Design for immuno‐oncology clinical trials enrolling both responders and nonresponders-Reference-Cited by-同舟云学术

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Design for immuno‐oncology clinical trials enrolling both responders and nonresponders

Published:2020-09-17 Issue:27 Volume:39 Page:3914-3936
ISSN:0277-6715
Container-title:Statistics in Medicine
language:en
Short-container-title:Statistics in Medicine

Author:

Xu Zhenzhen¹^ORCID,Zhu Bin²,Park Yongsoek³

Affiliation:

1. Center for Biologics Evaluation and Research Food and Drug Administration Silver Spring Maryland USA

2. Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda Maryland USA

3. Department of Biostatistics University of Pittsburgh Pittsburgh Pennsylvania USA

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/sim.8694

Reference45 articles.

1. Designing therapeutic cancer vaccine trials with delayed treatment effect

2. Designing cancer immunotherapy trials with random treatment time‐lag effect

3. Design and analysis of clinical trials in the presence of delayed treatment effect

4. The use of restricted mean survival time to estimate the treatment effect in randomized clinical trials when the proportional hazards assumption is in doubt

5. Augmenting the logrank test in the design of clinical trials in which non-proportional hazards of the treatment effect may be anticipated

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Group sequential design with maximin efficiency robust test for immunotherapy with generalized delayed treatment effect;Pharmaceutical Statistics;2023-10-19

2. M&M: A maximum duration design with the Maxcombo test for a group sequential trial of an immunotherapy with a random delayed treatment effect;Statistics in Medicine;2021-11-15

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