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
Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Clínica Universidad de Navarra & Program in Solid Tumors, Center for Applied Medical Research (CIMA), Pamplona, 31008, Spain.
Future Oncol. 2022 Oct;18(31):3481-3492. doi: 10.2217/fon-2022-0666. Epub 2022 Sep 6.
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. : NCT04729387 (ClinicalTrials.gov).
铂耐药或难治性高级别浆液性卵巢癌(HGSOC)患者预后较差,其治疗是一项重大的未满足医疗需求。临床前数据和一项Ib期试验结果表明,α特异性磷脂酰肌醇-3激酶(PI3K)抑制剂阿培利司与聚(腺苷二磷酸-核糖)聚合酶(PARP)抑制剂奥拉帕利联合应用于铂耐药、无BRCA突变的卵巢癌具有疗效和耐受性。在此,我们描述了III期、多中心、开放标签、随机、活性对照EPIK-O/ENGOT-OV61试验的研究设计和原理,该试验旨在研究阿培利司联合奥拉帕利与铂耐药或难治性无胚系突变HGSOC患者的标准护理化疗相比的疗效。无进展生存期(盲法独立审查委员会评估)是主要终点。总生存期是关键的次要终点。试验编号:NCT04729387(ClinicalTrials.gov) 。