Klar M, Hasenburg A, Hasanov M, Hilpert F, Meier W, Pfisterer J, Pujade-Lauraine E, Herrstedt J, Reuss A, du Bois A
Department of Obstetrics and Gynecology, University Clinics of Freiburg, Freiburg, Germany.
Department of Obstetrics and Gynecology, University Clinics of Mainz, Mainz, Germany.
Eur J Cancer. 2016 Oct;66:114-24. doi: 10.1016/j.ejca.2016.07.014. Epub 2016 Aug 23.
We evaluated in a large study meta-database of prospectively randomised phase III trials the prognostic factors for progression-free survival (PFS) and overall survival (OS) in patients < and >40 years of age with advanced epithelial ovarian cancer.
A total of 5055 patients of the AGO, GINECO, NSGO intergroup studies AGO-OVAR 3, 5, 7 and 9 were merged to identify 294 patients <40 years and 4761 patients ≥40 years. We conducted survival analyses and Cox proportional hazard regression models and additionally analysed a very homogeneous subcohort of 405 patients with serous epithelial ovarian cancer, excellent performance status, who had received complete macroscopic upfront cytoreduction and ≥5 chemotherapy cycles.
For patients <40 years, the median PFS was 28.9 months and the median OS was 75.3 months, while the median PFS for patients ≥40 years was 18.1 months and the median OS was 45.7 months. Independent prognostic factors were similar in both age groups. In a multivariate analysis including prognostic factors potentially leading to confounding, young age appeared to improve PFS (hazard ratio [HR], 0.86; 95% confidence interval [CI]: 0.72-1.03) and OS (HR, 0.73; 95% CI: 0.59-0.91). The observed effect was even stronger in the subcohort of optimally treated patients with SEOC: PFS (HR, 0.34; 95% CI: 0.19-0.59) and OS (HR, 0.23; 95% CI: 0.09-0.56).
Prognostic factors were similar in both age groups. Young age appeared a strong independent protective prognostic factor for PFS and OS in the subcohort.
我们在一项前瞻性随机III期试验的大型研究元数据库中,评估了年龄<40岁和≥40岁的晚期上皮性卵巢癌患者无进展生存期(PFS)和总生存期(OS)的预后因素。
合并AGO、GINECO、NSGO协作组研究AGO-OVAR 3、5、7和9的总共5055例患者,以识别出294例年龄<40岁的患者和4761例年龄≥40岁的患者。我们进行了生存分析和Cox比例风险回归模型,并另外分析了405例浆液性上皮性卵巢癌、体能状态良好、接受了完整的宏观术前细胞减灭术且化疗周期≥5个周期的非常同质的亚组。
对于年龄<40岁的患者,中位PFS为28.9个月,中位OS为75.3个月,而年龄≥40岁的患者中位PFS为18.1个月,中位OS为45.7个月。两个年龄组的独立预后因素相似。在包括可能导致混淆的预后因素的多变量分析中,年轻似乎可改善PFS(风险比[HR],0.86;95%置信区间[CI]:0.72-1.03)和OS(HR,0.73;95%CI:0.59-0.91)。在最佳治疗的SEOC患者亚组中观察到的效应更强:PFS(HR,0.34;95%CI:0.19-0.59)和OS(HR,0.23;95%CI:0.09-0.56)。
两个年龄组的预后因素相似。在亚组中,年轻似乎是PFS和OS的一个强大的独立保护性预后因素。