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Marcio A. Diniz

Publications and source records attributed to Marcio A. Diniz.

4 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.

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Modeling synergism in early phase cancer trials with drug combination with continuous dose levels: is there an added value?

In parametric Bayesian designs of early phase cancer clinical trials with drug combinations exploring a discrete set of partially ordered doses, several authors claimed that there is no added value in including an interaction term to model synergism between the two drugs. In this paper, we investigate these claims in the setting of continuous dose levels of the two agents. Parametric models will be used to describe the relationship between the doses of the two agents and the probability of dose limiting toxicity and efficacy. Trial design proceeds by treating cohorts of two patients simultaneously receiving different dose combinations and response adaptive randomization. We compare trial safety and efficiency of the estimated maximum tolerated dose (MTD) curve between models that include an interaction term with models without the synergism parameter with extensive simulations. Under a selected class of dose-toxicity models and dose escalation algorithm, we found that not including an interaction term in the model can compromise the safety of the trial and reduce the pointwise reliability of the estimated MTD curve.

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The Likelihood Ratio Test and Full Bayesian Significance Test under small sample sizes for contingency tables

Hypothesis testing in contingency tables is usually based on asymptotic results, thereby restricting its proper use to large samples. To study these tests in small samples, we consider the likelihood ratio test and define an accurate index, the P-value, for the celebrated hypotheses of homogeneity, independence, and Hardy-Weinberg equilibrium. The aim is to understand the use of the asymptotic results of the frequentist Likelihood Ratio Test and the Bayesian FBST -- Full Bayesian Significance Test -- under small-sample scenarios. The proposed exact P-value is used as a benchmark to understand the other indices. We perform analysis in different scenarios, considering different sample sizes and different table dimensions. The exact Fisher test for $2 \times 2$ tables that drastically reduces the sample space is also discussed. The main message of this paper is that all indices have very similar behavior, so the tests based on asymptotic results are very good to be used in any circumstance, even with small sample sizes.

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Comparing probabilistic predictive models applied to football

We propose two Bayesian multinomial-Dirichlet models to predict the final outcome of football (soccer) matches and compare them to three well-known models regarding their predictive power. All the models predicted the full-time results of 1710 matches of the first division of the Brazilian football championship and the comparison used three proper scoring rules, the proportion of errors and a calibration assessment. We also provide a goodness of fit measure. Our results show that multinomial-Dirichlet models are not only competitive with standard approaches, but they are also well calibrated and present reasonable goodness of fit.

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