EPIK-O/ENGOT-OV61: alpelisib plus olaparib vs cytotoxic chemotherapy in high-grade serous ovarian cancer (phase III study)

Patients with platinum-resistant or -refractory high-grade serous ovarian cancer (HGSOC) have a poor prognosis, and their management represents a substantial unmet medical need. Preclinical data and results from a phase Ib trial demonstrated the efficacy and tolerability of the combination of the α-...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Future oncology (London, England) England), 2022-10, Vol.18 (31), p.3481-3492
Hauptverfasser: Konstantinopoulos, Panagiotis A, Gonzalez-Martin, Antonio, Cruz, Felipe Melo, Friedlander, Michael, Glasspool, Rosalind, Lorusso, Domenica, Marth, Christian, Monk, Bradley J, Kim, Jae-Weon, Hinson, Patsy, Ajipa, Olga, Pretre, Vincent, Han, Yu, Matulonis, Ursula A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Patients with platinum-resistant or -refractory high-grade serous ovarian cancer (HGSOC) have a poor prognosis, and their management represents a substantial unmet medical need. Preclinical data and results from a phase Ib trial demonstrated the efficacy and tolerability of the combination of the α-specific phosphatidylinositol-3-kinase (PI3K) inhibitor alpelisib plus the poly(adenosine diphosphate-ribose) polymerase (PARP) inhibitor olaparib in platinum-resistant, non- -mutated ovarian cancer. Here, we describe the study design and rationale for the phase III, multicenter, open-label, randomized, active-controlled EPIK-O/ENGOT-OV61 trial investigating alpelisib in combination with olaparib compared with standard-of-care chemotherapy in patients with platinum-resistant or -refractory HGSOC with no germline mutation. Progression-free survival (blinded independent review committee) is the primary end point. Overall survival is a key secondary end point. : ( )
ISSN:1479-6694
1744-8301
DOI:10.2217/fon-2022-0666