
Post-Treatment Surveillance Workshop Highlights
Discussing post-treatment surveillance issues in cancer with a focus on imaging and liquid biopsies. The workshop aims to identify priorities for evaluation in clinical trials, including strategic priorities, trial prioritization, and implementation plans.
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Presentation Transcript
NCI Workshop: Issues in Post-Treatment Surveillance Lalitha K. Shankar, MD, PhD, Cancer Imaging Program, NCI March 26, 2018
NCI Planning Committee Jeff Abrams, Barry Kramer, Paul Jacobsen (DCTD, DCP & DCCPS) Lalitha Shankar, Bhupinder Mann, Carmen Allegra, Shakuntala Malik, Larissa Korde, Nita Seibel, Worta McCaskill-Stevens and Anne Menkens
Conference Goals and Rationale: To discuss issues in post treatment surveillance given the current advances in imaging and liquid biopsies Specific discussions will occur in Breast, Colon, NSCLS, Prostate and Testicular cancer
Meeting Goals/Objectives Identify and prioritize histologies and tools that are most suitable to be evaluated in this setting, in NCTN and NCORP clinical trials Format: 1stmorning: Plenary sessions on Issues in Post-treatment surveillance from various perspectives 1stafternoon: Breakout sessions for the different cancer types 2ndMorning: Reports from breakout sessions and discussion
Meeting Outcomes Anticipated outputs from the meeting - Executive Summary - Strategic priorities for studies most appropriate for study in NCTN and NCORP trials (Phase II and III) - Trial prioritization - Implementation plan - Identification of questions that could be answered by registries
NCI Resources for Early Stage Clinical Evaluation of Diagnostic Tools PAR-18-629: Integration of Imaging and Fluid- Based Tumor Monitoring in Cancer Therapy (R01 Clinical Trial Optional) PAR-18-560: Investigator-Initiated Early Phase Clinical Trials for Cancer Treatment and Diagnosis PAR-18-530: Academic-Industrial Partnerships for Translation of Technologies for Diagnosis and Treatment (R01 - Clinical Trial Optional) PAR-18-317: Assay Validation of High Quality Markers for Clinical Studies in Cancer (UH2/UH3 Clinical Trial Not Allowed)