Table 1.
Recommended minimum standard timepoints for perioperative sample collection
Timepoint | Timeframe | Potential correlative outcomes |
---|---|---|
Treatment naive | Prior to treatment, concurrent with initial clinical staging | Pathological response to neoadjuvant therapy, long-term survival and disease status |
Post-neoadjuvant therapy and/or restaging | ≥4 weeks after completing neoadjuvant therapy; ≤2 weeks of concurrent clinical assessment or restaging and/or resection | Pathological response to neoadjuvant therapy, neoadjuvant rectal score |
Post-resection | 4–8 weeks after surgical resection with a curative intent | Long-term survival and disease status, including overall survival, disease-free survival and recurrence-free survival |
After adjuvant therapy or completion of all potentially curative therapy; minimal residual disease | 2–8 weeks after completion of all curative-intent therapy | |
Disease relapse or recurrence | ≤2 weeks, concurrent with clinical assessment and/or restaging showing evidence of disease relapse and/or recurrence |