UCL Cancer Trials Centre, London, UK.
Ann Oncol. 2013 Dec;24(12):3028-34. doi: 10.1093/annonc/mdt406. Epub 2013 Nov 4.
The majority of women with ovarian cancer develop recurrent disease. For patients with a platinum-free interval of >6 months, platinum-based chemotherapy is a treatment of choice. The benefit of platinum-based combination chemotherapy in randomized trials varies, and a meta-analysis was carried out to gain more secure information on the size of the benefit of this treatment.
We initiated a systematic review and meta-analysis following a pre-specified protocol to determine whether combination chemotherapy is superior to single-agent platinum chemotherapy in women with relapsed platinum-sensitive ovarian cancer.
A total of five potentially eligible randomized trials were identified that had used combination-platinum chemotherapy versus single-agent platinum chemotherapy in women with relapsed platinum-sensitive ovarian cancer. For one trial (190 patients), adequate contact with the investigators could not be established. Therefore, four trials that randomly assigned 1300 patients were included, with a median follow-up of 36.1 months. Overall survival (OS) analyses were based on 865 deaths and demonstrated evidence for the benefit of combination-platinum chemotherapy (HR = 0.80; 95% CI, 0.64-1.00; P = 0.05). Progression-free survival (PFS) analyses were based on 1167 events and demonstrated strong evidence for the benefit of combination-platinum chemotherapy (HR = 0.68; 95% CI, 0.57-0.81; P < 0.001). There was no evidence of a difference in the relative effect of combination-platinum chemotherapy on either OS or PFS in patient subgroups defined by previous paclitaxel (Taxol) treatment (OS, P = 0.49; PFS, P = 0.66), duration of treatment-free interval (OS, P = 0.86; PFS, P = 0.48) or the number of previous lines of chemotherapy (OS, P = 0.21; PFS, P = 0.27).
In this individual patient data (IPD) meta-analysis, we have demonstrated that combination-platinum chemotherapy improves OS and PFS across all subgroups. This provides the strongest evidence to date of the benefit of combination-platinum over single-agent platinum.
大多数卵巢癌患者会出现疾病复发。对于无铂间期>6 个月的患者,铂类药物为基础的化疗是首选治疗方法。随机试验中铂类联合化疗的获益有所不同,因此进行了一项荟萃分析,以获得关于这种治疗获益大小的更可靠信息。
我们按照预先制定的方案进行了系统评价和荟萃分析,以确定在复发性铂类敏感卵巢癌患者中,联合化疗是否优于单药铂类化疗。
共确定了五项可能符合条件的随机试验,这些试验在复发性铂类敏感卵巢癌患者中使用了联合铂类化疗与单药铂类化疗。对于一项试验(190 例患者),无法与研究者取得充分联系。因此,纳入了四项随机分配 1300 例患者的试验,中位随访时间为 36.1 个月。总生存(OS)分析基于 865 例死亡,表明联合铂类化疗有获益(HR=0.80;95%CI,0.64-1.00;P=0.05)。无进展生存(PFS)分析基于 1167 例事件,表明联合铂类化疗有显著获益(HR=0.68;95%CI,0.57-0.81;P<0.001)。在以前用过紫杉醇(Taxol)治疗(OS,P=0.49;PFS,P=0.66)、无铂间期持续时间(OS,P=0.86;PFS,P=0.48)或以前化疗线数(OS,P=0.21;PFS,P=0.27)的亚组患者中,联合铂类化疗的相对疗效无差异的证据。
在这项个体患者数据(IPD)荟萃分析中,我们证明联合铂类化疗可改善所有亚组的 OS 和 PFS。这提供了迄今为止联合铂类药物优于单药铂类药物的最强证据。