Evidence map›Paper›PMID 28278193›Full record

ArticlePloS one2017

A BCR-ABL1 cutoff of 1.5% at 3 months, determined by the GeneXpert system, predicts an optimal response in patients with chronic myeloid leukemia.

Valentín García-Gutiérrez, María T Gómez-Casares, José M Puerta, Juan M Alonso-Domínguez, Santiago Osorio, Juan C Hernández-Boluda, Rosa Collado, María J Ramírez, Fátima Ibáñez, María L Martín and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. 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
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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

20 authors at 12 institutions in 1 country.

Valentín García-GutiérrezHematology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
María T Gómez-CasaresHematology Department, Hospital Universitario Doctor Negrín, Las Palmas de Gran Canaria, Spain.
José M PuertaUnidad de Gestión Clínica Hematología y Hemoterapia, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Juan M Alonso-DomínguezHospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Santiago OsorioHematology Department, Hospital Universitario Gregorio Marañón, Madrid, Spain.
Juan C Hernández-BoludaHematology Department, Hospital Clínico, Valencia, Spain.
Rosa ColladoGenetic Laboratory, Hematology Department, Consorcio Hospital General Universitario, Valencia, Spain.
María J RamírezHematology Department, Hospital de Jerez de la Frontera, Cádiz, Spain.
Fátima IbáñezHematology Department, Hospital San Pedro de Alcántara, Cáceres, Spain.
María L MartínHematology Department, Hospital Universitario Virgen Macarena, Sevilla, Spain.
Juan D Rodríguez-GambarteHematology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Carolina Martínez-LapercheHematology Department, Hospital Universitario Gregorio Marañón, Madrid, Spain.
Montse GómezHematology Department, Hospital Clínico, Valencia, Spain.
Dolly V FialloHematology Department, Hospital Universitario Doctor Negrín, Las Palmas de Gran Canaria, Spain.
Sara RedondoHematology Department, Hospital Universitario Gregorio Marañón, Madrid, Spain.
Alicia RodríguezHematology Department, Hospital Universitario Virgen Macarena, Sevilla, Spain.
Concepción Ruiz-NuñoHematology Department, Hospital Regional Universitario de Málaga, IBIMA, Málaga, Spain.
Juan L SteegmannHematology Department & IIS-IP, Hospital Universitario de la Princesa, Madrid, Spain.
Antonio Jiménez-VelascoHematology Department, Hospital Regional Universitario de Málaga, IBIMA, Málaga, Spain.ORCID http://orcid.org/0000-0001-6421-7872
Spanish Group of Chronic Myeloid Leukemia (GELMC)
Hospital General Universitario Gregorio Marañón · ESHospital Clínico Universitario de Valencia · ESHospital Regional Universitario de Málaga · ESHospital Universitario de Gran Canaria Doctor Negrín · ESHospital Universitario Ramón y Cajal · ESHospital Universitario Virgen Macarena · ESHospital General Universitario De Valencia · ESHospital Jerez Puerta del Sur · ESHospital San Pedro de Alcántara · ESHospital Universitario de La Princesa · ESHospital Universitario Fundación Jiménez Díaz · ESHospital Universitario Virgen de las Nieves · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In chronic myeloid leukemia (CML) patients, 3-month BCR-ABL1 levels have consistently been correlated with further outcomes. Monitoring molecular responses in CML using the GeneXpert (Cepheid) platform has shown an optimal correlation with standardized RQ-PCR (IS) when measuring BCR-ABL1 levels lower than 10%, as it is not accurate for values over 10%. The aim of the present study was to determine the predictive molecular value at three months on different outcome variables using the Xpert BCR-ABL1 MonitorTM assay (Xpert BCR-ABL1). We monitored 125 newly diagnosed consecutive CML patients in the chronic phase (CML-CP) using an automated method: Xpert BCR-ABL1. Only 5% of patients did not achieve an optimal response at 3 months, and the 10% BCR-ABL1 cutoff defined by RQ-PCR (IS) methods was unable to identify significant differences in the probabilities of achieving a complete cytogenetic response (CCyR) (50% vs. 87%, p = 0.1) or a major molecular response (MMR) (60% vs. 80%, p = 0.29) by 12 months. In contrast, a cutoff of 1.5% more accurately identified differences in the probabilities of achieving CCyR (98% vs. 54%, p<0.001) and MMR (88% vs. 56%, p<0.001) by 12 months, as well as probabilities of treatment changes (p = 0.005). Therefore, when using the Xpert BCR-ABL1 assay, a cutoff of 1.5% at 3 months could with high probability identify patients able to achieve an optimal response at 12 months.

Indexed as

AdultAgedBiomarkers, TumorCohort StudiesFemaleFollow-Up StudiesFusion Proteins, bcr-ablGene RearrangementHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedNeoplasm StagingPolymerase Chain ReactionPrognosisProtein Kinase InhibitorsBiomarkers, TumorFusion Proteins, bcr-ablProtein Kinase Inhibitors

Identifiers

PMID28278193
PMCPMC5344481
OpenAlexW2593398179

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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.