Department of Obstetrics and Gynecology, Korea University Medical Center, Seoul, Republic of Korea.
Department of Obstetrics and Gynecology, Seoul National University Hospital, Seoul, Republic of Korea.
In Vivo. 2024 May-Jun;38(3):1338-1350. doi: 10.21873/invivo.13574.
BACKGROUND/AIM: Over the past several decades, new anti-cancer drugs have been developed for the treatment of epithelial ovarian cancer. The development of drugs has led to changes in improving the prognosis of ovarian cancer patients. One of these drugs, bevacizumab, is used for advanced or recurrent ovarian cancer. In this study, we aimed to evaluate survival improvement in patients with platinum-resistant relapsed epithelial ovarian cancer (PR-ROC) after introduction of bevacizumab in real world experience.
We retrospectively divided patients with PR-ROC into two groups: bevacizumab plus chemotherapy (BEV-CT group) and chemotherapy alone (CT group). Progression-free survival (PFS), the primary endpoint, between two groups was compared to evaluate whether survival outcomes were improved. In addition, overall survival (OS) was also compared.
A total of 154 patients were included in the study: 57 and 97 patients in the BEV-CT and CT groups, respectively. OS was significantly longer in the BEV-CT group than in the CT group. The use of bevacizumab was identified as a favorable prognostic factor for OS. In a subgroup analysis confined to second-line chemotherapy, PFS and OS were statistically different between groups. More patients in the CT group suffered hematologic adverse events of grade 3 or above than patients in the BEV-CT group.
In a real-world clinical setting, introduction of bevacizumab led to improvement of OS in patients with PR-ROC with a tolerable toxicity.
背景/目的:在过去几十年中,已经开发出许多新的抗癌药物来治疗上皮性卵巢癌。药物的发展改变了提高卵巢癌患者预后的方式。其中一种药物贝伐珠单抗(bevacizumab)用于治疗晚期或复发性卵巢癌。在本研究中,我们旨在评估贝伐珠单抗引入真实世界经验后,铂耐药复发性上皮性卵巢癌(PR-ROC)患者的生存改善情况。
我们回顾性地将 PR-ROC 患者分为两组:贝伐珠单抗联合化疗(BEV-CT 组)和单纯化疗(CT 组)。比较两组之间的无进展生存期(PFS),即主要终点,以评估生存结果是否得到改善。此外,还比较了总生存期(OS)。
共有 154 名患者纳入研究:BEV-CT 组和 CT 组分别为 57 例和 97 例。BEV-CT 组的 OS 明显长于 CT 组。贝伐珠单抗的使用被确定为 OS 的有利预后因素。在仅限于二线化疗的亚组分析中,两组之间的 PFS 和 OS 存在统计学差异。CT 组发生 3 级或以上血液学不良事件的患者多于 BEV-CT 组。
在真实临床环境中,贝伐珠单抗的引入导致铂耐药复发性上皮性卵巢癌患者的 OS 得到改善,且毒性可耐受。