Evidence map›Paper›PMID 35117060›Full record

ArticleTranslational cancer research2019

Prospective analysis of liquid biopsies of advanced non-small cell lung cancer patients after progression to targeted therapies using GeneReader NGS platform.

Clara Mayo de Las Casas, Mónica Garzón-Ibañez, Núria Jordana-Ariza, Santiago Viteri-Ramírez, Irene Moya-Horno, Niki Karachaliou, Zaira Yeste, Raquel Campos, Sergi Villatoro, Ariadna Balada-Bel and 23 more

Abstract read
In one paragraph

Article in Translational cancer research, 2019. 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
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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

33 authors.

Clara Mayo de Las CasasLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Mónica Garzón-IbañezLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Núria Jordana-ArizaLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Santiago Viteri-RamírezDr Rosell Oncology Institute (IOR), Quirón Dexeus University Hospital, Barcelona, Spain.
Irene Moya-HornoDr Rosell Oncology Institute (IOR), QuironSalud group, General Hospital of Catalonia, Sant Cugat del Vallés, Spain.
Niki KarachaliouDr Rosell Oncology Institute (IOR), QuironSalud group, University Hospital Sagrat Cor, Barcelona, Spain.
Zaira YesteLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Raquel CamposLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Sergi VillatoroLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Ariadna Balada-BelLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Beatriz García-PeláezLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Noemí ReguartDepartment of Medical Oncology, Hospital Clínic, Barcelona, Spain.
Cristina TeixidóDepartment of Medical Oncology, Hospital Clínic, Barcelona, Spain.
Eloisa JantúsMolecular Oncology Laboratory, Fundación Investigación, Hospital General Universitario de Valencia, Valencia, Spain.
Silvia CalabuigMolecular Oncology Laboratory, Fundación Investigación, Hospital General Universitario de Valencia, Valencia, Spain.
Cristina AguadoLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Ana Giménez-CapitánLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Ruth Román-LladóLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Ana Pérez-RosadoLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Maria José CatalánLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Jordi Bertrán-AlamilloLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Silvia García-RománLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Sonia RodriguezLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Lidia AlonsoCellex Centre, Vall d'Hebrón, Institute of Oncology, Barcelona, Spain.
Erika AldeguerLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Alejandro Martínez-BuenoDr Rosell Oncology Institute (IOR), Quirón Dexeus University Hospital, Barcelona, Spain.
Maria González-CaoDr Rosell Oncology Institute (IOR), Quirón Dexeus University Hospital, Barcelona, Spain.
Andrés Aguilar HernandezDr Rosell Oncology Institute (IOR), Quirón Dexeus University Hospital, Barcelona, Spain.
Juan Garcia-MosqueraDr Rosell Oncology Institute (IOR), Quirón Dexeus University Hospital, Barcelona, Spain.
Maria de Los Llanos GilHospital Mateu Orfila, Menorca, Spain.
Manuel FernandezDr Rosell Oncology Institute (IOR), QuironSalud group, University Hospital Sagrat Cor, Barcelona, Spain.
Rafael RosellLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.
Miguel Ángel Molina-VilaLaboratory of Oncology, Pangaea Oncology, Quirón Dexeus University Hospital, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn a significant percentage of advanced non-small cell lung cancer (NSCLC) patients, tumor tissue is unavailable or insufficient for genetic analyses at time to progression. We prospectively analyzed the appearance of genetic alterations associated with resistance in liquid biopsies of advanced NSCLC patients progressing to targeted therapies using the NGS platform.

methodsA total of 24 NSCLC patients were included in the study, 22 progressing to tyrosine kinase inhibitors and two to other treatments. Liquid biopsies samples were obtained and analyzed using the GeneRead

resultsOf the 21 patients progressing to tyrosine kinase inhibitors with valid results in liquid biopsy, NGS analysis identified a potential mechanism of resistance in 12 (57%). The most common were acquired mutations in

conclusionsNGS analysis in liquid biopsies of patients progressing to targeted therapies using the GeneReader platform is feasible and can help the oncologist to make treatment decisions.

Indexed as

GeneReaderliquid biopsiesNon-small cell lung cancer (NSCLC)progression

Identifiers

PMID35117060
PMCPMC8797948

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LicenceCC BY-NC-ND
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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.