Evidence map›Paper›PMID 26327924›Full record

ReviewTherapeutic advances in medical oncology2015

Overcoming resistance to targeted therapies in NSCLC: current approaches and clinical application.

Paolo Maione, Paola Claudia Sacco, Assunta Sgambato, Francesca Casaluce, Antonio Rossi, Cesare Gridelli

Open access · greenAbstract readReview
In one paragraph

Review in Therapeutic advances in medical oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 57 citations in OpenAlex.

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  10. CRL2Oncogene · 2022
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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

6 authors at 2 institutions in 1 country.

Paolo MaioneDivision of Medical Oncology, 'S. G. Moscati' Hospital, Contrada Amoretta, Avellino, 83100, Italy.
Paola Claudia SaccoDivision of Medical Oncology, 'S. G. Moscati' Hospital, Avellino, Italy.
Assunta SgambatoDepartment of Clinical and Experimental Medicine, Second University of Naples, Naples, Italy.
Francesca CasaluceDepartment of Clinical and Experimental Medicine, Second University of Naples, Naples, Italy.
Antonio RossiDivision of Medical Oncology, 'S. G. Moscati' Hospital, Avellino, Italy.
Cesare GridelliDivision of Medical Oncology, 'S. G. Moscati' Hospital, Avellino, Italy.
Azienda Ospedaliera S.Giuseppe Moscati · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The discovery that a number of aberrant tumorigenic processes and signal transduction pathways are mediated by druggable protein kinases has led to a revolutionary change in nonsmall cell lung cancer (NSCLC) treatment. Epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) are the targets of several tyrosine kinase inhibitors (TKIs), some of them approved for treatment and others currently in clinical development. First-generation agents offer, in target populations, a substantial improvement of outcomes compared with standard chemotherapy in the treatment of advanced NSCLC. Unfortunately, drug resistance develops after initial benefit through a variety of mechanisms. Novel generation EGFR and ALK inhibitors are currently in advanced clinical development and are producing encouraging results in patients with acquired resistance to previous generation agents. The search for new drugs or strategies to overcome the TKI resistance in patients with EGFR mutations or ALK rearrangements is to be considered a priority for the improvement of outcomes in the treatment of advanced NSCLC.

Indexed as

alectinibALK rearrangementsAZD9291ceritinibCO-1686EGFR mutationsselective EGFR inhibitorsT790M

Identifiers

PMID26327924
PMCPMC4543855
OpenAlexW1934312149

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.