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Bibliographic Details
Main Authors: Iijima, Takuto, Momozaki, Tomotaka, Ando, Shuji
Format: Preprint
Published: 2025
Subjects:
Online Access:https://arxiv.org/abs/2502.20011
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author Iijima, Takuto
Momozaki, Tomotaka
Ando, Shuji
author_facet Iijima, Takuto
Momozaki, Tomotaka
Ando, Shuji
contents In recent years, cancer clinical trials have increasingly encountered non proportional hazards (NPH) scenarios, particularly with the emergence of immunotherapy. In randomized controlled trials comparing immunotherapy with conventional chemotherapy or placebo, late difference and early crossing survivals scenarios are commonly observed. In such cases, window mean survival time (WMST), the area under the survival curve within a pre-specified interval $[τ_0, τ_1]$, has gained increasing attention due to its superior power compared to restricted mean survival time (RMST), the area under the survival curve up to a pre-specified time point. Considering the increasing use of progression-free survival as a co-primary endpoint alongside overall survival, there is a critical need to establish a WMST estimation method for interval-censored data; however, sufficient research has yet to be conducted. To bridge this gap, this study proposes a WMST inference method utilizing one-point imputations and Turnbull's method. Extensive numerical simulations demonstrate that the WMST estimation method using mid-point imputation for interval-censored data exhibits comparable performance to that using Turnbull's method. Since the former facilitates standard error calculation, we adopt it as the standard method. Numerical simulations on two-sample tests confirm that the proposed WMST testing method have higher power than RMST in late difference and early crossing survival scenarios, while having compatible power to the log-rank test under the PH. Furthermore, even when pre-specified $τ_0$ deviated from the clinically desirable time point, WMST consistently maintains higher power than RMST in late difference and early crossing survivals scenarios.
format Preprint
id arxiv_https___arxiv_org_abs_2502_20011
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle On window mean survival time with interval-censored data
Iijima, Takuto
Momozaki, Tomotaka
Ando, Shuji
Applications
In recent years, cancer clinical trials have increasingly encountered non proportional hazards (NPH) scenarios, particularly with the emergence of immunotherapy. In randomized controlled trials comparing immunotherapy with conventional chemotherapy or placebo, late difference and early crossing survivals scenarios are commonly observed. In such cases, window mean survival time (WMST), the area under the survival curve within a pre-specified interval $[τ_0, τ_1]$, has gained increasing attention due to its superior power compared to restricted mean survival time (RMST), the area under the survival curve up to a pre-specified time point. Considering the increasing use of progression-free survival as a co-primary endpoint alongside overall survival, there is a critical need to establish a WMST estimation method for interval-censored data; however, sufficient research has yet to be conducted. To bridge this gap, this study proposes a WMST inference method utilizing one-point imputations and Turnbull's method. Extensive numerical simulations demonstrate that the WMST estimation method using mid-point imputation for interval-censored data exhibits comparable performance to that using Turnbull's method. Since the former facilitates standard error calculation, we adopt it as the standard method. Numerical simulations on two-sample tests confirm that the proposed WMST testing method have higher power than RMST in late difference and early crossing survival scenarios, while having compatible power to the log-rank test under the PH. Furthermore, even when pre-specified $τ_0$ deviated from the clinically desirable time point, WMST consistently maintains higher power than RMST in late difference and early crossing survivals scenarios.
title On window mean survival time with interval-censored data
topic Applications
url https://arxiv.org/abs/2502.20011