A Study to Learn About Real-world Utilization and Outcomes of Darolutamide and Other Androgen Receptor Pathway Inhibitors (ARPIs) for Newly Diagnosed Metastatic Hormone-sensitive Prostate Cancer (de Novo mHSPC) in US Urology Clinics

Purpose

Prostate cancer is the most common non-skin cancer among men in the United States. For some men, the cancer has already spread to other parts of the body at the time of diagnosis; this is called metastatic hormone-sensitive prostate cancer (mHSPC). Treatment for mHSPC has advanced significantly, with new standards of care involving androgen deprivation therapy (ADT) combined with drugs known as androgen receptor pathway inhibitors (ARPIs), sometimes alongside chemotherapy like docetaxel. Darolutamide is an ARPI that is approved by the FDA for treating mHSPC in a "triplet" combination with ADT and docetaxel. It is also used in a "doublet" combination with ADT alone. However, there is limited information on how darolutamide is used in real-world clinical settings for this condition, which creates a gap in knowledge for making treatment decisions. This study aims to fill that gap by analyzing real-world data from electronic medical records. The primary goal is to describe the characteristics of patients with newly diagnosed mHSPC who are treated with darolutamide (either as a doublet or triplet) in urology clinics across the US. The study will also examine drug use patterns and clinical outcomes for these patients. Additionally, the study will explore the characteristics of patients treated with other ARPIs (abiraterone acetate, enzalutamide, and apalutamide) and assess the feasibility of creating matched patient groups for future comparative research. Data will be collected retrospectively from a large network of community urology practices in the US.

Conditions

  • Prostatic Neoplasms
  • Metastatic Hormone-Sensitive Prostate Cancer

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male patients with evidence of de novo mHSPC during the study period - Initiation of ARPI therapy during the patient identification period and within ±90 days from the mHSPC diagnosis - Age ≥18 years at index date (ARPI initiation for mHSPC) - Initiation of ADT and/or docetaxel therapy within ±90 days from index date - At least 90 days of EMR activity prior to the index date - At least 90 days of EMR activity post-index, unless the patient died earlier.

Exclusion Criteria

  • History of other primary cancers (except non-melanoma skin cancer) - Use of PARP inhibitors, chemotherapy (other than docetaxel), immunotherapy or radiopharmaceuticals prior to index date - Evidence of castration resistance (CR) flag in the database any time before the index date or up to 90 days after the de novo mHSPC diagnosis - Clinical trial participation during the study period.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Arm Groups

ArmDescriptionAssigned Intervention
Darolutamide + ADT + docetaxel Patients receiving darolutamide in combination with androgen deprivation therapy with docetaxel
  • Drug: Darolutamide
    Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer
    Other names:
    • Nubeqa
Abiraterone acetate + ADT + docetaxel Patients receiving abiraterone acetate in combination with androgen deprivation therapy with docetaxel
  • Drug: Abiraterone acetate
    Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer
Enzalutamide + ADT Patients receiving enzalutamide in combination with androgen deprivation therapy
  • Drug: Enzalutamide
    Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer
Apalutamide + ADT Patients receiving apalutamide in combination with androgen deprivation therapy
  • Drug: Apalutamide
    Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer
Darolutamide + ADT Patients receiving darolutamide in combination with androgen deprivation therapy
  • Drug: Darolutamide
    Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer
    Other names:
    • Nubeqa
Abiraterone acetate + ADT Patients receiving abiraterone acetate in combination with androgen deprivation therapy
  • Drug: Abiraterone acetate
    Androgen receptor pathway inhibitor for treatment of metastatic hormone-sensitive prostate cancer

Recruiting Locations

Precision Point Specialty LLC PPS Analytics, a Specialty Networks LLC Company
Cleveland, Ohio 44114-2619

More Details

Status
Recruiting
Sponsor
Bayer

Study Contact

Bayer Clinical Trials Contact
(+)1-888-84 22937
clinical-trials-contact@bayer.com