Oncology Unit, Department of Clinical Therapeutics, Alexandra Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.
1st Department of Obstetrics and Gyencology, Alexandra Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.
Curr Oncol. 2021 Nov 3;28(6):4446-4456. doi: 10.3390/curroncol28060377.
High grade serous ovarian carcinoma (HGSOC) is the most lethal type of epithelial ovarian cancer, with a prevalence of germline mutations as high as 20%. Our objective is to determine whether the location of mutations in the different domains of the genes affects the clinical outcome of HGSOC patients.
A total of 51 women with or mutated ovarian cancer were identified. Progression-free survival (PFS) and overall survival (OS) were analyzed.
In our study cohort, 35 patients were carriers of germline mutations in and 16 in . The median PFS time following completion of the primary therapy was 23.8 months (95% CI 20.1-27.5) and the median OS was 92.9 months (95% CI 69.8-116.1) in all carriers. After multivariate analysis, no significant association among the location or type of mutation with PFS or OS was identified. Notably, significant differences in PFS between carriers of identical mutations in the same gene were detected.
Among HGSOC patients, carriers with mutations in different locations of the genes show no significant difference in survival outcomes, in terms of PFS and OS, suggesting the potential effect of other genetic abnormalities and co-contributing risk factors.
高级别浆液性卵巢癌(HGSOC)是最致命的上皮性卵巢癌类型,种系突变的患病率高达 20%。我们的目的是确定基因不同结构域突变的位置是否会影响 HGSOC 患者的临床结局。
共确定了 51 名携带或突变的卵巢癌患者。分析无进展生存期(PFS)和总生存期(OS)。
在我们的研究队列中,35 名患者携带种系突变,16 名患者携带突变。所有携带者完成初始治疗后的中位 PFS 时间为 23.8 个月(95%CI 20.1-27.5),中位 OS 为 92.9 个月(95%CI 69.8-116.1)。多因素分析后,未发现突变位置或类型与 PFS 或 OS 之间存在显著相关性。值得注意的是,在同一基因中携带相同突变的携带者之间,PFS 存在显著差异。
在 HGSOC 患者中,基因不同位置携带突变的携带者在 PFS 和 OS 方面的生存结局无显著差异,提示存在其他遗传异常和共同的致病因素的潜在影响。