- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02963675
Incidence of Second Primary Malignancies in Prostate Cancer Patients With Bone Metastases - an Observational Retrospective Cohort Study in Sweden (SMARCOS)
Incidence of Second Primary MAlignancies in pRostate Cancer Patients With bOne Metastases - an Observational Retrospective Cohort Study in Sweden (SMARCOS)
Study Overview
Detailed Description
Prostate cancer (PC) is the most common non-cutaneous malignancy in men. Once it becomes metastatic, it poses a serious threat to the patients' quality of life and survival. The most common site of metastases is the skeletal system: Among castration-resistant prostate cancer patients bone metastases are involved in over 90% of metastatic cases.
The development of new treatments has led to improved quality of life and prolonged lifetime among castration-resistant prostate cancer patients with metastases (mCRPC). A recent randomized clinical trial indicated significant improvement in survival and quality of life among patients with bone metastases treated with alpha emitter radium-223 as compared with placebo. To further evaluate the safety profile of Radium-223 in patients with castration resistant prostate cancer with bone metastases, Radium-223 alpha Emitter Agent in non-intervention Safety Study in mCRPC popUlation for long-teRm Evaluation (the REASSURE study), an international prospective observational single-arm cohort study was implemented as a post-marking requirement requested by the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA).
In the case that new treatments improve the length and quality of life substantially, it can be challenging to obtain an appropriate comparison group in the post-authorization phase. This study is conducted to obtain information about prostate cancer patients with bone metastases before the end of 2013. The incidence of second primary malignancies and overall survival are of particular interest. Information from this study will serve as a historical reference for the REASSURE study
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Multiple Locations, Sweden
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Patients with PC diagnosis in 1.1.1998 - 31.12.2013 and with bone metastases diagnosis or bone-directed treatments in 1.1.1998 - 31.12.2013 will be initially included into the large study population. From this initial population, the main analyses will concentrate on the following two populations:
- Prostate cancer patients with bone metastases (mPC), and
- Castration-resistant prostate cancer patients with bone metastases (mCRPC)
Description
Inclusion Criteria:mPC population; if the following criteria are fulfilled:
A.) PC diagnosis in 1.1.1998 - 31.12.2011 B.) Bone metastases diagnosis in 1.1.1999 - 31.12.2011 mCRPC population; if the following criteria are fulfilled:
- PC diagnosis in 1.1.1998 - 31.12.2011
- Bone metastases diagnosis in 1.1.2007 - 31.12.2011
One of the following in 1.1.2006 - 31.12.2011 and before or at the same time with bone metastases diagnosis:
- Discontinuation of the initial chemical castration (androgen deprivation therapy, ADT), change of the agent or modality of ADT, or start of treatment for advanced PC after the primary ADT (including chemotherapy or mitoxantrone)
- Surgical castration and initiation of ADT treatment, chemotherapy or mitoxantrone afterwards
- Treatment with medication specific to either castration-resistant PC or mCRPC (cabazitaxel, enzalutamide or abiraterone).
- In a sensitivity analysis, also those who have had at least 6 months since the initiation of castration treatment before cohort entry date (bone metastases diagnosis) are included in the mCRPC population.
Exclusion Criteria:
- First PC diagnosis later than 2 months after the diagnosis of bone metastases, or
- Permanent residence not in Sweden or patient otherwise not contributing to the registers at least a year before the diagnosis of bone metastases (patient counted not contributing also if database existence less than a year before cohort entry), or
- Use of any radiopharmaceuticals for bone metastases (ATC code): Samarium (V10BX02), strontium (V10BX01), rhenium (V10BX03) or radium (V10XX03).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Group 1
Prostate cancer patients with bone metastases (mPC)
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Group 2
Castration-resistant prostate cancer patients with bone metastases (mCRPC)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Incidences of Second primary malignancies that are characterized by the following ICD-10 codes: C00-C76, C81-C96, D00-D09, D37-D48.
Time Frame: Up to 15 years
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Up to 15 years
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Incidences of any site-specific second primary malignancies
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Site-specific ICD-10 code groups from the range of all neoplasm codes C00 - D48
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Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Overall survival
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Pathologic fracture
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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ICD-10 codes: M49.5, M84.4,
M90.7
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Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Spinal cord compression
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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ICD-10 codes: M43.9, M48.5, G95.2, G95.8
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Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Surgery to bone
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Based on the Nordic Medico-Statistical Committee (NOMESCO) classification of surgical procedure codes (NCSP codes)
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Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Radiation to bone
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Based on NCSP codes
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Up to 15 years for mPC patients and up to 7 years for mCRPC patients
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 18105 (2010 NARSAD Young Investigator Award)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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