood clots in patients with cancer-related venous thromboembolism. Venous thromboembolism is a condition in which a blood clot forms in a vein and then breaks off and moves through the bloodstream. Patients with cancer are at increased risk for venous thromboembolism. Apixaban and dalteparin are drugs used to prevent blood clots from forming or to treat blood clots that have formed. It is not yet known whether apixaban or dalteparin is more effective in reducing blood clots in patients with cancer related venous thromboembolism.

ADAM-VTE

Detailed Description

PRIMARY OBJECTIVES:

I. Any episode of major bleeding including fatal bleeding.

SECONDARY OBJECTIVES:

I. Venous thromboembolism (VTE) recurrence including deep vein thrombosis (DVT), pulmonary embolism (PE), fatal PE, or arterial thromboembolism.

II. Any episode of major bleeding including fatal bleeding or any episode of clinically relevant non-major bleeding.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive apixaban 10 mg orally (PO) twice daily (BID) on days 1-7 and lower-dose apixaban 5 mg PO BID on days 8-180.

ARM II: Patients receive dalteparin 200 international units (IU)/kg/day subcutaneously (SC) once daily (QD) on days 1-30 and lower-dose dalteparin 150 IU/kg/day SC QD on days 31-180.

After completion of study treatment, patients are followed up at 3 months.

Study Timeline

• Study First Submitted: 2015-10-22
• Study First Submitted QC: 2015-10-22
• Study First Posted: 2015-10-23
• Study Start: 2015-11-20
• Primary Completion: 2018-04-02
• Status Verified: 2019-06
• Results First Submitted: 2019-10-21
• Results First Submitted QC: 2019-12-09
• Study Completion: 2019-12-24
• Results First Posted: 2019-12-24
• Last Update Submitted: 2020-07-31
• Last Update Posted: 2020-08-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• Confirmed acute lower extremity or upper extremity (jugular, innominate, subclavian, axillary, brachial) DVT, PE, splanchnic (hepatic, portal, splenic, mesenteric, renal, gonadal), or cerebral vein thrombosis
• Active cancer defined as metastatic disease and/or any evidence of cancer on cross-sectional or positron emission tomography (PET) imaging, cancer related surgery, chemotherapy or radiation therapy within the past 6 months; note: non-melanoma skin cancer does not meet the cancer requirement
• Life expectancy >= 60 days
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1, or 2
• Obtained =< 30 days prior to randomization: Platelet count >= 50,000/mm^3
• Obtained =< 30 days prior to randomization: Alanine aminotransferase (ALT) or aspartate transaminase (AST) =< 3 x upper limit of normal (ULN)
• Obtained =< 30 days prior to randomization: International normalized ratio (INR) =< 1.6 (if not taking anticoagulant therapy)
• Obtained =< 30 days prior to randomization: Calculated creatinine clearance must be >= 30 ml/min using the Cockcroft-Gault formula
• Negative serum or urine pregnancy test done =< 24 hours prior to randomization, for women of childbearing potential only; note: a women of childbearing potential (WOCBP) is defined as any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy or bilateral oophorectomy) and is not postmenopausal; menopause is defined as 12 months of amenorrhea in a woman over age 45 years in the absence of other biological or physiological causes
• Ability to complete questionnaire(s) by themselves or with assistance
• Ability to provide informed written consent
• Willing to return to enrolling institution for follow-up (during the Active Monitoring Phase of the study)

Exclusion Criteria

• Any of the following:

  • Pregnant women

  • Nursing women

  • Men or women of childbearing potential who are unwilling to employ adequate contraception

    • Note: women of child bearing potential must agree to follow instructions for method(s) of contraception for the duration of treatment with study drug (s) plus 33 days after finishing the last dose
    • Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with study drug (s) plus 93 days after finishing the last dose
    • Azoospermic males and WOCBP who are continuously not heterosexually active are exempt from contraceptive requirements; however they must still undergo pregnancy testing as described in this section

• Note: investigators shall counsel WOCBP and male subjects who are sexually active with WOCBP on the importance of pregnancy prevention and the implications of an unexpected pregnancy Investigators shall advise WOCBP and male subjects who are sexually active with WOCBP on the use of highly effective methods of contraception; highly effective methods of contraception have a failure rate of < 1% when used consistently and correctly

• At a minimum, subjects must agree to the use of one method of highly effective contraception as listed below:

  • HIGHLY EFFECTIVE METHODS OF CONTRACEPTION

    • Male condoms with spermicide

    • Hormonal methods of contraception including combined oral contraceptive pills, vaginal ring, injectables, implants and intrauterine devices (IUDs) such as Mirena by WOCBP subject or male subject?s WOCBP partner

    • Female partners of male subjects participating in the study may use hormone based contraceptives as one of the acceptable methods of contraception since they will not be receiving study drug

    • IUDs, such as ParaGard

    • Tubal ligation

    • Vasectomy

    • Complete abstinence

      • Complete abstinence is defined as complete avoidance of heterosexual intercourse and is an acceptable form of contraception for all study drugs; female subjects must continue to have pregnancy tests; acceptable alternate methods of highly effective contraception must be discussed in the event that the subject chooses to forego complete abstinence

• Treatment with an anticoagulant for more than 7 days for the current blood clot, prior to randomization

• Active bleeding

• Severe hypersensitivity reaction to apixaban, dalteparin, heparin or pork products (e.g., anaphylactic reactions)

• Use of the following CYP3A4 inducers: rifampin, rifabutin, carbamazepine, efavirenz, phenobarbital, phenytoin, fosphenytoin, primidone, and St. John?s wort)

• Thienopyridine therapy (clopidogrel, prasugrel, or ticagrelor) that will be continued on study

• Severe liver disease (known cirrhosis Childs Pugh class B or C), or active hepatitis

• Use of a Factor Xa inhibitor (e.g. apixaban, rivaroxaban, or edoxaban) =< 3 months prior to randomization

• Treatment of a thromboembolic event =< 6 months prior to randomization

• Documented venous thromboembolism while on therapeutic anticoagulation (?anticoagulation failure?)

• Mechanical heart valve

• Documented hemorrhagic tendencies

• Bacterial endocarditis

• History of heparin induced thrombocytopenia

• Any of the following conditions:

  • Intracranial bleeding =< 6 months prior to randomization
  • Intraocular bleeding =< 6 months prior to randomization
  • Gastrointestinal bleeding and/or endoscopically proven ulcer =< 6 months prior to randomization
  • Head trauma or major trauma =<1 month prior to randomization
  • Neurosurgery =< 2 weeks prior to randomization
  • Major surgery =< 1 week prior to randomization
  • Overt major bleeding at the time of randomization
  • Gross hematuria at the time of randomization

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Arm I (apixaban)	Apixaban	Patients receive apixaban 10 mg PO BID on days 1-7 and lower-dose apixaban 5 mg PO BID on days 8-180.
Arm I (apixaban)	Questionnaire Administration	Patients receive apixaban 10 mg PO BID on days 1-7 and lower-dose apixaban 5 mg PO BID on days 8-180.
Arm II (dalteparin)	Questionnaire Administration	Patients receive dalteparin 200 IU/kg/day SC QD on days 1-30 and lower-dose dalteparin 150 IU/kg/day SC QD on days 31-180.
Arm II (dalteparin)	Dalteparin	Patients receive dalteparin 200 IU/kg/day SC QD on days 1-30 and lower-dose dalteparin 150 IU/kg/day SC QD on days 31-180.

Primary Outcome Measures

Name	Time	Method
6 Month Bleeding Rate	Up to 6 months	The rate (percentage) of patients experiencing major bleeding at 6 months from treatment initiation and its associated 95% confidence interval was estimated separately by treatment arm using a cumulative incidence function, treating death without bleeding as a competing risk.

Secondary Outcome Measures

Name	Time	Method
Composite Bleeding Rate: Major Bleed or a Clinically Relevant Non-major Bleed	Up to 6 months	A similar analysis as described for the primary safety analysis will be used. The rate (percentage) of patients experiencing major bleeding or a clinically relevant non-major bleed at 6 months from treatment initiation and its associated 95% confidence interval was estimated separately by treatment arm using a cumulative incidence function, treating death without bleeding as a competing risk.
Time to the First Event of the Composite Deep Vein Thrombosis (DVT)/Pulmonary Embolism (PE)	Up to 3 months post-treatment	Analyzed using the same methods described above for the primary endpoint.Time to the first event of the composite deep vein thrombosis (DVT)/pulmonary embolism (PE) is defined as the time from randomization to the date the patient experienced the first event of the composite deep vein thrombosis (DVT)/pulmonary embolism (PE).

Trial Locations

Locations (18)

Mayo Clinic in Arizona; 🇺🇸 Scottsdale, Arizona, United States

Cancer Research Consortium of West Michigan NCORP; 🇺🇸 Grand Rapids, Michigan, United States

Mayo Clinic in Florida; 🇺🇸 Jacksonville, Florida, United States

Illinois CancerCare-Peoria; 🇺🇸 Peoria, Illinois, United States

University of Iowa/Holden Comprehensive Cancer Center; 🇺🇸 Iowa City, Iowa, United States

Cancer Center of Kansas - Wichita; 🇺🇸 Wichita, Kansas, United States

Rapid City Regional Hospital; 🇺🇸 Rapid City, South Dakota, United States

Toledo Clinic Cancer Centers-Toledo; 🇺🇸 Toledo, Ohio, United States

New Hampshire Oncology Hematology PA-Hooksett; 🇺🇸 Hooksett, New Hampshire, United States

Metro Minnesota Community Oncology Research Consortium; 🇺🇸 Saint Louis Park, Minnesota, United States

NorthShore University HealthSystem-Evanston Hospital; 🇺🇸 Evanston, Illinois, United States

Siouxland Regional Cancer Center; 🇺🇸 Sioux City, Iowa, United States

Mayo Clinic; 🇺🇸 Rochester, Minnesota, United States

University of Nebraska Medical Center; 🇺🇸 Omaha, Nebraska, United States

Guthrie Medical Group PC-Robert Packer Hospital; 🇺🇸 Sayre, Pennsylvania, United States

Coborn Cancer Center at Saint Cloud Hospital; 🇺🇸 Saint Cloud, Minnesota, United States

FirstHealth of the Carolinas-Moore Regional Hosiptal; 🇺🇸 Pinehurst, North Carolina, United States

Columbus NCI Community Oncology Research Program; 🇺🇸 Columbus, Ohio, United States