Evidence map›Paper›PMID 41212866›Full record

ArticlePloS one2025

Analytical validation of a hybrid-approach combining tumor-informed and tumor-agnostic bespoke ctDNA panel assay for the sensitive detection of minimal residual disease.

Sunghoon Heo, Seon-Kyu Ham, Hayoon Lee, Bom Han, Hanseong Roh, Seongmun Jeong, Hwang-Phill Kim, Duhee Bang, Sang-Hyun Song, Tae-You Kim

Abstract readValidation Study
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sunghoon HeoIMBdx, Inc., Seoul, Korea.
Seon-Kyu HamIMBdx, Inc., Seoul, Korea.
Hayoon LeeIMBdx, Inc., Seoul, Korea.
Bom HanIMBdx, Inc., Seoul, Korea.
Hanseong RohIMBdx, Inc., Seoul, Korea.
Seongmun JeongIMBdx, Inc., Seoul, Korea.
Hwang-Phill KimIMBdx, Inc., Seoul, Korea.
Duhee BangDepartment of Chemistry, Yonsei University, Seoul, Korea.
Sang-Hyun SongIMBdx, Inc., Seoul, Korea.
Tae-You KimIMBdx, Inc., Seoul, Korea.ORCID https://orcid.org/0000-0002-9986-2684

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Minimal residual disease (MRD) is a small group of cancer cells not eliminated by anti-cancer treatment. Because of its small size, conventional imaging system may not be able to detect the MRD in routine clinical practice. Although the liquid biopsy tests can detect the circulating tumor DNA (ctDNA) when the tumor is present in the body, the fraction of ctDNA is considered lower than the 0.01% which is unreachable by current state-of-the-art liquid biopsy assay relying on fixed-gene panel approach. Here, we describe the analytical validation result of our previously developed a tumor-informed MRD test, CancerDetectTM (formerly reported as AlphaLiquid®Detect), leveraging large-scale mutation spectrum profiling strategy to enhance detection sensitivity. The CancerDetectTM is a hybrid-approach MRD test combining both personalized (bespoke) mutations and tumor-agnostic clinically actionable targets (hotspot mutations) with hybridization capture technology. The analytical validation result of CancerDetectTM showed limit of detection successfully reached down to 0.001% (10-5) with 99.9% specificity.

Indexed as

Circulating Tumor DNANeoplasm, ResidualNeoplasmsBiomarkers, TumorHumansLiquid BiopsyMutationSensitivity and SpecificityBiomarkers, TumorCirculating Tumor DNA

Identifiers

PMID41212866
PMCPMC12599964

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.