Evidence map›Paper›PMID 32151666›Full record

ReviewPharmacology & therapeutics2020

Acquired resistance to targeted therapies in NSCLC: Updates and evolving insights.

Catherine B Meador, Aaron N Hata

Abstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing 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

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

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8 more citing papers are in PubMed but not listed here.

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

2 authors.

Catherine B MeadorMassachusetts General Hospital Cancer Center, Charlestown, MA, USA; Dana Farber Cancer Institute, Boston, MA, USA.
Aaron N HataMassachusetts General Hospital Cancer Center, Charlestown, MA, USA; Department of Medicine, Harvard Medical School, Boston, MA, USA. Electronic address: ahata@mgh.harvard.edu.

Funding

Evolution of resistance of EGFR mutant non-small cell lung cancerK08CA197389 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HATA, AARON N · 2016 to 2020
$896k
NCI NIH HHS K08 CA197389
6 · The paper itself

Abstract

While significant advancements have been made in the available therapies for metastatic non-small cell lung cancer (NSCLC), acquired resistance remains a major barrier to treatment. We have not yet achieved the ability to cure advanced NSCLC with systemic therapy, despite our growing understanding of many of the oncogenic drivers of this disease. Rather, the emergence of drug-tolerant and drug-resistant cells remains the rule, even in the face of increasingly potent targeted therapies. In this review, we provide a broad overview of the mechanisms of resistance to targeted therapy that have been demonstrated across molecular subtypes of NSCLC, highlighting the dynamic interplay between driver oncogene, bypass signaling pathways, shifting cellular phenotypes, and surrounding tumor microenvironment.

Indexed as

Drug Resistance, NeoplasmAnimalsAntineoplastic AgentsBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell LineageHumansLung NeoplasmsMolecular Targeted TherapyTreatment OutcomeTumor MicroenvironmentAntineoplastic AgentsBiomarkers, TumorAcquired resistanceNon-small cell lung cancer (NSCLC)Targeted therapiesTumor microenvironment

Identifiers

PMID32151666
PMCPMC8675642

What OpenQuestion holds

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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.