Identifying the optimal post-surgical timing of molecular residual disease (MRD) detection in colorectal cancer (CRC) using an ultra-sensitive assay: Interim results from the VICTORI study.
Abstract
275 Background: While detection of MRD using ctDNA is prognostic for recurrence in CRC, some patients still recur prior to MRD detection. VICTORI is prospectively investigating NeXT Personal, an ultra-sensitive NGS-based MRD assay, to profile patients with resected CRC. Methods: Patients with CRC treated with curative intent (all stages) are tested for MRD using NeXT Personal, a bespoke assay with up to ~1,800 tumor-informed single nucleotide variants (SNVs) identified from whole-genome sequencing. Plasma is collected prior to surgery, every 2 weeks post-surgery up to week 8 (MRD landmark window), and every 3 months for up to 3 years (surveillance). We present preliminary results on 397 samples from the first 62 patients. Results: A total of 62 patients (N=36 rectal [58%], N=26 colon [42%]; N=46 stage I-III [74%], N=16 stage IV [26%]) were included in our analysis. Baseline pre-surgical sensitivity (treatment naive) was 93.5% [N=29/31]. Pre-surgical positivity rate in patients who had received neoadjuvant therapy and had residual cancer at the time of surgery was 67% [N=16/24]. 60 patients were evaluable for clinical outcomes. At a median follow-up of 355 days, 15 patients (25%) had a recurrence. Of these, all patients were ctDNA-positive prior to recurrence (100%, 14/14; 1 pt excluded due to lack of samples prior to recurrence). ctDNA detection preceded clinical relapse by a median of 194 days [range: 5-397]); ctDNA for 78.6% (N=11/14) were first detected in the MRD landmark window. All landmark-positive recurrences occurred within one year of surgery. The 14 recurrent cancers with samples were first detected at a median ctDNA concentration of 28.7 parts per million (PPM) (range 2.4-111,120), with 64.3% (9/14) of those detections in the ultra-low range of <100 PPM. MRD detection at week 4 and week 8 had the greatest reduction in RFS (HR 12.86 [2.74-60.28], p=0.0012 week 4; HR 16.14 [3.52-74.09], p=0.0004 week 8), with weeks 4, 6 and 8 having similar higher prevalence of ctDNA detection (36.0% [18/50], 35.3% [18/51], 38.5% [20/52] respectively). Week 2 detection rate was 17.0% (8/46). cfDNA concentration was highest at week 2 (4.63ng/ml vs. 2.22 at baseline, p=0.00028) and 4 (3.68 vs. 2.22, p=0.0081), returning to baseline levels at week 6 (2.28 vs. 2.22, p=0.67) and 8 (2.48 vs. 2.22, p=0.64). Conclusions: In this interim report after a median ~1 year follow-up, NeXT Personal detected MRD for all patients prior to disease recurrence. Most initial MRD detection was in the ultra-sensitive range <100ppm and detection at 4-8 weeks after surgery was highly prognostic for recurrence.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Joao Paulo Solar Vasconcelos
BC Cancer - Vancouver, University of British Columbia, Vancouver, BC, Canada
Emma Titmuss
BC Cancer - Vancouver, Vancouver, BC, Canada
Fabio Navarro
Personalis, Inc., Menlo Park, CA
Charles Abbott
Personalis, Inc., Fremont, CA
Brendan Chia
BC Cancer - Vancouver, Vancouver Cancer Centre, Vancouver, BC, Canada
James T Topham
Pancreas Centre BC, Vancouver, BC, Canada
Gale Ladua
BC Cancer - Vancouver, Vancouver Cancer Centre, Vancouver, BC, Canada
Tharani Krishnan
Flinders Medical Centre, Bedford Park, Australia
Daniela Hegebarth
BC Cancer - Vancouver Cancer Centre, Vancouver, BC, Canada
Howard J Lim
BC Cancer - Vancouver, University of British Columbia, Vancouver, BC, Canada
Karamjit Gill
BC Cancer - Vancouver, Vancouver, BC, Canada
Sharlene Gill
BC Cancer–Vancouver, Vancouver, BC, Canada
Carl J. Brown
Providence Health - St. Paul's Hospital, Vancouver, BC, Canada
Amandeep (Anu) Ghuman
Providence Health - St. Paul’s Hospital, Vancouver, BC, Canada
Adam Meneghetti
Vancouver General Hospital, Vancouver, BC, Canada
Daniel John Renouf
David F. Schaeffer
Richard Chen
Unibersity of Michigan, Ann Arbor, Michigan, United States
Sean Michael Boyle
Personalis, Inc., Fremont, CA
Jonathan M. Loree