奥拉帕尼
医学
肿瘤科
耐受性
PARP抑制剂
内科学
卵巢癌
BRCA突变
临床终点
浆液性卵巢癌
临床试验
癌症
不利影响
聚ADP核糖聚合酶
聚合酶
化学
基因
生物化学
作者
Panagiotis A. Konstantinopoulos,Antonio González-Martı́n,Felipe Melo Cruz,Michael Friedlander,Rosalind Glasspool,Domenica Lorusso,Christian Marth,Bradley J. Monk,Jae‐Weon Kim,Patsy Hinson,Olga Ajipa,Vincent Prêtre,Yu Han,Ursula A. Matulonis
出处
期刊:Future Oncology
[Future Medicine]
日期:2022-09-06
卷期号:18 (31): 3481-3492
被引量:13
标识
DOI:10.2217/fon-2022-0666
摘要
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- BRCA-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 BRCA mutation. Progression-free survival (blinded independent review committee) is the primary end point. Overall survival is a key secondary end point. Clinical Trial Registration:: NCT04729387 ( ClinicalTrials.gov )
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