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改进中值插补法估计区间删失生存时间数据的中位数生存时间。

Improvement of Midpoint Imputation for Estimation of Median Survival Time for Interval-Censored Time-to-Event Data.

机构信息

Biometrics Department, Chugai Pharmaceutical Co., Ltd., 2-1-1 Nihonbashi-Muromachi, Chuo-Ku, Tokyo, 103-8324, Japan.

Department of Management Science, Graduate School of Engineering, Tokyo University of Science, Tokyo, Japan.

出版信息

Ther Innov Regul Sci. 2024 Jul;58(4):721-729. doi: 10.1007/s43441-024-00640-7. Epub 2024 Apr 10.

Abstract

BACKGROUND

Progression-free survival (PFS) is used to evaluate treatment effects in cancer clinical trials. Disease progression (DP) in patients is typically determined by radiological testing at several scheduled tumor-assessment time points. This produces a discrepancy between the true progression time and the observed progression time. When the observed progression time is considered as the true progression time, a positively biased PFS is obtained for some patients, and the estimated survival function derived by the Kaplan-Meier method is also biased.

METHODS

While the midpoint imputation method is available and replaces interval-censored data with midpoint data, it unrealistically assumes that several DPs occur at the same time point when several DPs are observed within the same tumor-assessment interval. We enhanced the midpoint imputation method by replacing interval-censored data with equally spaced timepoint data based on the number of observed interval-censored data within the same tumor-assessment interval.

RESULTS

The root mean square error of the median of the enhanced method is almost always smaller than that of the midpoint imputation regardless of the tumor-assessment frequency. The coverage probability of the enhanced method is close to the nominal confidence level of 95% in most scenarios.

CONCLUSION

We believe that the enhanced method, which builds upon the midpoint imputation method, is more effective than the midpoint imputation method itself.

摘要

背景

无进展生存期 (PFS) 用于评估癌症临床试验中的治疗效果。患者的疾病进展 (DP) 通常通过在几个预定的肿瘤评估时间点进行影像学检查来确定。这导致真实进展时间与观察到的进展时间之间存在差异。当观察到的进展时间被视为真实的进展时间时,一些患者的 PFS 会得到正向偏倚,并且通过 Kaplan-Meier 方法得出的估计生存函数也会受到偏倚。

方法

虽然中点插补法可用于用中点数据替换区间删失数据,但当在同一肿瘤评估间隔内观察到多个 DP 时,它不合理地假设几个 DP 同时发生。我们通过根据同一肿瘤评估间隔内观察到的区间删失数据的数量,用等间隔时间点数据替换区间删失数据,从而增强了中点插补法。

结果

增强方法的中位数的均方根误差几乎总是小于中点插补法,无论肿瘤评估频率如何。在大多数情况下,增强方法的覆盖率接近名义置信水平 95%。

结论

我们认为,在中点插补法的基础上进行增强的方法比中点插补法本身更有效。

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