Agenda
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TO VIEW THE MEETING RECORDING, please visit the links below:
Workshop Day 1 (December 10, 2020)
Workshop Day 2 (December 11, 2020)
December 10th, 2020 |
|
9:00am – 9:15am EST |
NCI Welcome |
9:15am – 11:45pm EST |
Choosing the Target: Specificity and Toxicity 9:15am – 9:45am, Selecting and Validating Targets, Isolating High Affinity TCRs, and Engineering T Cells That Can Be Effective in Therapy, Philip Greenberg, MD (Fred Hutchinson Cancer Research Center) 9:45am – 10:15am, Development of Combinatorial Antigen Sensing T Cell Therapeutics for Solid Tumors, Kole Roybal, PhD (University of California, San Francisco) 10:15am – 10:45am, Targeting Solid Malignancies With “Public” Neoantigen-Specific T Cell Receptors, Christopher Klebanoff, MD (Memorial Sloan Kettering Cancer Center) 10:45am – 11:15am, Safety and Clinical Activity of Engineered TCR-T Cells for HPV-Associated Cancers, Christian Hinrichs, MD (National Cancer Institute) Panel Discussion |
11:45am – 12:30pm EST |
Keynote Talk Approaches to Augment Potency of CAR T Cell Therapies, Crystal Mackall, MD (Stanford University) |
12:30pm – 1:00pm EST |
Break |
1:00pm – 3:30pm EST |
Reaching the Target: Modulating the Tumor Microenvironment 1:00pm – 1:30pm, Feast to Famine: Preparing Therapeutic T Cells for Intratumoral Function Through Metabolic Reprogramming, Greg Delgoffe, PhD (University of Pittsburgh) 1:30pm – 2:00pm, Armored CAR T Cells and Solid Tumor Malignancies, Renier Brentjens, MD, PhD (Memorial Sloan Kettering Cancer Center) 2:00pm – 2:30pm, Enhancing Cell Therapies by Overcoming TGFβ in the TME, Catherine Bollard, MD, MBChB (Children’s National Research Institute and George Washington University) 2:30pm – 3:00pm, Does It Make Sense to Add Immune Checkpoint Blockade to Adoptive Cell Transfer Therapies? Antoni Ribas, MD, PhD (University of California, Los Angeles) Panel Discussion |
3:30pm – 4:00pm EST |
Break |
4:00pm – 6:30pm EST |
Immune Cell Fitness and Persistence 4:00pm – 4:30pm, The Tug-o-War Between CAR T and Solid Tumors, Carl June, MD (University of Pennsylvania) 4:30pm – 5:00pm, Driving CAR T Cells into Solid Tumors Without Exhaust(ion), Stanley Riddell, MD (Fred Hutchinson Cancer Research Center) 5:00pm – 5:30pm, Decoding T Cell Dysfunction in Solid Tumors, Andrea Schietinger, PhD (Memorial Sloan Kettering Cancer Center) 5:30pm – 6:00pm, Decoding and Reprogramming T Cell Fitness with CRISPR, Alex Marson, MD, PhD (University of California, San Francisco) Panel Discussion |
December 11th, 2020 |
|
8:45am – 9:00am EST |
Day 1 Recap |
9:00am – 9:45am EST |
Keynote Talk |
9:45am – 12:15pm EST |
Alternative Approaches: Looking Beyond Traditional CAR-T Cells 9:45am – 10:15am, Cellular Therapy of Solid Epithelial Cancers Using Naturally Occurring or Genetically Modified Anti-Tumor T Cells, Steven Rosenberg, MD, PhD (National Cancer Institute) 10:15am – 10:45am, Looking Beyond Traditional CAR-T Cells: Unconventional T Cells, Stem Cell Engineering, and an Off-The-Shelf Cell Therapy, Lili Yang, PhD (University of California, Los Angeles) 10:45am – 11:15am, Dendritic Cells: Vaccines, Modulation of Tumor Microenvironment and Adoptive T Cell Therapies, Pawel Kalinski, MD, PhD (Roswell Park Comprehensive Cancer Center) 11:15am – 11:45am, Clinical and Immunologic Effects of Bispecific Antibody Targeted T Cells for Metastatic Breast and Pancreatic Cancer, Lawrence Lum, MD, DSC (University of Virginia) Panel Discussion |
12:15pm – 1:00pm EST |
Break |
1:00pm – 3:30pm EST |
Cell Product Manufacturing and Characterization 1:00pm – 1:30pm, The Role of Standards in Supporting Cell-Based Therapies & Genome Editing Technology, Samantha Maragh, PhD (National Institute of Standards and Technology) 1:30pm – 2:00pm, Design, Engineer, Validate, Build, Test: Manufacturing the Next Generation of Cell Therapies Targeting Solid Cancers, Bruce Levine, PhD (University of Pennsylvania) 2:00pm – 2:30pm, Manufacturing Matters: Population, Phenotype & Potency, Christine Brown, PhD (City of Hope) 2:30pm – 3:00pm, Considerations for Manufacturing an Allogeneic Cell Product, Barbra Sasu, PhD (Allogene Therapeutics) Panel Discussion |
3:30pm – 4:00pm EST |
Break |
4:00pm – 6:00pm EST |
Cell Therapies: The FDA Perspective 4:00pm – 4:30pm, Regulatory Perspective on the Preclinical Development of Cell-Based Immunotherapies, Alyssa Galaro, PhD (Food and Drug Administration) 4:30pm – 5:00pm, Identification and Assessment of Critical Quality Attributes for Cell-Based Therapies, Irina Tiper, PhD (Food and Drug Administration) 5:00pm – 5:30pm, FDA Clinical Assessment for First-In-Human Studies of Cell Therapy in Solid Tumors, Yuxia Jia, MD, PhD (Food and Drug Administration) Panel Discussion |
6:00pm – 6:15pm EST |
Closing Remarks |