• 生存期整体比较无统计学意义

    OS: P value demonstrated does not have the significance statistics difference.

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  • 生存期会议提交

    Overall survival will be presented at the time of the meeting.

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  • 主要终点指标生存期,资料分析采用意向处理分析。

    The primary endpoint was overall survival, and analysis was done by intention to treat.

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  • 治疗组的无进展生存生存期都没有明显差异

    Neither progression-free survival nor overall survival differed significantly between the treatment arms.

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  • 【译】转移性直肠癌影响生存KRAS测试吗?

    Does KRAS Testing in Metastatic Colorectal Cancer Impact Overall Survival?

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  • 研究人员提到,在生存无进展生存没有差异

    Overall survival and progression-free survival also did not differ in the two groups, the researchers note.

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  • 首要观察终点生存(OS)改为无进展生存期(PFS)。

    The primary end point was amended from overall survival (OS) to progression-free survival (PFS).

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  • 次要终点包括IRC评估的生存期(OS)缓解(ORR)。

    Secondary end points included overall survival (OS) and overall response rate (ORR) per IRC.

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  • 目的观察剂量密度化疗治疗乳腺癌不良反应及对无生存生存期的影响。

    Objective to investigate the adverse effect, disease free survival and overall survival of dose-dense chemotherapy in postoperative breast cancer patients.

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  • 主要指标生存次要指标包括无进展生存期(PFS)客观反应(ORR)。

    The primary endpoint was overall survival, and secondary endpoints included PFS and objective response rate (ORR).

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  • 中位生存期次要观察终点联合为20.5药治疗组为20.6个月。

    But median overall survival, a secondary end point, was 20.5 months in the combination group and 20.6 months in the monotherapy group.

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  • 次要观察终点包括生存期安全性患者对治疗设施满意度理解以及医疗资源利用

    Secondary endpoints included overall survival, safety, patients' satisfaction with and perception of treatment convenience, and medical resource utilization.

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  • 结果FOXP3肿瘤细胞中的表达生存期有关,而且增加了FOXP3免疫染色强度。

    Results: FOXP3 expression in tumors was associated with worse overall survival probability and the risk increased with increasing FOXP3 immunostaining intensity.

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  • 欧美权威机构接受PFS作为观察终点生存期OS),细胞作为贝伐单适应症范围。

    PFS, rather than overall survival (OS), was accepted by regulatory authorities in the United States and Europe as the endpoint for approval of bevacizumab for the renal cell carcinoma indication.

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  • 结论我们对边缘区淋巴瘤研究报道的研究中规模最大之一,结论是边缘区淋巴瘤预后良好总生存期超过19

    Conclusions: In our MZL series, one of the largest reported, prognosis of MZL is good with a median OS of over 19 years.

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  • 二级终点包含了目标反应,一年生存期生存化疗类型安全性PFS评估

    Secondary endpoints included objective response rate, one-year survival rate, overall survival, PFS assessment by chemotherapy type and safety.

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  • 生存反映了生存曲线一个时间不能测量生存期

    Median survival reflects one time point along the survival curve and does not measure the overall survival benefit.

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  • 结果33个被评估病人中,反应为70%(完全反应率加未确定的完全反应率,45%),无进展生存16.5个月

    Results: of 33 evaluated patients, a 70% overall response rate (complete response plus complete response unconfirmed, 45%) and a median progression-free survival (PFS) of 16.5 months were achieved.

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  • 结果33个被评估病人中,反应为70%(完全反应率加未确定的完全反应率,45%),无进展生存16.5个月

    Results: of 33 evaluated patients, a 70% overall response rate (complete response plus complete response unconfirmed, 45%) and a median progression-free survival (PFS) of 16.5 months were achieved.

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