An Observational Study Called H2H-OSCAR-US to Learn More About How Well Rivaroxaban Works and How Safe it is Compared to Apixaban Under Real World Conditions in People in the US With Cancer Who Have Problems Due to Formation of Blood Clots in the Veins (Venous Thromboembolism)

NCT05461807 | Completed

• 1 other identifier: 22290
• Study Type: observational
• Target: 2,437
• Locations: 1 country
• Sites: 1

Brief Summary

This is an observational study in which patient data from the past on venous thromboembolism (VTE) in people with cancer is studied. In observational studies, only observations are made without specified advice or interventions. People with VTE have problems due to the formation of blood clots in the veins. Blood clots can reduce the flow of blood to vital organs such as the lungs, which can lead to their damage. VTE can also be "recurrent". This means that the blood clots have returned after treatment. People who have cancer are more likely to develop VTE, recurrent clots, and bleeding on blood thinning treatments. To prevent the formation of new or recurrent clots in people with cancer, a newer type of blood thinner is available, called direct-acting oral anticoagulant (DOAC). Rivaroxaban and apixaban are the most used DOACs in the US. They work by blocking a certain step in the blood clotting process, the activation of a protein called Factor X. Previous studies show that DOACs may reduce clot risk compared to other available treatments but may potentially lead to more frequent bleeding. Studies looking at these points in direct comparison of rivaroxaban and apixaban a currently missing. Therefore, this study will collect real-world data from the US to learn how well rivaroxaban works and how safe it is compared to apixaban in people with cancer and VTE who are at low risk for bleeding. To do this, researchers will look at the proportion of patients that will develop:

• recurrent blood clots in the veins after treatment
• bleeding in a critical organ
• bleeding that requires a hospital stay within 3 and 6 months after participants had a VTE that was treated with rivaroxaban or apixaban. De-identified data collected will cover 12 months before and at maximum 6 months after this VTE. They will come from US electronic health records and will cover the years 2012 to 2020. No visits or tests are required as part of this study.

Conditions

Treatment of Venous Thromboembolism in Cancer Patients; Venous Thromboembolism; Cancer

Outcome Measures

Primary Outcomes (5)

• Composite of recurrent VTE (fatal and non-fatal) or any bleed resulting in hospitalization (per the Cunningham algorithm) at 3 months

  Retrospective data analysis from January,2013 to December,2020

• Composite of recurrent VTE (fatal and non-fatal) or any critical organ bleed (intracranial, intraspinal, intraocular, retroperitoneal, intraarticular, or pericardial, or intramuscular with compartment syndrome) at 3 months

  Retrospective data analysis from January,2013 to December,2020

• Recurrent VTE (fatal and non-fatal) at 3 months

  Retrospective data analysis from January,2013 to December,2020

• Any bleed resulting in hospitalization (per the Cunningham algorithm) at 3 months

  Retrospective data analysis from January,2013 to December,2020

• Critical organ bleeding (intracranial, intraspinal, intraocular, retroperitoneal, intraarticular, or pericardial, or intramuscular with compartment syndrome) at 3 months

  Retrospective data analysis from January,2013 to December,2020

Secondary Outcomes (5)

• Composite of recurrent VTE (fatal and non-fatal) or any bleed resulting in hospitalization (per the Cunningham algorithm) at 6 months

  Retrospective data analysis from January,2013 to December,2020

• Composite of recurrent VTE (fatal and non-fatal) or any critical organ bleed (intracranial, intraspinal, intraocular, retroperitoneal, intraarticular, or pericardial, or intramuscular with compartment syndrome) at 6 months

  Retrospective data analysis from January,2013 to December,2020

• Recurrent VTE (fatal and non-fatal) at 6 months

  Retrospective data analysis from January,2013 to December,2020

• Any bleed resulting in hospitalization (per the Cunningham algorithm) at 6 months

  Retrospective data analysis from January,2013 to December,2020

• Critical organ bleeding (intracranial, intraspinal, intraocular, retroperitoneal, intraarticular, or pericardial, or intramuscular with compartment syndrome) at 6 months

  Retrospective data analysis from January,2013 to December,2020

Study Arms (1)

Cancer patients with venous thromboembolism (VTE)

Adults diagnosed with active (primary or metastatic) cancer excluding oesophageal, gastric, unresected colorectal, bladder, central nervous system cancers (except brain) and leukaemia (a cohort of CAT (Cancer-associated thrombosis) patients at a low risk for bleeding, which is defined as per the ISTH (International Society on Thrombosis and Haemostasis) guidelines), admitted to the hospital, emergency department or observation unit for acute DVT (Deep vein thrombosis) and/or PE (Pulmonary embolism) on or after January 1, 2013 (to correspond with the US availability of rivaroxaban for VTE treatment), being treated with a therapeutic VTE dose of rivaroxaban or apixaban on day 7 post-acute VTE diagnosis (index date).

Drug: Rivaroxaban (Xarelto, BAY59-7939); Drug: Apixaban

Interventions

Rivaroxaban (Xarelto, BAY59-7939) DRUG

Retrospective cohort analysis using United States Optum De-Identified Electronic Health Records data

Cancer patients with venous thromboembolism (VTE)

Apixaban DRUG

Retrospective cohort analysis using United States Optum De-Identified Electronic Health Records data

Cancer patients with venous thromboembolism (VTE)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Adults diagnosed with active (primary or metastatic) cancer excluding oesophageal, gastric, unresected colorectal, bladder, central nervous system cancers (except brain) and leukaemia (a cohort of CAT patients at a low risk for bleeding, which is defined as per ISTH guidelines), experiencing a hospital, emergency department, or observation unit admission with a primary diagnosis code for VTE, who received therapeutic VTE doses of rivaroxaban or apixaban as their first outpatient anticoagulant (index event) within 7-days of the acute VTE event and were active in the data set for at least 12-months prior to the CAT event and with at least one provider visit in the 12-months prior to the acute CAT event (establishing a 12-month look back/baseline period).

You may qualify if:

• Be ≥18 years of age at the time of anticoagulation initiation.
• Have active cancer defined as cancer being actively treated, diagnosed within 6-months prior of the index CAT or associated with metastatic disease (regardless of time from initial cancer diagnosis)
• Admitted to the hospital, emergency department or observation unit for acute Deep vein thrombosis (DVT) and/or Pulmonary embolism (PE)
• Started on a therapeutic VTE dose of rivaroxaban or apixaban within 7 days of the qualifying VTE event and treated with a therapeutic VTE dose of rivaroxaban or apixaban as their first anticoagulant on day 7 post-acute CAT event diagnosis (index date) to increase the probability of accurately classifying patients' intended outpatient anticoagulant for CAT treatment, and that, patients are compared at the same point from diagnosis.
• Have been active in the data set for at least 12-months prior to the index event (based on the "First Month Active" field) and had at least one provider visit in the 12-months prior to the acute VTE event (baseline period).

You may not qualify if:

• Oesophageal, gastric, unresected colorectal, bladder, central nervous system cancers (except brain) and leukaemia
• Evidence of atrial fibrillation, recent hip/knee replacement (within 35 days of index VTE), ongoing VTE treatment, valvular heart disease defined as any rheumatic heart disease, mitral stenosis, or mitral valve repair/replacement.
• Pregnancy.
• Initiation of non-therapeutic VTE doses of rivaroxaban or apixaban.
• Evidence of anticoagulation use written prescription or patient self-report during the 12-months prior to the qualifying CAT event per.

Sponsors & Collaborators

• Bayer: lead
• Janssen Research & Development, LLC: collaborator

Study Sites (1)

Bayer

Wuppertal, 42096, Germany

Location

Related Publications (1)

• Caroti KS, Becattini C, Carrier M, Cohen AT, Ekbom A, Khorana AA, Lee AYY, Brescia C, Abdelgawwad K, Psaroudakis G, Rivera M, Schaefer B, Brobert G, Coleman CI. Rivaroxaban versus Apixaban for Treatment of Cancer-Associated Venous Thromboembolism in Patients at Lower Risk of Bleeding. TH Open. 2023 Jul 10;7(3):e206-e216. doi: 10.1055/s-0043-1770783. eCollection 2023 Jul.

  PMID: 37435565 DERIVED

Related Links

• Click here to find information for studies related to Bayer products. To find this study enter the ClinicalTrials.gov identifier (NCT) number or Bayer Study Identifier (ID) in the search field.

MeSH Terms

Conditions

Venous Thromboembolism; Neoplasms

Interventions

Rivaroxaban; apixaban

Condition Hierarchy (Ancestors)

Thromboembolism; Embolism and Thrombosis; Vascular Diseases; Cardiovascular Diseases

Intervention Hierarchy (Ancestors)

Thiophenes; Sulfur Compounds; Organic Chemicals; Morpholines; Oxazines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 14, 2022
• First Posted: July 18, 2022
• Study Start: July 14, 2022
• Primary Completion: October 5, 2022
• Study Completion: October 5, 2022
• Last Updated: October 26, 2022

Record last verified: 2022-10

Data Sharing

• IPD Sharing: Will not share

Locations

DE (1)