The Corporate Workshop session will take place on Sunday, October 6 from 12:00 PM - 2:00 PM and offer an opportunity for you to hear about the latest products from the participating companies. There is no charge to attend. The first 100 attendees to arrive by 12:10 PM, will receive a 10 USD Visa gift card, while supplies last.
“Enabling Operational Efficiencies In High-Parameter Leukemia And Lymphoma Subtyping Using Cytek AuroraTM Full Spectrum Flow Cytometers”
David Ng, MD, FCAP
Director of Flow Cytometry and Applied AI
ARUP Laboratories
“BD FACS: 50 Years Enabling Science Through Flow Cytometry”
Rodrigo Pestana, PhD
Sr Scientific Manager
BD Biosciences
Flow cytometry is a versatile technology initially used in clinical sciences to aid in the diagnosis, monitoring, and treatment response of hematological and infectious conditions. Its applications have since expanded to include transplantation and transfusion, identification of immune disorders, and monitoring immune responses. Nowadays, flow cytometry is routinely applied to support the diagnosis and classification of blood cancers and detect minimal/measurable residual disease, to identify and quantify different types of immune cells for various disorders and disease states, as well as for numerous applications from basic to applied sciences, including some involved in drug development and translational research.
Partnership between industry, academy and clinical scientists have shaped and enhanced our understanding of immunology, cell biology, and hemato-oncology through the continuous evolution of flow cytometry. Our talk celebrates 50 years of innovative contributions from BD and scientists in the field of flow cytometry since the introduction of the Fluorescence Activated Cell Sorter (FACS), in 1974. This journey of perpetual innovation includes the development of monoclonal antibodies, fluorochromes, and technologies that transformed flow cytometry from a single-parameter technique into a method that generates high-parameter data for detailed analysis of individual cells using powerful bioinformatics.
"Validation of a High-Sensitivity 10-Color Flow Cytometric Measurable Residual Disease Assay for Multiple Myeloma"
Melissa Ulas MD, PhD
Medical Director Clinical Laboratory, Temple Health Chestnut Hill Hospital
Interim Medical Director Clinical Laboratory, TUH Episcopal Hospital
Assistant Professor, Clinical Pathology and Laboratory Medicine, Lewis Katz School of Medicine, Temple University
Associate Director, Clinical Chemistry and POCT, Pathology and Laboratory Medicine, Temple University Hospital System
Flow cytometric (FC) detection of measurable residual disease (MRD) in multiple myeloma (MM) is predictive of response to therapy. The investigators developed and validated a high-sensitivity single tube 10-color MM MRD assay. The panel included VS38c and CD138 as backbone markers to detect plasma cells and combine surface and cytoplasmic markers into a single tube following bulk lysis. During this session, the primary investigator will share her team's findings in the validation of the MDR assay using the Sysmex XF-1600TM Flow Cytometer for research use only* and the VenturiOne© Flow Cytometry analysis Software.
Overview
1. Explain key steps needed to complete the MRD assay validation.
2. Discuss the benefits of of using the Sysmex XF-1600 and the VenturiOne software to validate flow cytometry assays.
3. Recognize the regulatory considerations needed to effectively validate flow cytometry assays.
*XF-1600 is For Research Use Only. Not for use in diagnostic procedures. RUO instruments must be validated before use in clinical practice.
“Optimized Workflow for Clinical Flow Cytometry Lab”
Alan Dunlop
Royal Marsden Hospital NHS Trust
London, UK
Year on year clinical flow cytometry laboratories see an increase in not only sample numbers but in the complexity of testing required. There is a similar increase in the volume of quality related tasks required to ensure laboratories maintain accreditation.
This increased workload rarely comes with appropriate resource meaning staff are constantly under pressure to do more in the same number of hours. In an attempt to deal with this rising tide of work our laboratory has undertaken a complete overhaul of the way we function, we have implemented new high parameter flow cytometers, fully automated sample preparation for leukaemia and lymphoma diagnostic testing as well as stem cell enumeration. With the implementation of a new laboratory information system, we have become paper free. This along with offline data analysis has allowed us to facilitate effective remote work at times for over 60% of our staff. This transformation of the way we work has allowed us to focus on developing our next generation of Scientists by training then in data analysis, challenging them with research projects and involving them in quality tasks when previously simply delivering our clinical service was a challenge.