Purchase the recording of a web seminar you have attended in the past and SAVE 50%! Contact Barnett Customer Service for details: +1 781.972.5400 or toll-free in the U.S. at 800.856.2556.
Web Seminar Archives are available in either USB Flash Drive or DVD Format.
Archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.
Archive: RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials
RECIST stands for Response Evaluation Criteria in Solid Tumors. The National Cancer Institute is the best resource for information, and defines RECIST criteria as “a voluntary, international standard, and not an NCI standard. They are based on a simplification of former methods (WHO, ECOG) and based on measurable disease, i.e., the presence of at least one measurable lesion.” RECIST criteria provide a way to standardize measurement of solid tumors worldwide for any clinical trials that include this data to define study endpoints.
RECIST defines and standardizes how and when subjects are seen to progress, respond or remain stable in terms of their metastatic disease burden during a course of therapy. When these criteria are not well understood at the site level or consistently followed during a trial, it can put the study endpoint data in jeopardy.
- Differentiate between RECIST 1.0 and 1.1
- Describe the components of RECIST/tumor data
- Apply how to correctly calculate disease response
- Identify and predict common trends with tumor data
- Use working knowledge of common trends to help develop Case Report Forms for oncology trials
Who Should Attend
- Clinical Research Coordinators
- Clinical Research Associates
- Clinical Team Managers
- Primary Investigators who are interested in participating in oncology clinical trials, but who do not specialize in oncology or radiology
Vanessa Laroche, B.S., CIP, CQA, C.C.R.P.
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.