The Precision Oncology: Genomics Guided Care Webinar Series recordings and slides are available to all ESMO account holders.
Precision Oncology: Genomics Guided Care – How to Prepare and Read Genomics Reports for Clinical Practice?
Chair's welcome
It is with great pleasure that I invite you to participate in the webinar dedicated to how to prepare and read genomics report for clinical practice. This webinar is a part of four complimentary ESMO webinars in a series focusing on genomics guided cancer care.
I am delighted to announce the presentations by distinguished experts who will join me in this webinar. We will begin with providing key considerations for structure of genomics report. This will follow with discussion around functional and clinical annotation of next-generation sequencing (NGS) data for cancer patient management, as well as reporting and management of incidental findings in tumour NGS.
Overall, the programme is designed to increase knowledge in how to read and interpret a clinically oriented genomics reports, how to interpret functional impact and clinical relevance classification systems for mutations in genomics reports and to discuss indications of secondary germline testing based on reports from tumour-only genomics tests. It is designed for those oncologists keen to keep abreast with rapidly evolving molecular oncology approaches and their applications into clinical practice.
The webinar will conclude with a live discussion of questions submitted by the audience whilst the webinar is taking place.
I encourage you to register and join us all in this new ESMO activity.
Dr. Joaquin Mateo
Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
Speakers
Joaquin Mateo
Chair
Joris Van De Haar
Debyani Chakravarty
Clare Turnbull
Programme
Time |
Title |
Speaker |
|---|---|---|
5 min |
Welcome and Introduction |
Joaquin Mateo |
10 min |
Structure of Genomics Reports |
Joris van der Haar |
10 min |
Functional and Clinical Annotation of NGS Data for Cancer Patient Management |
Debyani Chakravarty |
10 min |
Reporting and Management of Germline Findings in Tumour NGS |
Clare Turnbull |
20 min |
LIVE Q & A |
All |
5 min |
Conclusions |
Joaquin Mateo |
Live viewers of the webinar will be awarded a certificate of attendance and 1 ESMO-MORA category 1 point
Learning objectives:
- Increase knowledge in how to read and interpret clinically oriented genomics reports.
- Learn how to interpret “functional impact" and "clinical relevance" of classification systems for mutations in genomics reports.
- Discuss indications of secondary germline testing based on reports from tumour-only genomics tests.
Supported by
Meeting resources
The Precision Oncology: Genomics Guided Care Webinar Series recordings and slides are available to all ESMO account holders.