Evidence map›Paper›PMID 31026597›Full record

ArticleThe Journal of molecular diagnostics : JMD2019

Analytical Validation of a Highly Sensitive, Multiplexed Chronic Myeloid Leukemia Monitoring System Targeting BCR-ABL1 RNA.

Justin T Brown, Ion J Beldorth, Walairat Laosinchai-Wolf, Marie E Fahey, Keri L Jefferson, Adam K Ruskin, Jacquelyn J Roth, Li Cai, Christopher D Watt, Richard D Press and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. The Role and Diagnostic Efficacy of the METTL14/GADD45B mCellular and molecular neurobiology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
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

13 authors at 4 institutions in 1 country.

Justin T BrownAsuragen, Inc., Austin, Texas. Electronic address: jbrown@asuragen.com.
Ion J BeldorthAsuragen, Inc., Austin, Texas.
Walairat Laosinchai-WolfAsuragen, Inc., Austin, Texas.
Marie E FaheyAsuragen, Inc., Austin, Texas.
Keri L JeffersonAsuragen, Inc., Austin, Texas.
Adam K RuskinAsuragen, Inc., Austin, Texas.
Jacquelyn J RothDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
Li CaiCenter for Molecular Biology and Pathology, Laboratory Corporation of America Holdings, Research Triangle Park, North Carolina.
Christopher D WattDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
Richard D PressDepartment of Pathology and Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
Fei YangDepartment of Pathology and Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
John B HedgesAsuragen, Inc., Austin, Texas.
Bernard F AndrussAsuragen, Inc., Austin, Texas.
Asuragen (United States) · USHospital of the University of Pennsylvania · USOregon Health & Science University · USLabCorp (United States) · US

Funding

NCI NIH HHS HHSN261201500009C
6 · The paper itself

Abstract

This study describes the analytical performance of the QuantideX qPCR BCR-ABL IS Kit, the first Food and Drug Administration-cleared assay designed to monitor breakpoint cluster region-Abelson tyrosine-protein kinase 1 (BCR-ABL1) fusion transcripts isolated from peripheral blood specimens from patients with chronic myeloid leukemia. This multiplex real-time quantitative RT-PCR assay amplifies both e13a2 and e14a2 Major BCR-ABL1 transcripts and the reference target ABL1. The test results are provided in international scale (IS) values by incorporating armored RNA-based calibrators that have defined IS values tied directly to the World Health Organization BCR-ABL1 Primary Reference Materials, without the necessity of determining and maintaining conversion factors. For each batch run, the integrated interpretive software evaluates run and specimen quality control metrics (including a sufficient amount of ABL1 control transcripts to ensure a minimal limit of detection) and calculates both molecular response (MR) and %IS values for each specimen. The test has a limit of detection of MR4.7 (0.002%IS) and a linear range from MR0.3 (50%IS) to MR4.7 (0.002%IS) for both Major transcripts. Single-site and multisite precision studies demonstrated a maximum SD of 0.13 MR (30% CV within the assay range between MR0.7 and MR3.7). The performance of this BCR-ABL1 monitoring test meets all of the clinical guideline recommendations for sensitivity and IS reporting for the management of chronic myeloid leukemia patients.

Indexed as

Multiplex Polymerase Chain ReactionReal-Time Polymerase Chain ReactionAllelesFusion Proteins, bcr-ablHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLod ScoreReproducibility of ResultsSensitivity and SpecificityFusion Proteins, bcr-abl

Identifiers

PMID31026597
PMCPMC6626993
OpenAlexW2942438975

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.