Skip to content

Study to Gather Information About the Use of Healthcare Services and the Way the Disease is Cared for in Canadian Patients With Prostate Gland Cancer Which Spread Throughout the Body

Real World Evaluation of Access-driven Canadian Treatment Sequences in Progressive Prostate Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04281147
Acronym
REACTIVATE
Enrollment
4301
Registered
2020-02-24
Start date
2020-02-24
Completion date
2021-06-22
Last updated
2022-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

Metastatic castrate resistant prostate cancer mCRPC

Brief summary

Study to gather information about the optimal placement of Ra-223 in the order of different treatments in terms of the effect on patients and in terms of the use of healthcare services for the treatment of Canadian patients with prostate gland cancer which spread to other parts of the body. In order to collect this information real world data from prostate gland cancer patients from four Canadian administrative databases will be analyzed. Data collected from patients treated with their 2nd line of life-prolonging therapy for Non-Metastatic Castration Resistant Prostate Cancer (mCRPC) initiated from 01 Jan 2012 to 31 Dec 2017. For patients included in the study, all available data from the beginning for their record until death, lost to follow-up or database cut-off will be included. The index date is the date of initiation of the 2nd line life-prolonging therapy for mCRPC.

Interventions

DRUGRadium-223 dichloride (Xofigo, BAY88-8223)

Follow clinical administration

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* Use of at least 2 lines of life-prolonging mCRPC therapy * The 2nd line of life-prolonging therapy was initiated between 01-Jan-2012 to 31-Dec-2017

Exclusion criteria

\- No formal

Design outcomes

Primary

MeasureTime frameDescription
Overall survivalRetrospective analysis from 01-Jan-2012 to 31-Dec-2017The length of time from the date of initiation of 2nd line life-prolonging therapy to death due to any cause

Secondary

MeasureTime frameDescription
Average length of hospital stays (number of days)Retrospective analysis from 01-Jan-2012 to 31-Dec-2017Measured from the initiation of 2nd line life -prolonging therapy (index date) until death
Time to first Emergency Room (ER) visitRetrospective analysis from 01-Jan-2012 to 31-Dec-2017Measured from the start of 2nd line life-prolonging therapy (index date) until the first ER visit.
Event-free survival (EFS)Retrospective analysis from 01-Jan-2012 to 31-Dec-2017The length of time from the start of 2nd line life-prolonging therapy to the earliest occurrence of one of the following: * A change in life-prolonging treatment * Death from any cause
Number of overnight hospital staysRetrospective analysis from 01-Jan-2012 to 31-Dec-2017Measured from the initiation of 2nd line life-prolonging therapy (index date) until death
Total incidence of EBRTRetrospective analysis from 01-Jan-2012 to 31-Dec-2017Total number of EBRT treatments received over the course of the patient's journey starting from the initiation of 2nd line life-prolonging therapy (index date) until death.
Time to first hospitalizationRetrospective analysis from 01-Jan-2012 to 31-Dec-2017Measured from the start of the 2nd line life-prolonging therapy (index date) until the first overnight hospital stay.
Number of visits to the ERRetrospective analysis from 01-Jan-2012 to 31-Dec-2017Measured from the initiation of 2nd line life-prolonging therapy (index date) until death
Time to External Beam Radiation Therapy (EBRT)Retrospective analysis from 01-Jan-2012 to 31-Dec-2017From the start of the 1st life-prolonging therapy (index date) until the first use of EBRT

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026