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首页> 外文期刊>Molecular biology reports >Toremifene and tamoxifen have similar efficacy in the treatment of patients with breast cancer: a meta-analysis of randomized trials
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Toremifene and tamoxifen have similar efficacy in the treatment of patients with breast cancer: a meta-analysis of randomized trials

机译:托瑞米芬和他莫昔芬在治疗乳腺癌患者中具有相似的功效:一项随机试验的荟萃分析

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A meta-analysis of randomized trials was performed to compare the efficacy of toremifene (TOR) with tamoxifen (TAM) in patients with breast cancer. A total of 4,768 intention-to-treat patients from nine randomized trials were identified, with 2,587 patients in TOR group and 2,181 patients in TAM group. The primary outcomes were objective response rate (ORR), time to progression (TTP), and overall survival (OS). The ORR for TOR group was 26.2 % (303/1,156), whereas the ORR for TAM group was 25.2 % (284/1,128). The pooled RR suggested that the ORR were not statistically different between the two therapeutic groups (RR 1.04, 95 % CI 0.91-1.20, P = 0.57). The median TTP was 6.7 months for the TOR group and 9.7 months for the TAM group. The median OS was 30.1 months for the TOR group and 31.7 months for the TAM group. There were no significant difference in TTP and OS between two therapeutic groups (for TTP: HR 0.91, 95 % CI 0.82-1.00; for OS: HR 1.02, 95 % CI 0.91-1.15). Adverse events were generally similar in two therapeutic groups, but TOR may cause fewer vaginal bleeding (4.0 vs. 6.7 %, P < 0.01), headache (0.2 vs. 3.1 %, P = 0.02) and thromboembolic events (4.7 vs. 7.0 %, P = 0.04). Sensitivity analyses were performed by deleting a single study each time; all the results were not materially altered. In summary, the results of this meta-analysis suggest that TOR and TAM have similar efficacy in the treatment of patients with breast cancer.
机译:进行了一项随机试验的荟萃分析,以比较托瑞米芬(TOR)和他莫昔芬(TAM)在乳腺癌患者中的疗效。从9项随机试验中,总共鉴定出4768名意向治疗患者,其中TOR组为2587例,TAM组为2181例。主要结果是客观缓解率(ORR),进展时间(TTP)和总生存期(OS)。 TOR组的ORR为26.2%(303 / 1,156),而TAM组的ORR为25.2%(284 / 1,128)。合并的RR提示两个治疗组之间的ORR在统计学上没有差异(RR 1.04,95%CI 0.91-1.20,P = 0.57)。 TOR组的中位TTP为6.7个月,TAM组的中位TTP为9.7个月。 TOR组的中位OS为30.1个月,TAM组的中位OS为31.7个月。两个治疗组之间的TTP和OS没有显着差异(对于TTP:HR 0.91,95%CI 0.82-1.00;对于OS:HR 1.02,95%CI 0.91-1.15)。在两个治疗组中,不良事件通常相似,但TOR可能导致较少的阴道出血(4.0 vs. 6.7%,P <0.01),头痛(0.2 vs. 3.1%,P = 0.02)和血栓栓塞事件(4.7 vs. 7.0%) ,P = 0.04)。通过每次删除单个研究进行敏感性分析;所有结果均未发生重大变化。总而言之,这项荟萃分析的结果表明,TOR和TAM在乳腺癌患者的治疗中具有相似的功效。

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