Evidence map›Paper›PMID 28445990›Full record

ArticleOncotarget2017

Prognostic value of tumor mutations in radically treated locally advanced non-small cell lung cancer patients.

Angela Boros, Ludovic Lacroix, Benjamin Lacas, Julien Adam, Jean-Pierre Pignon, Caroline Caramella, David Planchard, Vincent de Montpreville, Eric Deutsch, Antonin Levy and 2 more

Abstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Early-stage anaplastic lymphoma kinase (Translational lung cancer research · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. 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

12 authors.

Angela BorosRadiation Oncology Department, Gustave Roussy, Villejuif, France.
Ludovic LacroixBiopathology Department, Gustave Roussy, Villejuif, France.
Benjamin LacasBiostatistics and Epidemiolgy Unit, Villejuif, France.
Julien AdamBiopathology Department, Gustave Roussy, Villejuif, France.
Jean-Pierre PignonBiostatistics and Epidemiolgy Unit, Villejuif, France.
Caroline CaramellaImaging Department, Gustave Roussy, Villejuif, France.
David PlanchardMedical Oncology Department, Gustave Roussy, Villejuif, France.
Vincent de MontprevillePathology Department, Marie Lannelongue, Le Plessis Robinson, France.
Eric DeutschRadiation Oncology Department, Gustave Roussy, Villejuif, France.
Antonin LevyRadiation Oncology Department, Gustave Roussy, Villejuif, France.
Benjamin BesseMedical Oncology Department, Gustave Roussy, Villejuif, France.
Cécile Le PechouxRadiation Oncology Department, Gustave Roussy, Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChemo-radiation is standard treatment in locally advanced non-small cell lung cancers (NSCLC). The prognostic value of mutations has been poorly explored in this population.

resultsClinical data were collected from 190 patients and mutational profiles were obtained in 78 of them; 58 (74%) were males, 31 (40%) current smokers, 47/31 stage IIIA/IIIB and 40 (51%) adenocarcinoma. The following mutations were identified: EGFR 12% (9/78), KRAS 15% (12/78), BRAF 5% (3/65), PI3KCA 2% (1/57), NRAS 3% (1/32), and ALK+ (FISH) 4% (2/51). HER2 was not detected. Median follow-up was 3.1 years. Overall survival was evaluated by group; no significant differences were identified in median overall survival (p = 0.21), with 29.4 months for the EGFR/ALK group (n = 11), 12.8 months for other mutations (n = 17), and 23.4 months for wild-type (n = 50). The EGFR/ALK and other mutations groups had poorer median progression-free survival (9.6 and 6.0 months) compared to the wild-type group (12.0 months; multivariate hazard ratio 2.0 [95% CI, 0.9-4.2] and 2.8 [95% CI, 1.5-5.2] respectively, p = 0.003). MATERIALS AND

methodsWe retrospectively reviewed all patients receiving radical treatment for locally advanced NSCLC in a single institution between January 2002 and June 2013. Next generation sequencing was performed on DNA from paraffin-embedded tissue. ALK rearrangements were detected by immunohistochemistry and/or FISH. Mutational prognostic value for Kaplan-Meier survival parameters was determined by log-rank tests and Cox proportional hazards models.

conclusionsSelected gene alterations may be associated with poorer progression-free survival in locally advanced radically treated NSCLC and their prognostic and/or predictive value merits further evaluation in a larger population.

Indexed as

Biomarkers, TumorMutationAdultAgedCarcinoma, Non-Small-Cell LungCombined Modality TherapyDatabases, FactualDNA Mutational AnalysisFemaleHumansKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedNeoplasm StagingPrognosisBiomarkers, Tumorchemotherapylocally advancedmutationnon-small cell lung cancerprognostic

Identifiers

PMID28445990
PMCPMC5421921

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.