Platinum versus platinum-combination chemotherapy in platinum-sensitive recurrent ovarian cancer: a meta-analysis using individual patient data

被引:66
作者
Raja, F. A. [1 ]
Counsell, N. [1 ]
Colombo, N. [2 ]
Pfisterer, J. [3 ]
du Bois, A. [4 ]
Parmar, M. K. [5 ]
Vergote, I. B. [6 ]
Gonzalez-Martin, A. [7 ]
Alberts, D. S. [8 ]
Plante, M. [9 ]
Torri, V. [10 ]
Ledermann, J. A. [1 ]
机构
[1] UCL Canc Trials Ctr, London WT1 4TJ, England
[2] Univ Milano Bicocca, Milan, Italy
[3] Klinikum Solingen, Klin Gyakol & Geburtshife Stadt, Solingen, Germany
[4] Horst Schmidt Klin, Dept Gynecol & Gynecol Oncol, Wiesbaden, Germany
[5] MRC, Clin Trials Unit, London, England
[6] Univ Louvain, Div Gynaecol Oncol, Louvain, Belgium
[7] MD Andersen Canc Ctr, Madrid, Spain
[8] Univ Arizona, Ctr Canc, Tucson, AZ 85721 USA
[9] Univ Laval, Quebec City, PQ, Canada
[10] Mario Negri Inst Pharmacol Res, Milan, Italy
关键词
IPD meta-analysis; recurrent ovarian cancer; PHASE-III TRIAL; EPITHELIAL OVARIAN; PLUS CARBOPLATIN; OPEN-LABEL; CARCINOMA; THERAPY; PACLITAXEL; CISPLATIN; PERITONEAL; OLAPARIB;
D O I
10.1093/annonc/mdt406
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:3028 / 3034
页数:7
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