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Ayon Mukherjee

Publications and source records attributed to Ayon Mukherjee.

10 recordsLinked to original sources

Efficient Response-Adaptive Randomization for Multi-arm Trials with Prioritized Composite Endpoints

The efficient randomized-adaptive design attains the minimal possible variance of the allocation proportion for any pre-specified target and has been extended from two to several treatment arms, but both versions target a single response. Confirmatory trials increasingly rely on several prioritized endpoints, typically efficacy followed by safety, that cannot be reduced to one summary without losing information. The efficient randomized-adaptive design is extended here to targets driven by the net treatment benefit of generalized pairwise comparisons, allowing any number of arms and endpoints of mixed type, including censored time-to-event outcomes. Strong consistency, a law of the iterated logarithm, and asymptotic normality of the allocation proportions are established by combining a sequential H\'ajek projection for the net benefit with the martingale technique used for the original design, and the design is shown to attain the semiparametric efficiency bound within the class of designs that track a smooth function of the net benefit. In simulations calibrated to a three-arm phase III melanoma trial, the proposed design concentrates allocation on the superior treatment more efficiently than designs driven by a single endpoint, while preserving type I error and power. A redesign of the trial illustrates the practical benefit, and the approach is discussed in relation to current regulatory thinking on adaptive designs for confirmatory trials.

stat.ME

Chiral, parity-doublet, effective-Lagrangian mean-field theories for nuclear and astrophysical phenomenology

Chiral-parity (parity-doublet) effective Lagrangian models provide a compact and symmetry-consistent framework for describing baryons and their negative-parity partners in terms of linearly-realized chiral symmetry. Unlike the conventional, linear, sigma model; the parity-doublet approach accommodates a chirally-invariant mass term, $m_0$, allowing finite baryon-masses even when the chiral condensate melts. This feature enables a unified treatment of hadronic matter across vacuum, nuclear and dense astrophysical regimes. This compact review summarizes the key structures of parity-doublet Lagrangians; outlines the mean-field formulation for nuclear and stellar matter; and highlights recent phenomenological and lattice constraints on the chirally-invariant mass. Emphasis is placed on mirror versus na\"ive chiral assignments; the role of vector interactions in achieving nuclear saturation; and the implications of parity doubling for the equation-of-state of dense matter and neutron-star cooling. The review concludes with current theoretical challenges and perspectives for extending these models beyond the mean-field approximation.

hep-ph

Bayesian Optimal Phase II design with optimised stopping boundaries and response-adaptive randomisation

The Bayesian Optimal Phase II (BOP2) framework is a flexible trial design that can naturally facilitate complex adaptations due to its Bayesian setting. BOP2 uses equal randomisation and equally placed interim analyses in its design, but it is unclear whether these give the best operating characteristics. By incorporating Bayesian Response-Adaptive Randomisation (BRAR) and optimal interim analysis placement, we show that allocation to the best treatment and expected sample size can be improved with minimal impact on power. We discuss recommendations on implementing these adaptations, using simulation-based evidence, to give practical advice to practitioners. Reproducible code for the simulations is freely provided.

stat.AP

Estimands for Randomized Discontinuation Designs in Oncology

Randomized discontinuation design (RDD) is an enrichment strategy commonly used to address limitations of traditional placebo-controlled trials, particularly the ethical concern of prolonged placebo exposure. RDD consists of two phases: an initial open-label phase in which all eligible patients receive the investigational medicinal product (IMP), followed by a double-blind phase in which responders are randomized to continue with the IMP or switch to placebo. This design tests whether the IMP provides benefit beyond the placebo effect. The estimand framework introduced in ICH E9(R1) strengthens the dialogue among clinical research stakeholders by clarifying trial objectives and aligning them with appropriate statistical analyses. However, its application in oncology trials using RDD remains unclear. This manuscript uses the phase III JAVELIN Gastric 100 trial and the phase II trial of sorafenib (BAY 43-9006) as case studies to propose an estimand framework tailored for oncology trials employing RDD in phase III and phase II settings, respectively. We highlight some similarities and differences between RDDs and traditional randomized controlled trials in the context of ICH E9(R1). This approach aims to support more efficient regulatory decision-making.

stat.ME

Estimands for Early Phase Dose Optimization Trials in Oncology

Phase I dose escalation trials in oncology generally aim to find the maximum tolerated dose (MTD). However, with the advent of molecular targeted therapies and antibody drug conjugates, dose limiting toxicities are less frequently observed, giving rise to the concept of optimal biological dose (OBD), which considers both efficacy and toxicity. The Estimand framework presented in the addendum of the ICH E9(R1) guidelines strengthens the dialogue between different stakeholders by bringing in greater clarity in the clinical trial objectives and by providing alignment between the targeted estimand under consideration and the statistical analysis methods. However, there lacks clarity in implementing this framework in early phase dose optimization studies. This manuscript aims at discussing the Estimand framework for dose optimization trials in oncology considering efficacy and toxicity through utility functions. Such trials should include Pharmacokinetics (PK) data, toxicity data, and efficacy data. Based on these data, the analysis methods used to identify the optimized dose/s are also described. Focusing on optimizing the utility function to estimate the OBD, the population-level summary measure should reflect only the properties used for the estimating this utility function. A detailed strategy recommendation for intercurrent events has been provided using a real-life oncology case study. Key recommendations regarding the estimand attributes include that in a seamless Phase I/II dose optimization trial, the treatment attribute should start when the subject receives the first dose. We argue that such a framework brings in additional clarity to dose optimization trial objectives and strengthens the understanding of the drug under consideration that would enable the correct dose to move to Phase II of clinical development.

stat.ME

Multi-particle quantum-statistical correlation functions in a Hubble-expanding hadron gas

Quantum-statistical correlation measurements in high-energy physics represent an important tool to obtain information about the space-time structure of the particle-emitting source. There are several final state effects which may modify the measured femtoscopic correlation functions. One of these may be the interaction of the investigated particles with the expanding hadron gas, consisting of the other final state particles. This may cause the trajectories - and hence the phases - of the quantum-correlated pairs to be modified compared to free streaming. The resulting effect and could be interpreted as an Aharonov-Bohm-like phenomenon, in the sense that the possible paths of a quantum-correlated pair represent a closed loop, with an internally present field caused by the hadron gas. In this paper, the possible role of the effect in heavy-ion experiments is presented with analytical calculations and a simple numerical model. The modification of the strength of multi-particle Bose-Einstein correlation functions is investigated, and the is found that in case of sufficiently large source density, this effect may play a non-negligible role.

hep-ph

Kaon femtoscopy with Lévy-stable sources from $\sqrt{s_{_{\rm NN}}} = 200$ GeV $\mathrm{Au}+\mathrm{Au}$ collisions at RHIC

Femtoscopy has the capacity to probe the space-time geometry of the particle-emitting source in heavy-ion collisions. In particular, femtoscopy of like-sign kaon-pairs may shed light on the origin of non-Gaussianity of the spatial emission probability density. The momentum-correlations between like-sign kaon-pairs are, hence, measured in data recorded by the STAR experiment, from $\sqrt{s_{_{\rm NN}}} = 200$ GeV $\mathrm{Au}+\mathrm{Au}$ collisions at RHIC, BNL. Preliminary results hint at the, possible, existence of non-Gaussian, Lévy-stable sources; and signal the, likely, presence of an anomalous diffusion process; for the identically-charged kaon-pairs so produced. More statistically significant studies, at lower centre-of-mass energies, may contribute to the search for the critical end point of QCD as well.

nucl-ex

Dilepton Signature of a First-Order Phase Transition

The search for a first-order phase transition in strongly interacting matter is one of the major objectives in the exploration of the phase diagram of Quantum Chromodynamics (QCD). In the present work we investigate dilepton radiation from the hot and dense fireballs created in Au-Au collisions at projectile energies of 1-2 $A$GeV for potential signatures of a first-order transition. Toward this end, we employ a hydrodynamic simulation with two different equations of state, with and without a phase transition. The latter is constrained by susceptibilities at vanishing chemical potential from lattice-QCD as well as neutron star properties, while the former is implemented via modification of the mean-fields in the quark phase. We find that the latent heat involved in the first-order transition leads to a substantial increase in the low-mass thermal emission signal, by about a factor of two above the cross-over scenario.

nucl-th

Effects of a non-zero strangeness-chemical potential in strong interaction models

The effect of a non-zero strangeness chemical potential on the strong interaction phase diagram has been studied within the framework of the SU(3) quark-hadron chiral parity-doublet model. Both, the nuclear liquid-gas and the chiral/deconfinement phase transitions are modified. The first-order line in the chiral phase transition is observed to vanish completely, with the entire phase boundary becoming a crossover. These changes in the nature of the phase transitions are expected to modify various susceptibilities, the effects of which might be detectable in particle-number distributions resulting from moderate-temperature and high-density heavy-ion collision experiments.

hep-ph

Nuclear interactions and net-proton number fluctuations in heavy ion collisions at the SIS18 accelerator

The effect of nuclear interactions on measurable net-proton number fluctuations in heavy ion collisions at the SIS18/GSI accelerator is investigated. The state of the art UrQMD model including interaction potentials is employed. It is found that the nuclear forces enhance the baryon number cumulants, as predicted from grand canonical thermodynamical models. The effect however is smeared out for proton number fluctuations due to iso-spin randomization and global baryon number conservation, which decreases the cumulant ratios. For a rapidity acceptance window larger than $Δy> 0.4$ the effects of global baryon number conservation dominate and all cumulant ratios are significantly smaller than 1.

nucl-th