Division of Medical Oncology, Department of Uro-Gynaecological Oncology, Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale," Naples, Italy.
Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, Essen, Germany.
Ann Oncol. 2017 Nov 1;28(suppl_8):viii51-viii56. doi: 10.1093/annonc/mdx441.
Despite optimal surgery and appropriate first-line chemotherapy, ∼70%-80% of patients with epithelial ovarian cancer will develop disease relapse. The same modalities as used primarily are available for treatment of recurrent ovarian cancer (ROC). The rationale for repetitive surgery in ROC was based on a stable body of retrospective data; however, prospective data were missing. Now, preliminary data from the prospective AGO-DESKTOP III give evidence that surgery for ROC seems to be of benefit for selected patients with platinum-sensitive relapse undergoing complete resection. With respect to systemic therapy, tumor histology, BRCA status, the platinum-free interval (PFI) and previous treatment with bevacizumab (anti-VEGF monoclonal antibody) are considered the most important features that influence treatment choice in ROC. In patients with resistant or refractory relapse (PFI < 6 months), monotherapy with a non-platinum drug or participation in clinical trials is indicated. The association of non-platinum monotherapy with bevacizumab, followed by maintenance has been approved in this setting in some European countries due to PFS benefit. In patients with partially sensitive relapse (PFI between 6 and 12 months), two options are available: platinum doublets or non-platinum therapy (single agent or combination). The pegylated liposomal doxorubicin/trabectedin combination represents a viable alternative in patients that cannot receive platinum. In platinum-sensitive patients, treatment with platinum-based combinations is associated with PFS advantage compared with single agents or non-platinum combinations. The presence of germline or somatic BRCA mutations allows platinum-responsive patients to optimize chemotherapy efficacy and prolonging PFS by the use of olaparib (PARP inhibitor) given as maintenance therapy until progression. In patients not pretreated with bevacizumab in first line, the carboplatin/gemcitabine/bevacizumab combination, followed by maintenance is a viable alternative in platinum-sensitive patients (PFI> 6 months). The integration of surgery, with a 'personalized' approach by the use of antiangiogenic agent and of PARP inhibitors is affecting survival of patients with recurrent disease and will help epithelial ovarian cancer to become a chronic disease.
尽管进行了最佳的手术和适当的一线化疗,约 70%-80%的上皮性卵巢癌患者仍会出现疾病复发。同样的治疗方法也可用于复发性卵巢癌 (ROC) 的治疗。在 ROC 中反复手术的依据是基于大量稳定的回顾性数据;然而,缺乏前瞻性数据。现在,来自前瞻性 AGO-DESKTOP III 的初步数据表明,对于接受完全切除的铂类敏感复发患者,手术似乎对某些患者有益。关于系统治疗,肿瘤组织学、BRCA 状态、无铂间隔(PFI)和贝伐单抗(抗 VEGF 单克隆抗体)的先前治疗被认为是影响 ROC 治疗选择的最重要特征。对于耐药或难治性复发患者(PFI<6 个月),建议使用非铂类药物单药治疗或参加临床试验。由于无进展生存期(PFS)获益,在一些欧洲国家,铂类药物单药联合贝伐单抗,然后进行维持治疗已被批准用于该治疗方案。对于部分敏感复发患者(PFI 介于 6 至 12 个月之间),有两种选择:铂类双联或非铂类治疗(单药或联合)。聚乙二醇脂质体阿霉素/曲贝替定联合治疗对于不能接受铂类药物的患者是一种可行的替代方案。在铂类敏感患者中,与单药治疗或非铂类联合治疗相比,铂类药物联合治疗与 PFS 优势相关。生殖系或体细胞 BRCA 突变的存在使铂类反应性患者能够通过使用奥拉帕利(PARP 抑制剂)进行维持治疗来优化化疗效果并延长 PFS,直到疾病进展。在一线治疗中未使用贝伐单抗的患者中,卡铂/吉西他滨/贝伐单抗联合治疗,然后进行维持治疗是铂类敏感患者的一种可行选择(PFI>6 个月)。手术与通过使用抗血管生成药物和 PARP 抑制剂的“个体化”方法相结合,正在影响复发性疾病患者的生存,并将有助于将上皮性卵巢癌转变为慢性疾病。