Real World Evidence Study on Metastatic Prostate Cancer in the Pirkanmaa Hospital District in Finland

NCT ID: NCT05701007

Last Updated: 2024-04-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-02-13

Study Completion Date

2024-04-10

Brief Summary

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Comprehensive understanding of the epidemiology and disease burden of metastatic prostate cancer patients in Finland is lacking. This study will address the following questions:

* What are the demographic and clinical characteristics of metastatic prostate cancer patients?
* How are metastatic prostate cancer patients currently treated and how effective are these treatments?
* How does the development of castration-resistance affect patient outcomes?
* What is the economic burden of metastatic prostate cancer?

Detailed Description

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Conditions

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Metastatic Castration Sensitive Prostate Cancer (mCSPC) Metastatic Castration Resistant Prostate Cancer (mCRPC)

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patients diagnosed with metastatic castration sensitive prostate cancer (mCSPC)

degarelix

Intervention Type DRUG

mCSPC

goserelin

Intervention Type DRUG

mCSPC

leuprorelin

Intervention Type DRUG

mCSPC

triptorelin

Intervention Type DRUG

mCSPC

Patients diagnosed with metastatic castration resistant prostate cancer (mCRPC)

abiraterone

Intervention Type DRUG

mCRPC

enzalutamide

Intervention Type DRUG

mCRPC

docetaxel

Intervention Type DRUG

mCRPC

apalutamide

Intervention Type DRUG

mCRPC

cabazitaxel

Intervention Type DRUG

mCRPC

Radium-223

Intervention Type DRUG

mCRPC

Lutetium-177

Intervention Type DRUG

mCRPC

Interventions

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abiraterone

mCRPC

Intervention Type DRUG

enzalutamide

mCRPC

Intervention Type DRUG

docetaxel

mCRPC

Intervention Type DRUG

apalutamide

mCRPC

Intervention Type DRUG

cabazitaxel

mCRPC

Intervention Type DRUG

Radium-223

mCRPC

Intervention Type DRUG

Lutetium-177

mCRPC

Intervention Type DRUG

degarelix

mCSPC

Intervention Type DRUG

goserelin

mCSPC

Intervention Type DRUG

leuprorelin

mCSPC

Intervention Type DRUG

triptorelin

mCSPC

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of prostate cancer between 1/1/2007 - 12/31/2022
* Resident of Pirkanmaa at index date (diagnosis of mCSPC and/or mCRPC)
* Detection of metastatic prostate cancer

Exclusion Criteria

* Prevalent mCSPC and mCRPC patients (mCSPC or mCRPC diagnosis date before 1/1/2014
* Patient has another cancer diagnosis or the patient has received chemotherapy other than docetaxel or cabazitaxel within 2 years of mPC diagnosis.
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer

Helsinki, , Finland

Site Status

Countries

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Finland

Related Links

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https://pmiform.com/clinical-trial-info-request?StudyID=C3441057

To obtain contact information for a study center near you, click here.

Other Identifiers

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PrCa-RWD

Identifier Type: OTHER

Identifier Source: secondary_id

C3441057

Identifier Type: -

Identifier Source: org_study_id

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