Evidence map›Paper›PMID 32875515›Full record

ArticleMolecular diagnosis & therapy2020

Comparison of Droplet Digital PCR versus qPCR Measurements on the International Scale for the Molecular Monitoring of Chronic Myeloid Leukemia Patients.

Alicia Arenas Cortés, Susana Olmedillas, Juana Serrano-López, Daniel Lainez-González, Tamara Castaño, Rodrigo Iñiguez, José Luis Lopez-Lorenzo, Amanda García, Mireia Atance, Rocío Nieves Salgado Sánchez and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular diagnosis & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. 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

14 authors.

Alicia Arenas CortésExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Susana OlmedillasNew Therapy Group, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Madrid, Spain.
Juana Serrano-LópezExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Daniel Lainez-GonzálezExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.ORCID 0000-0002-2726-1193
Tamara CastañoExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Rodrigo IñiguezHematology Department, Doce de Octubre University Hospital, Madrid, Spain.
José Luis Lopez-LorenzoExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Amanda GarcíaHematology Department, Fundación Jiménez Díaz University Hospital, Madrid, Spain.
Mireia AtanceExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Rocío Nieves Salgado SánchezExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Carlos Blas LopezExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Mariano García ArranzNew Therapy Group, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Madrid, Spain.
Pilar Llamas SilleroExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain.
Juan Manuel Alonso-DominguezExperimental Hematology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain. juan.adominguez@fjd.es.ORCID 0000-0001-6233-5912

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBCR-ABL1/ABL1 p210 measurement by quantitative polymerase chain reaction (qPCR) is used worldwide to monitor the molecular response in chronic myeloid leukemia (CML) patients. Droplet digital polymerase chain reaction (ddPCR) seems to show a greater sensitivity than qPCR, probably due to the high number of replicates analyzed in ddPCR for the comparison. Additionally, in a recently published comparison, ddPCR measurements were not adequately transformed into International Scale (IS).

methodWe have analyzed 50 CML patients and ten non-CML donors in parallel by qPCR and ddPCR. To the best of our knowledge, this is the first study comparing both techniques under similar conditions, with BCR-ABL1/ABL1 measurements performed via both techniques transformed into IS.

resultsQualitative and quantitative comparisons showed excellent results. The qualitative correlation showed a Kappa index of 0.94 (95% confidence interval [CI] 0.90-0.98) (P < 0.001). In the quantitative comparison, the absolute intra-class correlation coefficient was 0.868 (95% CI 0.734-0.937; P < 0.001), and Lin's concordance correlation coefficient was 0.863. The Passing-Bablock test indicated a slight proportional difference between qPCR and ddPCR. A quantitative and qualitative subanalysis including 40 patients with a molecular response of 3.0 or deeper showed similar results in every test. In addition, the proportional difference in the Passing-Bablock test disappeared. There were no differences in the sensitivity for BCR-ABL1 detection between qPCR and ddPCR (McNemar test, P = 0.5).

conclusionsIn conclusion, our results show very good quantitative and qualitative correlations between BCR-ABL1/ABL1 p210 results obtained by qPCR and by ddPCR and confirm previous scarce data regarding the lack of an increase in sensitivity of ddPCR over qPCR in this setting.

Indexed as

AllelesBiomarkers, TumorFusion Proteins, bcr-ablGene FrequencyHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveReal-Time Polymerase Chain ReactionReproducibility of ResultsSensitivity and SpecificityBiomarkers, TumorFusion Proteins, bcr-abl

Identifiers

What OpenQuestion holds

Textmetadata
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.