Evidence map›Paper›PMID 30217489›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2019

A Brief Report of Transformation From NSCLC to SCLC: Molecular and Therapeutic Characteristics.

Léonie Ferrer, Matteo Giaj Levra, Marie Brevet, Martine Antoine, Julien Mazieres, Giulio Rossi, Rita Chiari, Virginie Westeel, Michel Poudenx, Jacques Letreut and 6 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 1 pooled it
–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

83 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. JTO clinical and research reports · 2026
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23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Léonie FerrerThoracic Oncology unit, PTV, CHU Grenoble CS10217-38043 Grenoble cedex 9, France et INSERM U 823.
Matteo Giaj LevraThoracic Oncology unit, PTV, CHU Grenoble CS10217-38043 Grenoble cedex 9, France et INSERM U 823; Oncology Department, University of Turin, AOU San Luigi Gonzaga, Orbassano, Italy.
Marie BrevetService de pathologie Est, Hopital Louis Pradel, Lyon, France.
Martine AntoineService de pathologie, HU-Est Parisien site Tenon APHP, Paris, France.
Julien MazieresService de pneumologie Hôpital Rangueil, CHU de Toulouse, Toulouse, France.
Giulio RossiPathology Unit, Azienda della Romagna, Hospital Santa Maria delle Croci, Ravenna, Italy.
Rita ChiariOncology Unit, "Santa Maria della Misericordia" Hospital, Perugia, Italy.
Virginie WesteelService de pneumologie CHU, Jean Minjoz Besançon, France.
Michel PoudenxCentre Antoine Lacassagne, Nice, France.
Jacques LetreutService de pneumologie CH du Pays d'Aix, Aix-en-Provence, France.
Radj GervaisCRLCC Francois Baclesse, Caen, France.
Giorgia OsmanPulmonary Oncology Unit, St. Camillo Forlanini Hospital, Rome, Italy.
Nicolas GirardUniv Lyon 1, Univ Lyon, Lyon, France; Institut Curie, Institut du Thorax Curie Montsouris, Paris, France.
Anne Claire ToffartPathology Department, University of Turin, AOU San Luigi Gonzaga, Orbassano, Italy.
Silvia NovelloOncology Department, University of Turin, AOU San Luigi Gonzaga, Orbassano, Italy.
Denis Moro-SibilotThoracic Oncology unit, PTV, CHU Grenoble CS10217-38043 Grenoble cedex 9, France et INSERM U 823. Electronic address: DMoro.pneumo@chu-grenoble.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHistologic transformation from NSCLC to SCLC is a mechanism of resistance in EGFR-mutant tumors but is also occasionally observed in nonmutated NSCLC.

methodsWe performed a multicenter retrospective collection of cases presenting between 2005 and 2017. The objectives were to analyze survival data and to define epidemiologic, clinical, treatment and histomolecular characteristics at both the time of diagnosis of NSCLC and of SCLC.

resultsForty-eight EGFR-mutant NSCLC and 13 non-EGFR-mutant cases were registered. Most EGFR-mutant tumors retained the same EGFR mutation after transformation. The median time to SCLC transformation was shorter in the EGFR-mutant group than in non-EFGR mutants (16 months versus 26 months (p = 0.01)). Both tumors were responsive to platinum etoposide regimens (45% partial response for the EGFR-mutant group versus 40% for non-EFGR mutants). The median overall survival rates were 28 months in the EGFR-mutant group versus 37 months in the non-EFGR-mutant group, respectively. After transformation, the median overall survival was 9 months in the non-EGFR-mutant group versus 10 months in the EGFR-mutant group.

conclusionsTransformation into SCLC seems to occur more quickly in EGFR mutated tumors; however, once the tumor is transformed its survival and response to treatment seems comparable to that of classical SCLC.

Indexed as

Carcinoma, Non-Small-Cell LungFemaleHumansLung NeoplasmsMaleRetrospective StudiesSmall Cell Lung CarcinomaAdenocarcinomaEGFR mutationHistologic transformationSCLC

Identifiers

What OpenQuestion holds

Textmetadata
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.