Incidence of Second Primary Malignancies in Prostate Cancer Patients With Bone Metastases - an Observational Retrospective Cohort Study in Sweden (SMARCOS)

February 8, 2018 updated by: Bayer

Incidence of Second Primary MAlignancies in pRostate Cancer Patients With bOne Metastases - an Observational Retrospective Cohort Study in Sweden (SMARCOS)

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 in patients with castration resistant prostate cancer are of particular interest. Information from this study will serve as a historical reference for the REASSURE study (Background incidence study)

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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 Information from this study will serve as a historical reference for the REASSURE study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

Observational

Enrollment (Actual)

15953

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Multiple Locations, Sweden

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Sampling Method

Non-Probability Sample

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:

  1. PC diagnosis in 1.1.1998 - 31.12.2011
  2. Bone metastases diagnosis in 1.1.2007 - 31.12.2011
  3. One of the following in 1.1.2006 - 31.12.2011 and before or at the same time with bone metastases diagnosis:

    1. 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)
    2. Surgical castration and initiation of ADT treatment, chemotherapy or mitoxantrone afterwards
    3. Treatment with medication specific to either castration-resistant PC or mCRPC (cabazitaxel, enzalutamide or abiraterone).
    4. 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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Group 1
Prostate cancer patients with bone metastases (mPC)
Group 2
Castration-resistant prostate cancer patients with bone metastases (mCRPC)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
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
Up to 15 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
Site-specific ICD-10 code groups from the range of all neoplasm codes C00 - D48
Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Overall survival
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Pathologic fracture
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
ICD-10 codes: M49.5, M84.4, M90.7
Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Spinal cord compression
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
ICD-10 codes: M43.9, M48.5, G95.2, G95.8
Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Surgery to bone
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Based on the Nordic Medico-Statistical Committee (NOMESCO) classification of surgical procedure codes (NCSP codes)
Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Radiation to bone
Time Frame: Up to 15 years for mPC patients and up to 7 years for mCRPC patients
Based on NCSP codes
Up to 15 years for mPC patients and up to 7 years for mCRPC patients

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 15, 2016

Primary Completion (Actual)

March 31, 2017

Study Completion (Actual)

March 31, 2017

Study Registration Dates

First Submitted

November 10, 2016

First Submitted That Met QC Criteria

November 10, 2016

First Posted (Estimate)

November 15, 2016

Study Record Updates

Last Update Posted (Actual)

February 12, 2018

Last Update Submitted That Met QC Criteria

February 8, 2018

Last Verified

February 1, 2018

More Information

Terms related to this study

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.

Clinical Trials on Prostatic Neoplasms

3
Subscribe