BOOG
Dr. V.O. Dezentjé (NKI-AvL), dr. I.R.H.M. Konings (Amsterdam UMC), dr. M.M.E.M. Bos (Erasmus MC)
Dr. S.M. van den Berg (BOOG Study Center)
Annemarie Almekinders NKI-AvL. E: sequel@nki.nl, T: 020-512 2439
NKI Data Center
NKI Data Center
Centrum zelf of IKNL
Novartis
Multicenter, single arm phase II trial
Admiraal de Ruyter Ziekenhuis | Máxima Medisch Centrum |
Amphia Ziekenhuis | Meander Medisch Centrum |
Amsterdam UMC | Medisch Centrum Leeuwarden |
Antoni van Leeuwenhoek ziekenhuis | Medisch Spectrum Twente |
Canisius Wilhelmina Ziekenhuis | Noordwest Ziekenhuisgroep |
Deventer ziekenhuis | Reinier de Graaf Gasthuis |
Elisabeth-TweeSteden Ziekenhuis | Rijnstate Ziekenhuis |
Franciscus Gasthuis & Vlietland | Spaarne Gasthuis |
Gelre Ziekenhuizen | St. Antonius Ziekenhuis |
Haga Ziekenhuis | Viecuri Medisch Centrum |
Jeroen Bosch Ziekenhuis | Ziekenhuis Amstelland |
Maasstad Ziekenhuis | Ziekenhuisgroep Twente |
Martini Ziekenhuis |
To investigate the efficacy of the combination of fulvestrant and alpelisib directly after progression on 1st or 2nd line therapy with fulvestrant in patients pretreated with a CDK 4/6 inhibitor (in first or secondline) in pre- or postmenopausal women and men with HR+HER2- advanced breast cancer with tumors harboring an activating PIK3CA mutation. Primary endpoint is PFS. The aim is to determine a clinically meaningful median PFS of at least six months.
Primary endpoint:
To determine Progression-free survival (PFS), defined as time from study enrollment to disease progression or death from any cause, with censoring when fulvestrant and alpelisib are stopped and another treatment is initiated without confirmed disease progression.
Secondary endpoints:
The most important inclusion criteria are: