Abstract 3845: Enhancing MRD detection through an ultrasensitive ctDNA test: Insights from real-world clinical data

Abstract There is a need for more sensitive circulating tumor DNA (ctDNA) tests that can achieve earlier detection of disease. The NeXT Personal Dx (NPDx) ctDNA MRD test utilizes a bespoke panel of up to ∼1800 variants to achieve ultrasensitive detection down to ∼1 part per million (PPM) of ctDNA with high analytical specificity (>99.9%). Here, we describe the real world performance from more than 5,000 patients profiled using NPDx. In this analysis we examined performance in a variety of real world testing situations and in the ultrasensitive range below 100PPM and 10 PPM, the latter of which has not been previously characterized. Overall, the median limit of detection (LOD) across all timepoints was 1.90 PPM (IQR:1.53-2.70 PPM) across 15 different cancer types. This performance was achieved with a relatively low median cell free DNA (cfDNA) input of 12ng (range 2-30 ng). 45.3% of tests were ctDNA positive overall. The NPDx tests performed well with challenging FFPE tumor samples (low tumor DIN <=3.4 or tumor fraction <=20%), achieving low LODs (median = 2.38 and 2.33 PPM, respectively). NPDx also achieved a median LOD of 3.78 PPM on low TMB tumors (<=0.98 mutation/MB). With ultra-low cfDNA inputs (<=5ng, 11.98% of cohort), NPDx achieved a median LOD of 2.31 PPM. Next we looked at performance in the ultrasensitive ranges below 100 PPM and 10 PPM. 40.2% of detections were in the ultrasensitive range below 100 PPM. Notably, 36.6% of all ultrasensitive detections were found to be <10 PPM (14.7% of detections overall), which aligned well with data from published NeXT Personal clinical studies (Lung - 42.5% in RWD, 40.5% in Black et. al 2025; Breast - 37.5% in RWD, 42.2% in Garcia-Murrillas et. al 2025). Detection rates <10 PPM were consistent across cfDNA input amounts down to 2 ng. For those patients who had sustained ctDNA positivity after a ctDNA negative timepoint, 49% had their first MRD+ detection <10 PPM. Two case studies demonstrate the clinical value of detections below 10 PPM in patient management. A 68-year-old female with squamous NSCLC underwent left upper lobectomy and MRD monitoring with NPDx. After three negative results, two low-level positives (6.2 and 9 PPM) prompted PET imaging that revealed a surgical-site recurrence. ctDNA rose to 80 PPM on the day of imaging, and radiation therapy led to ctDNA clearance. A 67-year-old female with colorectal cancer treated with FOLFOX + Avastin achieved ctDNA clearance and remained negative for over a year. Following a treatment break, low-level ctDNA positivity (1 and 3 PPM) preceded imaging-confirmed recurrence and chemotherapy was resumed. These cases highlight how NeXT Personal detections <10 PPM can guide earlier clinical interventions in real-world practice. These data demonstrate the consistent performance of NPDx in challenging real world conditions with limited inputs. The data also indicate the importance of detections below both 100 PPM and 10 PPM in the clinical setting. Citation Format: Rachel Marty Pyke, Steven Dea, Sherif El-Refai, Fábio C. P. Navarro, Charles W. Abbott, Yi Chen, Janet Lai, Gabor Bartha, John M. Lyle, Jason Harris, Vijay Gunuganti, Sean M. Boyle, Richard O. Chen. Enhancing MRD detection through an ultrasensitive ctDNA test: Insights from real-world clinical data [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3845.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-3845
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 3845: Enhancing MRD detection through an ultrasensitive ctDNA test: Insights from real-world clinical data

Steven Dea, Charles W. Abbott, Gábor Bartha, Vijay Gunuganti et al.
Cancer Research
Cancer Genomics and Diagnostics
article

Abstract 3845: Enhancing MRD detection through an ultrasensitive ctDNA test: Insights from real-world clinical data

Steven Dea, Charles W. Abbott, Gábor Bartha, Vijay Gunuganti, John Lyle, Sherif El-Refai, Rachel Marty Pyke, Sean M. Boyle, Janet Lai, Yi Chen, Fábio C. P. Navarro, Richard O. Chen, Jason Harris
article en

Abstract

Abstract There is a need for more sensitive circulating tumor DNA (ctDNA) tests that can achieve earlier detection of disease. The NeXT Personal Dx (NPDx) ctDNA MRD test utilizes a bespoke panel of up to ∼1800 variants to achieve ultrasensitive detection down to ∼1 part per million (PPM) of ctDNA with high analytical specificity (>99.9%). Here, we describe the real world performance from more than 5,000 patients profiled using NPDx. In this analysis we examined performance in a variety of real world testing situations and in the ultrasensitive range below 100PPM and 10 PPM, the latter of which has not been previously characterized. Overall, the median limit of detection (LOD) across all timepoints was 1.90 PPM (IQR:1.53-2.70 PPM) across 15 different cancer types. This performance was achieved with a relatively low median cell free DNA (cfDNA) input of 12ng (range 2-30 ng). 45.3% of tests were ctDNA positive overall. The NPDx tests performed well with challenging FFPE tumor samples (low tumor DIN <=3.4 or tumor fraction <=20%), achieving low LODs (median = 2.38 and 2.33 PPM, respectively). NPDx also achieved a median LOD of 3.78 PPM on low TMB tumors (<=0.98 mutation/MB). With ultra-low cfDNA inputs (<=5ng, 11.98% of cohort), NPDx achieved a median LOD of 2.31 PPM. Next we looked at performance in the ultrasensitive ranges below 100 PPM and 10 PPM. 40.2% of detections were in the ultrasensitive range below 100 PPM. Notably, 36.6% of all ultrasensitive detections were found to be <10 PPM (14.7% of detections overall), which aligned well with data from published NeXT Personal clinical studies (Lung - 42.5% in RWD, 40.5% in Black et. al 2025; Breast - 37.5% in RWD, 42.2% in Garcia-Murrillas et. al 2025). Detection rates <10 PPM were consistent across cfDNA input amounts down to 2 ng. For those patients who had sustained ctDNA positivity after a ctDNA negative timepoint, 49% had their first MRD+ detection <10 PPM. Two case studies demonstrate the clinical value of detections below 10 PPM in patient management. A 68-year-old female with squamous NSCLC underwent left upper lobectomy and MRD monitoring with NPDx. After three negative results, two low-level positives (6.2 and 9 PPM) prompted PET imaging that revealed a surgical-site recurrence. ctDNA rose to 80 PPM on the day of imaging, and radiation therapy led to ctDNA clearance. A 67-year-old female with colorectal cancer treated with FOLFOX + Avastin achieved ctDNA clearance and remained negative for over a year. Following a treatment break, low-level ctDNA positivity (1 and 3 PPM) preceded imaging-confirmed recurrence and chemotherapy was resumed. These cases highlight how NeXT Personal detections <10 PPM can guide earlier clinical interventions in real-world practice. These data demonstrate the consistent performance of NPDx in challenging real world conditions with limited inputs. The data also indicate the importance of detections below both 100 PPM and 10 PPM in the clinical setting. Citation Format: Rachel Marty Pyke, Steven Dea, Sherif El-Refai, Fábio C. P. Navarro, Charles W. Abbott, Yi Chen, Janet Lai, Gabor Bartha, John M. Lyle, Jason Harris, Vijay Gunuganti, Sean M. Boyle, Richard O. Chen. Enhancing MRD detection through an ultrasensitive ctDNA test: Insights from real-world clinical data [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3845.

Cancer ResearchVol. 86(7_Supplement)
Personalis (United States) (US)
Openalex Percentile: Top 32%
Cancer Genomics and Diagnostics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.