Evidence map›Paper›PMID 26993607›Full record

ArticleOncotarget2016

The comparison of outcomes from tyrosine kinase inhibitor monotherapy in second- or third-line for advanced non-small-cell lung cancer patients with wild-type or unknown EGFR status.

Giuseppe Bronte, Tindara Franchina, Massimiliano Alù, Giovanni Sortino, Claudia Celesia, Francesco Passiglia, Giuseppina Savio, Agata Laudani, Alessandro Russo, Antonio Picone and 8 more

Abstract readComparative Study
In one paragraph

Article in Oncotarget, 2016. 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. Article
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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

18 authors.

Giuseppe BronteDepartment of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
Tindara FranchinaMedical Oncology Unit-AOOR Papardo-Piemonte, Messina and Department of Human Pathology, University of Messina, Messina, Italy.
Massimiliano AlùMedical Oncology Unit, A.R.N.A.S. Civico, Palermo, Italy.
Giovanni SortinoDepartment of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
Claudia CelesiaDepartment of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
Francesco PassigliaDepartment of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
Giuseppina SavioMedical Oncology Unit, A.R.N.A.S. Civico, Palermo, Italy.
Agata LaudaniMedical Oncology Unit, A.R.N.A.S. Civico, Palermo, Italy.
Alessandro RussoMedical Oncology Unit-AOOR Papardo-Piemonte, Messina and Department of Human Pathology, University of Messina, Messina, Italy.
Antonio PiconeMedical Oncology Unit-AOOR Papardo-Piemonte, Messina and Department of Human Pathology, University of Messina, Messina, Italy.
Sergio RizzoDepartment of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
Michele De TursiDepartment of Medical, Oral and Biotechnological Sciences, University "G. D'Annunzio", Chieti, Italy.
Elisabetta GambaleDepartment of Medical, Oral and Biotechnological Sciences, University "G. D'Annunzio", Chieti, Italy.
Viviana BazanDepartment of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
Clara NatoliDepartment of Medical, Oral and Biotechnological Sciences, University "G. D'Annunzio", Chieti, Italy.
Livio BlasiMedical Oncology Unit, A.R.N.A.S. Civico, Palermo, Italy.
Vincenzo AdamoMedical Oncology Unit-AOOR Papardo-Piemonte, Messina and Department of Human Pathology, University of Messina, Messina, Italy.
Antonio RussoDepartment of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSecond-line treatment for advanced non-small-cell lung cancer (NSCLC) patients includes monotherapy with a third-generation cytotoxic drug (CT) or a tyrosine kinase inhibitor (TKI). These options are the actual standard for EGFR wild-type (WT) status, as patients with EGFR mutations achieve greater benefit by the use of TKI in first-line treatment. Some clinical trials and meta-analyses investigated the comparison between CT and TKI in second-line, but data are conflicting.

methodsWe designed a retrospective trial to gather information about TKI sensitivity in comparison with CT. We selected from clinical records patients treated with at least 1 line of CT and at least 1 line of TKI. We collected data about age, sex, performance status, comorbidity, smoking status, histotype, metastatic sites, EGFR status, treatment schedule, better response and time-to-progression (TTP) for each line of treatment and overall survival (OS).

results93 patients met selection criteria. Mean age 66,7 (range: 46-84). M/F ratio is 3:1. 39 EGFR-WT and 54 EGFR-UK. All patients received erlotinib or gefitinib as second-line treatment or erlotinib as third-line treatment. No TTP differences were observed for both second-line (HR:0,91; p = 0,6333) and third-line (HR:1.1; p = 0,6951) treatment (TKI vs CT). A trend of a benefit in OS in favor of 3rd-line TKI (HR:0,68; p = 0,11).

conclusionsThis study explores the role of TKIs in EGFR non-mutated NSCLC patients. OS analysis highlights a trend to a benefit in patients who received TKI in third-line, even if this result is statistically non-significant. Further analysis are needed to find an explanation for this observation.

Indexed as

AgedAged, 80 and overCarcinoma, Non-Small-Cell LungErbB ReceptorsErlotinib HydrochlorideFemaleGefitinibHumansKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedMutationProtein Kinase InhibitorsQuinazolinesRetrospective StudiesErbB ReceptorsErlotinib HydrochlorideGefitinibProtein Kinase InhibitorsQuinazolineschemotherapyEGFRnon-small-cell lung cancertyrosine kinase inhibitor

Identifiers

PMID26993607
PMCPMC5094963

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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.