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Qiqi Deng

Publications and source records attributed to Qiqi Deng.

6 recordsLinked to original sources

Optimal and Efficient Sample Size Re-estimation: A Dynamic Cost Framework

Adaptive sample size re-estimation (SSR) is a well-established strategy for improving the efficiency and flexibility of clinical trials. Its central challenge is determining whether, and by how much, to increase the sample size at an interim analysis. This decision requires a rational framework for balancing the potential gain in statistical power against the risk and cost of further investment. Prevailing optimization approaches, such as the Jennison and Turnbull (JT) method, address this by maximizing power for a fixed cost per additional participant. While statistically efficient, this paradigm assumes the cost of enrolling another patient is constant, regardless of whether the interim evidence is promising or weak. This can lead to impractical recommendations and inefficient resource allocation, particularly in weak-signal scenarios. We reframe SSR as a decision problem under dynamic costs, where the effective cost of additional enrollment reflects the interim strength of evidence. Within this framework, we derive two novel rules: (i) a likelihood-ratio based rule, shown to be Pareto optimal in achieving smaller average sample size under the null without loss of power under the alternative; and (ii) a return-on-investment (ROI) rule that directly incorporates economic considerations by linking SSR decisions to expected net benefit. To unify existing methods, we further establish a representation theorem demonstrating that a broad class of SSR rules can be expressed through implicit dynamic cost functions, providing a common analytical foundation for their comparison. Simulation studies calibrated to Phase III trial settings confirm that dynamic-cost approaches improve resource allocation relative to fixed-cost methods.

stat.ME

A Bayesian model-free dose-finding approach in Phase II clinical trials with the flexibility of historical borrowing

Accurate dose selection in Phase II trials is critical to the success of subsequent Phase III trials, but suboptimal choices remain a leading cause of trial failure and regulatory rejection. Although MCP-Mod is widely adopted and endorsed by regulatory agencies, it requires prespecification of candidate models and is highly sensitive to model misspecification. To address these challenges, we introduce MAP-curvature, a general model-free framework for dose-response modelling that penalises the total curvature of the dose-response curve through a prior. Within this framework, LiMAP-curvature arises as the linear special case, whereas SEMAP-curvature, the focus of this work, employs the sigmoid Emax model, providing greater flexibility to capture nonlinear pharmacological patterns. Through extensive simulations, we show that SEMAP-curvature generally outperforms LiMAP-curvature and MCP-Mod in detecting the dose-response signal, estimating the dose-response curve and identifying the minimum effective dose, with particularly significant improvements under concave downward shapes resembling the sigmoid Emax model. Although SEMAP-curvature exhibits slightly greater variability, it remains robust in accuracy and reliability. We further extend MAP-curvature by integrating it with the Bayesian hierarchical model to enable flexible borrowing of historical data, which improves power and precision, particularly when dose levels overlap across studies. These results highlight MAP-curvature, and in particular SEMAP-curvature with historical borrowing, as a robust and efficient framework for dose selection in early-phase clinical trials.

stat.ME

The Modified Combo i3+3 Design for Novel-Novel Combination Dose-Finding Trials in Oncology

We consider a modified Ci3+3 (MCi3+3) design for dual-agent dose-finding trials in which both agents are tested on multiple doses. This usually happens when the agents are novel therapies. The MCi3+3 design offers a two-stage or three-stage version, depending on the practical need. The first stage begins with single-agent dose escalation, the second stage launches a model-free combination dose finding for both agents, and optionally, the third stage follows with a model-based design. MCi3+3 aims to maintain a relatively simple framework to facilitate practical application, while also address challenges that are unique to novel-novel combination dose finding. Through simulations, we demonstrate that the MCi3+3 design adeptly manages various toxicity scenarios. It exhibits operational characteristics on par with other combination designs, while offering an enhanced safety profile. The design is motivated and tested for a real-life clinical trial.

stat.AP

Frequency tuning of a squeezed vacuum state using interferometric enhanced Bragg diffraction effect

We experimentally demonstrate the optical frequency tuning of a squeezed vacuum state generated from an optical parametric oscillator by using an acousto-optic modulator based bi-frequency interferometer. The systematic efficiency of the frequency tuning device is $91\%$, which is only confined by the optical transmission efficiency of the acousto-optic modulators. The amount of frequency tuning is 80 MHz, which is orders of magnitude larger than the line-width of the laser used to generate the squeezed state, and can in principle be further extended to GHz range. Our investigation shows the interferometric enhanced Bragg diffraction effect can be applied to a variety of other quantum optical states as well, and will serve as a handy tool for quantum network.

quant-ph

An acousto-optic modulator based bi-frequency interferometer for quantum technology

We demonstrate a high performance AOM based bi-frequency interferometer, which can realize either beating or beating free interference for single photon level quantum state. Visibility and optical efficiency of the interferometer are (99.5 +- 0.2)% and (95 +- 1)%, respectively. The phase of the interferometer is actively stabilized by using dithering phase locking scheme, where the phase dithering is realized by directly driving the AOMs with specially designed electronic signal. We further demonstrate applications of the interferometer in quantum technology, including bi-frequency coherent combination, frequency tuning and optical switching. These result show the interferometer is a versatile device for multiple quantum technologies.

quant-ph

Commentary: analyzing binary data using MCPMod when zero counts are expected

Bretz et al (2005) proposed multiple Comparison Procedure and Modeling (MCPMod) method to design and analyze dose-finding study. Pinheiro (2014) then generalized it to various types of endpoint, including but not limited to binary endpoint, survival endpoint, count data, and longitudinal data. Pinheiro (2013) recommended to use the estimated covariance matrix from the observed data to recalculate the optimal contrast and the critical value of the test For many phase II studies it is common to have small sample sizes per arm with low placebo response rates jointly. Under such circumstances, it cannot be excluded to have a zero count observed. For example, when the placebo response rate is 10%, there is about 4% chance to observe zero responders in the placebo group, or other dose group(s), which has a similar response rate as placebo. In this manuscript, we would like to illustrate the potential problem of Pinheiro (2013) using a case study and simulations. An alternative method using Firth's logistic regression was evaluated to get a stable estimate of response for each dose group. In addition, we evaluated two options to address the issue with problematic contrast coefficients.

stat.ME