TripleAiM1: a nationwide registry of de novo metastatic hormone-sensitive prostate cancer with prospective quality-of-life assessment

Author:

van Elst TessaORCID,van Basten Jean-Paul,van den Berg Pieter,van den Bergh Roderick,Bloem Sjaak,van Dodewaard-de Jong Joyce,Hendriks MathijsORCID,Klaver Sjoerd,Lalmahomed Zarina,Luijendijk Daphne,van de Luijtgaarden Addy,Roelofs Luc,Vis André,Vreugdenhil Gerard,Vrijhof Eric,Wijsman Bart,Bloemendal Haiko,Mulders Peter,Mehra Niven

Abstract

IntroductionThe treatment landscape forde novometastatic hormone sensitive prostate cancer (mHSPC) is rapidly evolving. With an abundance of available treatment strategies, selecting the optimal strategy for an individual patient is becoming increasingly challenging. TripleAiM1 aims to evaluate the impact of mHSPC treatments on health-related quality of life (HRQoL) and to provide real-world data insights on diagnostics, treatment strategies, patient subgroups and related healthcare expenditure for mHSPC. The aspirational target of TripleAiM1 is that in the near future, a more tailored therapy can be offered based on the individual patient’s wishes and needs in accordance with the overarching principle of value-based healthcare.Methods and analysisWe describe the TripleAiM1 study design; a nationwide registry comprising a retrospective and prospective cohort of patients withde novomHSPC. Starting in May 2020, eligible patients are identified, selected and recruited in 14 participating hospitals in the Netherlands. Our hypothesis is that, in a real-world setting, differences in clinically meaningful HRQoL deterioration will be observed for treatment strategies over time. HRQoL data, assessed with patient-reported outcome measures, costs and clinical data will be collected for 24 months.For the retrospective cohort, all patients diagnosed withde novomHSPC from January 2017 onwards are eligible for inclusion. Patient and tumour characteristics, imaging modalities and treatment patterns will be analysed descriptively to provide a real-world overview.Time-to-event endpoints will be assessed using the Kaplan-Meier method and regression models will be employed to analyse baseline characteristics associated with an increased likelihood of death, progression and HRQoL deterioration. Longitudinal mixed-effects models will be employed to assess change of patient-reported outcome scores from baseline until the end of follow-up.Ethics and disseminationEthical approval was obtained from the Medical Research Ethics Committee, Twente. Study results will be published in peer-reviewed journals.Trial registration numberNL9719.

Funder

Janssen-Cilag

Publisher

BMJ

Subject

General Medicine

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