Evidence map›Paper›PMID 29382302›Full record

ArticleBMC cancer2018

Clinical management and outcome of patients with advanced NSCLC carrying EGFR mutations in Spain.

Edurne Arriola, Ramón García Gómez, Pilar Diz, Margarita Majem, Maite Martínez Aguillo, Javier Valdivia, Alfredo Paredes, José Miguel Sánchez-Torres, Sergio Peralta Muñoz, Isidoro Barneto and 9 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. RELAY Subgroup Analyses by EGFR Ex19del and Ex21L858R Mutations for Ramucirumab Plus Erlotinib in Metastatic Non-Small Cell Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Trial
  3. Observational
  4. Article
  5. Article
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  8. 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

19 authors at 19 institutions in 1 country.

Edurne ArriolaMedical Oncology Department, Hospital del Mar, Passeig Marítim, 25-29, 08018, Barcelona, Spain. earriola@parcdesalutmar.cat.
Ramón García GómezHospital General Universitario Gregorio Marañón, Madrid, Spain.
Pilar DizHospital Universitario de León, León, Spain.
Margarita MajemHospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Maite Martínez AguilloComplejo Hospitalario de Navarra, Pamplona, Spain.
Javier ValdiviaHospital Universitario Virgen de las Nieves, Granada, Spain.
Alfredo ParedesHospital Universitario Donostia, San Sebastián, Spain.
José Miguel Sánchez-TorresHospital Universitario de La Princesa, Madrid, Spain.
Sergio Peralta MuñozHospital Universitari Sant Joan de Reus, Reus, Tarragona, Spain.
Isidoro BarnetoHospital Universitario Reina Sofía, Córdoba, Spain.
Vanesa GutierrezHospital Regional Universitario Carlos Haya, Málaga, Spain.
Jesús Manuel Andrade SantiagoHospital Virgen de la Salud, Toledo, Spain.
Francisco AparisiHospital Virgen de los Lirios, Alcoy, Alicante, Spain.
Dolores IslaHospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.
Santiago PonceHospital Universitario 12 de Octubre, Madrid, Spain.
David Vicente BazHospital Universitario Virgen Macarena, Sevilla, Spain.
Angel ArtalHospital Universitario Miguel Servet, Zaragoza, Spain.
Mariluz AmadorAstraZeneca, Madrid, Spain.
Mariano ProvencioHospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
AstraZeneca (Spain) · ESBiogipuzkoa Health Research Institute · ESComplejo Hospitalario de Navarra · ESHospital Clínico Universitario Lozano Blesa · ESHospital de León · ESHospital Del Mar · ESHospital de Sant Pau · ESHospital General Universitario Gregorio Marañón · ESHospital Regional Universitario de Málaga · ESHospital Universitario 12 De Octubre · ESHospital Universitario de La Princesa · ESHospital Universitario Miguel Servet · ESHospital Universitario Puerta de Hierro Majadahonda · ESHospital Universitario Reina Sofía · ESHospital Universitario Virgen de las Nieves · ESHospital Universitario Virgen Macarena · ESHospital Universitari Sant Joan de Reus · ESHospital Virgen de la Salud · ESHospital Virgen de los Lirios · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough the benefit of first-line epidermal growth factor receptor (EGFR) tyrosine-kinase inhibitors (TKIs) over chemotherapy has been demonstrated in several clinical trials, data from clinical practice is lacking and the optimal EGFR TKI to be used remains unclear. This study aims to assess the real-life diagnostic and clinical management and outcome of patients with advanced non-small-cell lung cancer (NSCLC) carrying EGFR mutations in Spain.

methodsAll consecutive patients recently diagnosed with advanced or metastatic NSCLC from April 2010 to December 2011 in 18 Spanish hospitals and carrying EGFR mutations were retrospectively evaluated.

resultsBetween March and November 2013, a total of 187 patients were enrolled (98.3% Caucasian, 61.9% female, 54.9% never-smokers, 89.0% adenocarcinoma). Mutation testing was mainly performed on biopsy tumour tissue specimens (69.0%) using a qPCR-based test (90%) (47.0% Therascreen EGFR PCR Kit). Common sensitising mutations were detected in 79.8% of patients: 57.1% had exon 19 deletions and 22.6% exon 21 L858R point mutations. The vast majority of patients received first-line therapy (n = 168; 92.8%). EGFR TKIs were the most commonly used first-line treatment (81.5%), while chemotherapy was more frequently administered as a second- and third-line option (51.9% and 56.0%, respectively). Of 141 patients who experienced disease progression, 79 (56.0%) received second-line treatment. After disease progression on first-line TKIs (n = 112), 33.9% received chemotherapy, 8.9% chemotherapy and a TKI, and 9.8% continued TKI therapy. Most patients received first-line gefitinib (83.0%), while erlotinib was more frequently used in the second-line setting (83.0%). Progression-free survival (PFS) and overall survival (OS) in patients harbouring common mutations were 11.1 months and 20.1 months respectively (exon 19 deletions: 12.4 and 21.4 months; L858R: 8.3 and 14.5 months), and 3.9 months and 11.1 months respectively for those with rare mutations.

conclusionEGFR TKIs (gefitinib and erlotinib) are used as the preferred first-line treatment while chemotherapy is more frequently administered as a second- and third-line option in routine clinical practice in Spain. In addition, efficacy data obtained in the real-life setting seem to concur with data from EGFR TKI phase III pivotal studies in NSCLC.

Indexed as

AgedCarcinoma, Non-Small-Cell LungDisease-Free SurvivalErbB ReceptorsErlotinib HydrochlorideFemaleGefitinibHumansMaleMiddle AgedMutationNeoplasm StagingProtein Kinase InhibitorsQuinazolinesSpainTreatment OutcomeEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideGefitinibProtein Kinase InhibitorsQuinazolinesChemotherapyClinical managementEGFR tyrosine kinase inhibitors (TKIs)Epidermal growth factor receptor (EGFR) gene mutationNon-small-cell lung cancer (NSCLC)

Identifiers

PMID29382302
PMCPMC5791371
OpenAlexW2794266462

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.