Evidence map›Paper›PMID 35456982›Full record

ReviewInternational journal of molecular sciences2022

Morphologic-Molecular Transformation of Oncogene Addicted Non-Small Cell Lung Cancer.

Fiorella Calabrese, Federica Pezzuto, Francesca Lunardi, Francesco Fortarezza, Sofia-Eleni Tzorakoleftheraki, Maria Vittoria Resi, Mariaenrica Tiné, Giulia Pasello, Paul Hofman

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  15. Transformation ofTranslational lung cancer research · 2023
    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

9 authors at 3 institutions in 3 countries.

Fiorella CalabreseDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, 35128 Padova, Italy.
Federica PezzutoDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, 35128 Padova, Italy.ORCID 0000-0002-8023-3108
Francesca LunardiDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, 35128 Padova, Italy.ORCID 0000-0001-5792-4683
Francesco FortarezzaDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, 35128 Padova, Italy.ORCID 0000-0002-8954-5888
Sofia-Eleni TzorakoleftherakiDepartment of Pathology, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece.
Maria Vittoria ResiDepartment of Surgery, Oncology and Gastroenterology, University of Padova, 35128 Padova, Italy.
Mariaenrica TinéDepartment of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, 35128 Padova, Italy.
Giulia PaselloDepartment of Surgery, Oncology and Gastroenterology, University of Padova, 35128 Padova, Italy.
Paul HofmanLaboratoire de Pathologie Clinique et Expérimentale, FHU OncoAge, Biobank BB-0033-00025, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0003-0431-9353
University of Padua · ITAristotle University of Thessaloniki · GRUniversité Côte d'Azur · FR

Funding

University of Padova BIRD218739/21
6 · The paper itself

Abstract

Patients with non-small cell lung cancer, especially adenocarcinomas, harbour at least one oncogenic driver mutation that can potentially be a target for therapy. Treatments of these oncogene-addicted tumours, such as the use of tyrosine kinase inhibitors (TKIs) of mutated epidermal growth factor receptor, have dramatically improved the outcome of patients. However, some patients may acquire resistance to treatment early on after starting a targeted therapy. Transformations to other histotypes-small cell lung carcinoma, large cell neuroendocrine carcinoma, squamous cell carcinoma, and sarcomatoid carcinoma-have been increasingly recognised as important mechanisms of resistance and are increasingly becoming a topic of interest for all specialists involved in the diagnosis, management, and care of these patients. This article, after examining the most used TKI agents and their main biological activities, discusses histological and molecular transformations with an up-to-date review of all previous cases published in the field. Liquid biopsy and future research directions are also briefly discussed to offer the reader a complete and up-to-date overview of the topic.

Indexed as

AdenocarcinomaAntineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsDrug Resistance, NeoplasmHumansMutationOncogenesProtein Kinase InhibitorsAntineoplastic AgentsProtein Kinase Inhibitorsnon-small cell lung canceroncogene addictedsmall cell lung cancer

Identifiers

PMID35456982
PMCPMC9031930
OpenAlexW4223532888

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.