Searcharxiv⌕ Search

arXiv subjects

Madhu Mazumdar

Publications and source records attributed to Madhu Mazumdar.

2 recordsLinked to original sources

Continuous monitoring of delayed outcomes in basket trials

Precision medicine has led to a paradigm shift allowing the development of targeted drugs that are agnostic to the tumor location. In this context, basket trials aim to identify which tumor types - or baskets - would benefit from the targeted therapy among patients with the same molecular marker or mutation. We propose the implementation of continuous monitoring for basket trials to increase the likelihood of early identification of non-promising baskets. Although the current Bayesian trial designs available in the literature can incorporate more than one interim analysis, most of them have high computational cost, and none of them handle delayed outcomes that are expected for targeted treatments such as immunotherapies. We leverage the Bayesian empirical approach proposed by Fujiwara et al., which has low computational cost. We also extend ideas of Cai et al to address the practical challenge of performing interim analysis with delayed outcomes using multiple imputation. Operating characteristics of four different strategies to handle delayed outcomes in basket trials are compared in an extensive simulation study with the benchmark strategy where trial accrual is put on hold until complete data is observed to make a decision. The optimal handling of missing data at interim analyses is trial-dependent. With slow accrual, missingness is minimal even with continuous monitoring, favoring simpler approaches over computationally intensive methods. Although individual sample-size savings are small, multiple imputation becomes more appealing when sample size savings scale with the number of baskets and agents tested.

stat.ME↗

Intra-Class Correlation Coefficient Ignorable Clustered Randomized Trials for Detecting Treatment Effect Heterogeneity

Accurately estimating the intra-class correlation coefficient (ICC) is crucial for adequately powering clustered randomized trials (CRTs). Challenges arise due to limited prior data on the specific outcome within the target population, making accurate ICC estimation difficult. Furthermore, ICC can vary significantly across studies, even for the same outcome, influenced by factors like study design, participant characteristics, and the specific intervention. Power calculations are extremely sensitive to ICC assumptions. Minor variation in the assumed ICC can lead to large differences in the number of clusters needed, potentially impacting trial feasibility and cost. This paper identifies a special class of CRTs aiming to detect the treatment effect heterogeneity, wherein the ICC can be completely disregarded in calculation of power and sample size. This result offers a solution for research projects lacking preliminary estimates of the ICC or facing challenges in their estimate. Moreover, this design facilitates power improvement through increasing the cluster sizes rather than the number of clusters, making it particular advantageous in the situations where expanding the number of clusters is difficult or costly. This paper provides a rigorous theoretical foundation for this class of ICC-ignorable CRTs, including mathematical proofs and practical guidance for implementation. We also present illustrative examples to demonstrate the practical implications of this approach in various research contexts in healthcare delivery.

stat.ME↗