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DAY 1, May 22, 2023 (10:00 am to 2:00 pm EDT) 

Welcome and Opening Comments

Keyvan Farahani, PhD, Center for Biomedical Informatics and Information Technology, National Cancer Institute, National Institutes of Health

Session 1: Report of the MIDI Task Group

Report of the Medical Image De-Identification (MIDI) Task Group - Best Practices and Recommendations

Session Chair: David Clunie, MBBS, PixelMed, Inc.

In this session, David Clunie, chair of the MIDI Task Group, will summarize the best practices and recommendations included in the task group's report, recently available in pre-print, followed by a question and answer period.

Session 2: Tools for Conventional Approaches to De-Identification

Session Chair: Fred Prior, PhD, University of Arkansas for Medical Sciences

In this session, speakers will share methods currently in use for medical de-identification.

Session 3: International Approaches to De-Identification

Session chair: Dana Pe’er, Memorial Sloan Kettering

This session will focus on multimodal learning in data limited contexts, including cell-cell interactions and predicting outcomes. Dealing with imbalances across multimodal data sets and foundational models will also be discussed.

Speakers:

Elena Fertig, Johns Hopkins
Elham Azizi, Columbia
Livnat Jerby, Stanford

Panelists:

Marianna Rapsomaniki, IBM Research
Arjun Krishnan, University of Colorado
 
DAY 2, April 4, 2023 (11 am to 3:30 pm EDT) 

Session 4: Making use of large-scale, structured clinical research data and image repositories

Session chair: Ziad Obermeyer, UC Berkeley

In this session, researchers will discuss the use of large-scale clinical research data for machine learning models. Discussion topics include the use of synthetic data, considerations of bias, generalizable models, and development of digital twins.

Speakers:

Chris Probert, InSitro
James Zou, Stanford
Mihaela van der Schaar, University of Cambridge

Panelists:

Lily Peng, Verily
Matthew Lungren, Microsoft/UCSF



Session 5: Improving modeling of real-world evidence data in clinical research and clinical trial design

Session chair: Tianxi Cai, Harvard

This session will focus on real-world evidence (RWE) data modeling, including issues associated with RWE data such as electronic health record coding and unbalanced data, towards the development of clinical trials.

Speakers:

Sean Khozin, MIT
Limor Appelbaum, Beth Israel Deaconess
Ryan Copping, Genentech

Panelists:

Donna Rivera, FDA
Khaled El Emam, University of Ottawa



Session 6: Cross-cutting discussion with session chairs

Session chair: Olivier Gevaert, Stanford University

Discussion of the approaches and challenges identified during the workshop and opportunities for the future.

Panelists:

Caroline Uhler, MIT and Broad Institute
Trey Ideker, UCSD
Dana Pe’er, Memorial Sloan Kettering
Ziad Obermeyer, UC Berkeley
Tianxi Cai, Harvard