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The Application of RECIST and IrRC in Oncology Clinical Trials

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ON-DEMAND WEBINAR · 2018
The Application of RECIST and IrRC in Oncology Clinical Trials
  • Session Overview: Oncology clinical trial endpoints such as progression free survival (PFS), objective response rate (ORR) and clinical benefit rate (CBR) require accurate disease assessments over time.
WATCH ON DEMAND
Overview
Oncology clinical trial endpoints such as progression free survival (PFS), objective response rate (ORR) and clinical benefit rate (CBR) require accurate disease assessments over time. This webinar will discuss two of the most commonly used disease assessment criteria Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) and Immune-Related Response Criteria (IrRC). First, an overview of RECIST 1.1 and IrRC will be presented. Then the detailed criteria for each assessment method will be discussed with multiple examples of lesion measurements to support the use of each method.
What You'll Learn
  • The ability to categorize baseline tumor lesions for RECIST 1.1 and IrRC.
  • Calculation of the tumor assessments in RECIST 1.1 and IrRC.
  • Determination of objective tumor response in RECIST 1.1 and IrRC including new lesions.
  • Overall response and confirmation in RECIST 1.1 and IrRC and other special notes.
  • The use of RECIST 1.1 and IrRC objective tumor response in time to event analysis.
Meet the Speaker
Tim Breen
Tim Breen’s educational background is a Ph.D. in Physiology and M.S. Bioinformatics. He has more than eighteen years’ experience in clinical data management and eleven years of experience in oncology clinical data management. He is currently the Director of Clinical Research Informatics at the Hoosier Cancer Research Network. Prior to coming to the Hoosier Cancer Research Network, he was a Biostatistics Project Coordinator for the Indiana University, Division of Biostatistics. He is a Certified Clinical Data Manager and a Co-Chair of the SCDM Education Committee.
Earn CEUs
SCDM is authorized by IACET to offer 0.2 CEUs for this education program. Participants are eligible to receive CEUs upon successful completion of the digital assessment questionnaire linked to this session, within 30 days after the purchase of the conference session.

Price
SCDM members: $50
Non-members: $175

Not yet an SCDM member? Purchase this conference session and get a one-year membership with SCDM on us to enjoy all our educational programs and sessions at a discounted price.
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