Our Theses
Methodological aspects of therapeutic studies in rare cutaneous vascular diseases
Today, therapeutic evaluation primarily relies on the randomized controlled trial with a two-parallel group design. However, for rare diseases, this standard is challenging due to the required sample sizes. Thus, this thesis set three objectives, corresponding to three distinct studies. The first objective was to review the study designs used to evaluate therapies in a given group of rare diseases, specifically rare superficial vascular anomalies (SVA), which particularly affect the pediatric population. A systematic literature review analyzing trials conducted between January 2000 and January 2021 on the treatment of rare SVA was carried out. This review helped to compile an inventory of the study designs used as well as the justifications underlying the choice of these methodological designs. The second objective aimed to deepen the analysis of a methodological design identified for the therapeutic evaluation of rare SVA, namely the "individual stepped-wedge randomized trial," in order to facilitate its implementation by determining an appropriate sample size calculation. The validity of this sample size calculation formula has then been assessed using a Monte Carlo simulation approach. Finally, the third objective of the thesis was to identify the methodological design considered most relevant by a panel of experts, to conduct clinical trials on rare SVA. This work used the international Delphi consensus method, bringing together medical experts and patient association representatives, by presenting them with various clinical and therapeutic situations. This approach led to a consensus on several specific clinical situations, thus providing a basis to guide future therapeutic studies in rare SVA.
Randomization of nursing homes and risk of attrition: choice of design and analysis strategy
In a cluster randomized trial, randomization units are groups of individuals, rather than individuals themselves. Nursing homes are facilities for older adults in need of care. Regarding the type of intervention assessed in such settings, cluster randomized trial is as a well-adapted design. With the global ageing of the population, trials in nursing homes are required but still underrepresented and the reasons are, among others, methodological issues such as the high risk of attrition, essentially due to death. The objective of this PhD thesis was to provide a validated approach to estimate an intervention effect when a cluster randomized trial is planned in nursing homes and faces the risk of a high rate of discontinuation due to death. In the first part of this work we investigated, through a methodological review, the strategies used to deal with that attrition. The review was based on reports of cluster randomized trials planned in nursing homes and published between 2005 and 2020 in selected general medicine and geriatric journals with high impact factors. In the second part of this work, we focused on the closed-cohort recruitment strategy, the most frequently used design but also the most exposed to the risk of attrition. The aim of the second part was to assess how an open-cohort design could have been considered as a relevant alternative to a closed-cohort design. The last part of this work was to assess through a Monte Carlo simulation study how bias can be reduced when estimating an intervention effect using an open-cohort design as compared to a closed cohort, in the context of cluster randomized trial in nursing home with not at random missing data.
Most of the interventions assessed in nursing homes are at cluster level, making the open-cohort a well-adapted design. Individual attrition is no longer an issue and it provides low biased estimates of the intervention effect. Open-cohort must be considered more often when cluster randomized trials are planned in nursing homes.
Personal recovery in bipolar disorder: concept definition and measurement tools. Therapeutic patient education as a lever for recovery.
Discover older theses
Methodological and statistical aspects of within-person randomized trials evaluating a topical treatment in dermatology
To assess a topical treatment in dermatology, we may use a within-person (also called split-body) design. Randomization units are no longer patients but rather lesions or body sites. Experimental and control treatments are then applied simultaneously on the different lesions. This study design reduces the inter-observation variability, and therefore the number of patients to be included in the trial. However, this study design presents methodological constraints, notably a risk of intergroup contamination, named the “carry across effect”. The objective of this PhD thesis was to study the methodological and statistical aspects of within-person randomized clinical trials. The first part of this work presents a synthesis of the methodological aspects to be considered when using this design. This work was conducted by a group associating dermatologists and biostatisticians. In the second part, we performed a methodological review of within-person randomized trials published between 2017 and 2021. The methodological aspects identified in the first work were assessed and discussed in this review. The third work focused on the statistical analysis. Using a Monte-Carlo simulation study, we compared the statistical properties of several analysis methods (mixed models and generalized estimating equations). Finally, as an illustration, the last part presents a within-person randomized trial protocol for evaluating topical sirolimus in superficial lymphatic malformations. The within-person design has multiple methodological and statistical specificities that must be taken into account when planning and analyzing the study. Dermatologists and methodologists must also consider patient acceptability.
Characterization of social cognition abilities in behavioral addictions through the prism of gaming and gambling disorders
This thesis focused on social cognition (SC) in the two behavioral addictions (BA) included in international classifications: gaming (GmD) and gambling (GbD) disorders. Two systematic reviews exposed the scarcity of studies linking SC and BA. Nevertheless, studies included in the reviews suggested the presence of an alteration of some of the SC’s components. Additionally, patient-reported outcomes confirmed the presence of interpersonal difficulties. These elements demonstrated the necessity to explore the SC abilities of patients with Gmd or GbD, in order to improve knowledge on addictive processes and propose alternative treatments focused on these difficulties. This thesis presented three studies on gamblers or gamers, whether or not they have an addiction. The first study showed specific allocation of attention toward social information in poker players compared to controls. The second study demonstrated a link between difficulties in identifying facial emotion and GbD and specificities in social metacognition in GmD. Finally, preliminary results of a study regarding GbD patients at the beginning of their treatment showed the importance of taking into account patient-reported outcomes in SC. Those results were discussed in light of clinical et scientific aspects, and put in perspective with future possible research.
Causal inference from observational data: development and applications for critical care
The increasing amount of observational data, especially in critical care, leads to the consideration of causal inference statistical methods. This thesis presents two works that highlight the current challenges of these statistical methods used on observational health data. The first analysis evaluates the impact of barbiturates in a population of trauma brain injured patients prospectively included in the open critical care cohort AtlanRéa. The evaluation of the impact of barbiturates was possible by respecting the assumptions of causal inference and by using a method based on propensity scores: inverse probability weighting.
Beyond the results of this analysis, which showed an increase in mortality in the group treated with barbiturates, we were faced with the problem of the violation of the positivity assumption. We then compared different statistical methods of causal inference in a context of violation of the positivity assumption, which can be associated with an extrapolation issue. The methods predicting the occurrence of the outcome are the most robust in these situations. In this context of accumulation of health data, a perspective of optimization of the use of statistical methods in the framework of causal inference will reside in the use of machine learning algorithms to avoid the problems of model specification.
Multilevel joint modelling of target lesions dynamics and survival : application to the prediction of the response to immunotherapy in bladder cancer
Treatment evaluation in oncology relies on time-to-death and longitudinal measurements of the Sum of Longest Diameters (SLD) of target lesions. Both processes and their association can be analyzed together using a nonlinear joint model. However, using a composite marker such as SLD neglects the heterogeneity in lesion dynamics, which might be exacerbated under immunotherapy.
The main objective of this PhD was to develop multilevel nonlinear joint models of tumor dynamics and their impact on survival, to better characterize all the source of variability in the response to treatment. We relied on data from a phase 2 (IMvigor210) and a phase 3 (IMvigor211) clinical trials of 300 and 900 advanced or metastatic Urothelial Carcinoma (UC) patients, treated with atezolizumab immune checkpoint inhibitor. In a first nonlinear joint model, we showed the impact of tumor location on its dynamics and association with survival. In particular, the liver lesions dynamics was strongly associated with the risk of death as compared to other location. Then, we showed the ability of HMC Bayesian algorithm implemented in Stan software to provide unbiased and precise estimation of the parameters of a nonlinear joint model of SLD and survival, with reasonable sensitivity to prior information. Finally, we developed a Bayesian hierarchical joint model of individual lesions and survival. An additional level of random effect was integrated, specific to the lesion, to quantify the inter-lesions variability under immunotherapy. Using individual dynamic prediction approaches, we showed the benefit of the individual lesions follow-up to identify most at risk patient as compared to SLD follow-up.
This work paves the way for a better understanding of the inter and intra-patient variability in response to new immunotherapy treatments.
Management of complex patients in Pediatric Odontology: Benefit / Risk of practices and improvement pathways, focus on EMONO
The widespread use of MEOPA in dental practices is relatively recent. A review of practices and the legal framework related to the use of nitrous oxide in pediatric odontology seems so particularly relevant. In addition, the emergence of derived uses, outside the context of care or during, leads to increased vigilance towards it. It therefore seems appropriate to identify the effects felt and sought by children during inhalation of MEOPA in the context of dental care. During this thesis, we recalled the context of French use of nitrous oxide and then analyzed it against the benefit / risk of the various other sedations used in pediatric odontology. We then developed a presentation of the different works carried out, their materials and methods and their results. The whole was then discussed and future prospects considered
Expression the cluster effect for binary outcomes
In cluster randomized trials, it is recommended to report a measure of intracluster correlation, such as the intraclass correlation coefficient (ICC), for each primary outcome.
Providing intracluster correlation estimates, which we can also call clustering estimates, may help in sample size calculation of future cluster randomized trials but also in interpreting the results of a trial. For instance, a lower intracluster correlation in the intervention arm as compared to the control one may reveal a better standardization in practices among clusters of the intervention arm, leading to a lower between-cluster heterogeneity in outcomes. Yet, when the outcome is binary, the ICC is known to be associated with the prevalence of the outcome. This may raise issues when using ICC estimates to plan a new study, because expected outcome prevalences may di er from those observed in the study from which the ICC estimates were derived. This association also challenges the interpretation of the ICC because ICC values no longer just depend on clustering level. The aim of this PhD thesis was to study several intracluster correlation measures to identify whether they depend on the outcome prevalence as the ICC does or not. We first focused on the R coefficient, a coefficient initially proposed by Rosner for ophthalmologic data and later extended by Crespi et al. who asserted that the R coefficient may be less influenced by the outcome prevalence than is the ICC. We showed by a simulation study that this assertion is false and that the R coefficient is probably even worse than the ICC as an intracluster correlation measure. We further studied other measures such as the variance partition coefficient, the median odds ratio or the tetrachoric correlation coefficient. We also proposed to consider the relative deviation of an ICC estimate to its theoretical maximum possible value. All these measures were studied in an extensive simulation study, whose conclusion was that all of them depend in some way on the outcome prevalence. Although some measures may be preferred in some situations, none outperforms the others in every situation, and none can be considered independent from the outcome prevalence. Assessing intracluster correlation independently from the outcome prevalence remains an open eld of research.