Les inscriptions sont à présent ouvertes pour le 23ème colloque scientifique de l'EFSA, organisé conjointement avec le groupe Evidence Based Toxicology Collaboration (EBTC).
D’éminents scientifiques du monde entier participeront à ce colloque pour explorer les orientations futures en matière d’intégration des données probantes dans l'évaluation des risques chimiques pour l’homme. Voici la liste des intervenants principaux :
- Donald Rubin et Stijn Vansteelandt : inférence causale
- Julian Higgins et Sofia Dias : synthèse des preuves, méta-analyse
- Kris Thayer et Holger Schunemann : synthèse des preuves, méthodes GRADE et GRADE-based
- Marc Aerts, Wout Slob, Matthew Wheeler : modélisation dose-réponse
Le colloque aura lieu à Lisbonne, au Portugal, les 25 et 26 octobre prochains. C’est le 23ème colloque scientifique de l'EFSA et il est organisé conjointement avec l’EBTC de la Johns Hopkins Bloomberg School of Public Health.
Ne manquez pas cette occasion unique de participer à un débat passionnant et de façonner l'évolution de l'intégration des preuves en compagnie des meilleurs experts en la matière.
Evidence-based scientific assessments involve applying structured and standardised approaches to minimise bias and maximise impartiality and transparency in the process for collecting, evaluating and combining evidence relevant to well-formulated research questions, according to pre-defined protocols. These approaches are well-established for healthcare intervention questions and their value has been extensively acknowledged also in the field of chemical risk assessment, where their application continues to be explored.
In evidence-based scientific assessments, evidence synthesis is the step that occurs after appraising the validity of the individual studies selected for the assessment. In evaluations of the efficacy of therapeutic interventions, this is usually done through meta-analysis, which encompasses statistical methods for combining data from similar, readily-comparable studies.
In hazard identification and characterisation for chemical risk assessment, the underlying evidence bases are diverse and not readily comparable. Unlike in medicine, in this research field heterogeneity of evidence stems from not only varying degrees of validity and precision of studies and diverse data types (e.g. individual Vs aggregated), but also from dissimilar designs/settings/models, endpoints, routes of exposure, or evidence streams (human observational studies, experimental animal studies, in vitro and computational models data). As such, a process for combining evidence not only within- but also across evidence streams is needed. This process is defined as ‘evidence integration’ and is particularly relevant for assessing effects caused by exposure to a chemical substance (hazard identification), and for deriving health-based guidance values through dose-response modelling (hazard characterisation).
Evidence integration is a recognised challenge in evidence-based risk assessment and to be conducted soundly, it has to draw on valid approaches to collecting and evaluating evidence in prior steps in the risk assessment, and the integration methodology itself needs to be valid. Different methods for integrating evidence exist, ranging from approaches based on expert judgement, through structured qualitative methods, to complex quantitative methods.
Objectives of the Colloquium
EFSA and EBTC have organised a colloquium, guided by experts in the field, with the goal of developing a multi-stakeholder understanding of the best practices for evidence integration in human risk assessment of chemicals, with a specific focus on hazard identification and on combining multiple studies and endpoints for dose-response modelling in hazard characterisation.
We will discuss current practice, challenges, recent developments and innovative approaches to integrating evidence within and across evidence streams and to combining multiple studies and endpoints. Even if the case-studies and examples discussed throughout the colloquium will be specific for the field of chemicals, we aim at addressing these methodological aspects from a broad, cross-cutting perspective, relevant to other research contexts (e.g. dietary reference values).
Relevant EFSA projects
EFSA PROMETHEUS (PROmoting METHods for Evidence Use in Scientific Assessments) project: https://www.efsa.europa.eu/en/methodology/evidence
EFSA (European Food Safety Authority) Scientific Committee, 2016. Guidance on Uncertainty in EFSA Scientific Assessment - Draft version for internal testing. Available at https://www.efsa.europa.eu/en/topics/topic/uncertainty
EFSA (European Food Safety Authority) Scientific Committee, 2017. Guidance on The Use of the Weight of Evidence Approach in Scientific Assessments - Draft version for public consultation. Available at https://www.efsa.europa.eu/sites/default/files/consultation/170306-0.pdf
EFSA (European Food Safety Authority) Scientific Committee, 2017. Guidance on Biological Relevance- Draft version for public consultation. Available at http://www.efsa.europa.eu/sites/default/files/consultation/170306.pdf
Structure of the meeting
Colloquia are not consensus meetings: their objective is to convene leading scientists from Europe and beyond. Rather than offering a series of lectures, this Colloquium will provide ample opportunity for an exchange of expert opinions and scientific debate. Following the opening plenary session with introductory key note speeches, the meeting will be structured to enable participants to reach conclusions and make recommendations in small groups, focusing the discussions on four specific topics.
The four discussion groups (DGs) will focus on the following themes:
- DG 1 – Qualitative methods for integrating evidence within- and across evidence streams for hazard identification
- DG 2 – Bias-adjusted meta-analysis
- DG 3 – Quantitative approaches to combining evidence across evidence streams for hazard identification
- DG 4 – Using multiple endpoints and multiple studies for dose-response modelling: quantitative approaches
The outcome of the discussion groups will be presented and discussed in a final plenary session to formulate conclusions of the Colloquium and, as appropriate, recommendations. The outcomes of the Colloquium will be summarised in an overall report after the meeting.
Dates and Venue
The Colloquium will be held in Lisbon, Portugal. The meeting will start at 08:00 on 25 October 2017 and will end at 13:30 on 26 October 2017. Further details on the venue and logistics will be communicated to participants upon confirmation of selection.
English will be the official language of the Colloquium. No translation will be provided.
The briefing notes included in this page contain references to relevant background documents to inform about the contents of each discussion group.
The presentations and the conclusions of the meeting will be made available on the EFSA website. EFSA will also publish a summary report of the event in the form of a booklet.
For more information on the Scientific Colloquium, please do not hesitate to contact us at scientific.colloquia [at] efsa.europa.eu
Who should attend?
For practical reasons, to allow in-depth discussion, participation is limited to a maximum of 120 experts, including plenary speakers and other experts already identified by EFSA.
Interested experts are requested to register and to indicate their area(s) of expertise (see the registration form) in order to be considered for participation. Participants will be selected to ensure a sufficient representation of the various fields of expertise, as well as a broad geographical balance. The registration form can be found HERE.
Please note that registration may close once the maximum number of participants is reached or at the latest by 31 August
Applicants will then as soon as possible after closure of registration be informed whether they are selected for participation. Selected participants will be asked to make their own travel arrangements at their own expense. Concerning accommodation, EFSA has made a block-booking for the nights of 24 and 25 October 2017. Selected participants will be requested to make their own reservation when participation is confirmed. There is no fee for participation.