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首页> 外文期刊>The British journal of cancer >Relationship between effects on time-to-disease progression and overall survival in studies of metastatic breast cancer.
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Relationship between effects on time-to-disease progression and overall survival in studies of metastatic breast cancer.

机译:对time-to-disease的影响之间的关系发展和整体生存的研究转移性乳腺癌。

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The relationship between overall survival (OS) and disease progression end points has been demonstrated in colorectal, colon, and non-small cell lung cancers. We assessed the association between OS and time-to-progression (TTP) or progression-free survival (PFS) in metastatic breast cancer (MBC) studies. A literature search retrieved all randomised controlled trials since 1994 in patients with MBC in which OS and either TTP or PFS were reported. Summary data on trial and patient characteristics were abstracted. Study effect sizes were derived as the ratio of median progression (or survival) times, which approximates the hazard ratio. Effects were centred at zero for regression analyses weighted by sample size. Numerous treatments were represented in 67 studies (17 081 patients). Modeling showed a positive association between outcomes for progression and survival (R(2)=0.30) with a slope of 0.32 (P<0.001) and a non-significant intercept. Thus, a treatment effect on TTP/PFS translated into a concordant effect on OS, but with attenuated effect size. Similar results were found in models of subsets and sensitivity analyses. These results demonstrate that treatment effects on progression end points in MBC trials are expected to result in treatment differences on OS that are smaller yet consistently in the same direction.
机译:总生存期(OS)和之间的关系疾病进展的结束点在结直肠、结肠和非小细胞肺癌。操作系统和time-to-progression (TTP)之间无进展生存(PFS)的转移乳腺癌(MBC)研究。检索所有的随机对照试验1994年在MBC OS和患者TTP或PFS报道。和病人的特点是抽象的。研究尺度效应是派生的比率中位(或进展生存期)时代,这接近风险比。集中在零加权回归分析样本大小。代表67年研究(17 081名患者)。建模显示积极的联系结果发展和生存(R (2) = 0.30)斜率为0.32 (P < 0.001)非重要拦截。影响TTP / PFS译成一个整合影响操作系统,但减毒效果。也发现类似的结果模型的子集和敏感性分析。证明治疗对发展的影响结束点在MBC试验预计的结果在治疗差异较小的操作系统然而始终在同一个方向。

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