TY - JOUR
T1 - Research Protocol for an Observational Health Data Analysis on the Adverse Events of Systemic Treatment in Patients with Metastatic Hormone-sensitive Prostate Cancer
T2 - Big Data Analytics Using the PIONEER Platform
AU - Rajwa, Pawel
AU - Borkowetz, Angelika
AU - Abbott, Thomas
AU - Alberti, Andrea
AU - Bjartell, Anders
AU - Brash, James T
AU - Campi, Riccardo
AU - Chilelli, Andrew
AU - Conover, Mitchell
AU - Constantinovici, Niculae
AU - Davies, Eleanor
AU - De Meulder, Bertrand
AU - Eid, Sherrine
AU - Gacci, Mauro
AU - Golozar, Asieh
AU - Hafeez, Haroon
AU - Haque, Samiul
AU - Hijazy, Ayman
AU - Hulsen, Tim
AU - Josefsson, Andreas
AU - Khalid, Sara
AU - Kolde, Raivo
AU - Kotik, Daniel
AU - Kurki, Samu
AU - Lambrecht, Mark
AU - Leung, Chi-Ho
AU - Moreno, Julia
AU - Nicoletti, Rossella
AU - Nieboer, Daan
AU - Oja, Marek
AU - Palanisamy, Soundarya
AU - Prinsen, Peter
AU - Reich, Christian
AU - Raffaele Resta, Giulio
AU - Ribal, Maria J
AU - Gómez Rivas, Juan
AU - Smith, Emma
AU - Snijder, Robert
AU - Steinbeisser, Carl
AU - Vandenberghe, Frederik
AU - Cornford, Philip
AU - Evans-Axelsson, Susan
AU - N'Dow, James
AU - Willemse, Peter-Paul M
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/5
Y1 - 2024/5
N2 - Combination therapies in metastatic hormone-sensitive prostate cancer (mHSPC), which include the addition of an androgen receptor signaling inhibitor and/or docetaxel to androgen deprivation therapy, have been a game changer in the management of this disease stage. However, these therapies come with their fair share of toxicities and side effects. The goal of this observational study is to report drug-related adverse events (AEs), which are correlated with systemic combination therapies for mHSPC. Determining the optimal treatment option requires large cohorts to estimate the tolerability and AEs of these combination therapies in "real-life" patients with mHSPC, as provided in this study. We use a network of databases that includes population-based registries, electronic health records, and insurance claims, containing the overall target population and subgroups of patients defined by unique certain characteristics, demographics, and comorbidities, to compute the incidence of common AEs associated with systemic therapies in the setting of mHSPC. These data sources are standardised using the Observational Medical Outcomes Partnership Common Data Model. We perform the descriptive statistics as well as calculate the AE incidence rate separately for each treatment group, stratified by age groups and index year. The time until the first event is estimated using the Kaplan-Meier method within each age group. In the case of episodic events, the anticipated mean cumulative counts of events are calculated. Our study will allow clinicians to tailor optimal therapies for mHSPC patients, and they will serve as a basis for comparative method studies.
AB - Combination therapies in metastatic hormone-sensitive prostate cancer (mHSPC), which include the addition of an androgen receptor signaling inhibitor and/or docetaxel to androgen deprivation therapy, have been a game changer in the management of this disease stage. However, these therapies come with their fair share of toxicities and side effects. The goal of this observational study is to report drug-related adverse events (AEs), which are correlated with systemic combination therapies for mHSPC. Determining the optimal treatment option requires large cohorts to estimate the tolerability and AEs of these combination therapies in "real-life" patients with mHSPC, as provided in this study. We use a network of databases that includes population-based registries, electronic health records, and insurance claims, containing the overall target population and subgroups of patients defined by unique certain characteristics, demographics, and comorbidities, to compute the incidence of common AEs associated with systemic therapies in the setting of mHSPC. These data sources are standardised using the Observational Medical Outcomes Partnership Common Data Model. We perform the descriptive statistics as well as calculate the AE incidence rate separately for each treatment group, stratified by age groups and index year. The time until the first event is estimated using the Kaplan-Meier method within each age group. In the case of episodic events, the anticipated mean cumulative counts of events are calculated. Our study will allow clinicians to tailor optimal therapies for mHSPC patients, and they will serve as a basis for comparative method studies.
U2 - 10.1016/j.euros.2024.02.019
DO - 10.1016/j.euros.2024.02.019
M3 - Article
C2 - 38572301
SN - 2666-1691
VL - 63
SP - 81
EP - 88
JO - European Urology Open Science
JF - European Urology Open Science
ER -