Evidence map›Paper›PMID 35522668›Full record

ArticlePloS one2022

The efficacy of T790M mutation testing in liquid biopsy-Real clinic data.

Paweł Krawczyk, Luiza Grzycka-Kowalczyk, Justyna Błach, Katarzyna Reszka, Izabela Chmielewska, Robert Kieszko, Magdalena Wójcik-Superczyńska, Michał Szczyrek, Tomasz Jankowski, Janusz Milanowski

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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 at 2 institutions in 1 country.

Paweł KrawczykDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Luiza Grzycka-KowalczykDepartment of Radiology and Nuclear Medicine, Independent Public Clinical Hospital no. 4 in Lublin, Lublin, Poland.
Justyna BłachDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.ORCID 0000-0003-4154-156X
Katarzyna ReszkaInstitute of Genetic and Immunology GENIM LCC in Lublin, Lublin, Poland.
Izabela ChmielewskaDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Robert KieszkoDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Magdalena Wójcik-SuperczyńskaDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Michał SzczyrekDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Tomasz JankowskiDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Janusz MilanowskiDepartment of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Medical University of Lublin · PL1 Military Clinical Hospital with Outpatient Clinic · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osimertnib is still widely used in the treatment of NSCLC patients who have previously received erlotinib, gefitinib or afatinib and have developed resistance to these drugs mediated by the T790M mutation in exon 20 of EGFR gene. We assessed the results of T790M mutation testing in liquid biopsy by Entrogen test and real-time PCR technique in routine clinical practice. Analysis was conducted in 73 plasma samples from 41 patients with locally advanced or metastatic lung adenocarcinoma treated with first- or second-generation of EGFR TKIs. We detected T790M mutation in 18 patients (43.9% of patients, 24.6% positive tests in 73 samples). The incidence of T790M mutation in liquid biopsy was significantly higher in patients with T3-T4 tumors compared to patients with T0-T2 tumors (p = 0.0368, χ2 = 4.36). Median PFS at the time of progression according to RECIST was significantly (p = 0.0444) higher in patients with T790M mutation than in patients without this mutation (22.5 vs. 15 months). Our results confirmed that T790M mutation is more often detected in patients with a large tumor spreading in the chest and with the long duration of response to first- or second generation of EGFR TKIs. The low sensitivity of the real-time PCR technique in T790M mutation detection could be partially compensated by repeating the tests.

Indexed as

Adenocarcinoma of LungErbB ReceptorsLung NeoplasmsProtein Kinase InhibitorsDrug Resistance, NeoplasmHumansLiquid BiopsyMutationErbB ReceptorsProtein Kinase Inhibitors

Identifiers

PMID35522668
PMCPMC9075651
OpenAlexW4229080616

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.