Evidence map›Paper›PMID 34261696›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Integrative Profiling of T790M-Negative EGFR-Mutated NSCLC Reveals Pervasive Lineage Transition and Therapeutic Opportunities.

Khi Pin Chua, Yvonne H F Teng, Aaron C Tan, Angela Takano, Jacob J S Alvarez, Rahul Nahar, Neha Rohatgi, Gillianne G Y Lai, Zaw Win Aung, Joe P S Yeong and 29 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.8field-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

28 citing papers in PubMed, 36 citations in OpenAlex.

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  10. EGFR: New Insights on Its Activation and Mutation in Tumor and Tumor Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  11. EGFR-TKIs Induced DPP4 Drives Metabolic Reprogramming of Persister Cells in Lung Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

39 authors at 7 institutions in 5 countries.

Khi Pin Chua *Genome Institute of Singapore, Singapore, Singapore.ORCID 0000-0002-0083-0181
Yvonne H F Teng *Division of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Aaron C Tan *Division of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.ORCID 0000-0001-7292-1114
Angela TakanoDivision of Pathology, Singapore General Hospital, Singapore, Singapore.ORCID 0000-0002-7830-8430
Jacob J S AlvarezGenome Institute of Singapore, Singapore, Singapore.
Rahul NaharGenome Institute of Singapore, Singapore, Singapore.
Neha RohatgiGenome Institute of Singapore, Singapore, Singapore.
Gillianne G Y LaiDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Zaw Win AungDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Joe P S YeongDivision of Pathology, Singapore General Hospital, Singapore, Singapore.
Kiat Hon LimDivision of Pathology, Singapore General Hospital, Singapore, Singapore.
Marjan Mojtabavi NaeiniGenome Institute of Singapore, Singapore, Singapore.ORCID 0000-0003-1422-1106
Irfahan KassamGenome Institute of Singapore, Singapore, Singapore.ORCID 0000-0002-6150-5614
Amit JainDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Wan Ling TanDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Apoorva GognaDepartment of Vascular and Interventional Radiology, Singapore General Hospital, Singapore, Singapore.
Chow Wei TooDepartment of Vascular and Interventional Radiology, Singapore General Hospital, Singapore, Singapore.
Ravindran KanesvaranDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.ORCID 0000-0002-2351-881X
Quan Sing NgDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Mei Kim AngDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Tanujaa RajasekaranDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Devanand AnanthamDepartment of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore, Singapore.ORCID 0000-0002-3375-1164
Ghee Chee PhuaDepartment of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore, Singapore.
Bien Soo TanDepartment of Vascular and Interventional Radiology, Singapore General Hospital, Singapore, Singapore.ORCID 0000-0003-3716-7501
Yin Yeng LeeGenome Institute of Singapore, Singapore, Singapore.
Lanying WangDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.ORCID 0000-0002-5414-0055
Audrey S M TeoGenome Institute of Singapore, Singapore, Singapore.
Alexis Jiaying KhngGenome Institute of Singapore, Singapore, Singapore.ORCID 0000-0003-1004-6048
Ming Jie LimGenome Institute of Singapore, Singapore, Singapore.
Lisda SutejaDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.ORCID 0000-0002-4548-2766
Chee Keong TohDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Wan-Teck LimDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.ORCID 0000-0002-4655-0206
N Gopalakrishna IyerCancer Therapeutics Research Laboratory, National Cancer Center Singapore, Singapore, Singapore.
Wai Leong TamGenome Institute of Singapore, Singapore, Singapore.ORCID 0000-0003-2365-5264
Eng-Huat TanDivision of Medical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Weiwei ZhaiGenome Institute of Singapore, Singapore, Singapore.
Axel M HillmerGenome Institute of Singapore, Singapore, Singapore.ORCID 0000-0002-3381-7266
Anders J Skanderup *Genome Institute of Singapore, Singapore, Singapore. daniel.tan.s.w@singhealth.com.sg skanderupamj@gis.a-star.edu.sg.
Daniel S W Tan *Genome Institute of Singapore, Singapore, Singapore. daniel.tan.s.w@singhealth.com.sg skanderupamj@gis.a-star.edu.sg.
National Cancer Centre Singapore · SGGenome Institute of Singapore · SGSingapore General Hospital · SGDuke-NUS Medical School · SGKunming Institute of Zoology · CNNational University of Singapore · SGUniversity Hospital Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDespite the established role of EGFR tyrosine kinase inhibitors (TKIs) in EXPERIMENTAL

designWe performed whole-exome and transcriptome analysis of 59 patients with first- and second-generation EGFR TKI-resistant metastatic

resultsTranscriptomic analysis revealed ubiquitous loss of adenocarcinoma lineage gene expression in T790M

conclusionsOur results illustrate the interplay between genetic alterations, cell lineage plasticity, and immune microenvironment in shaping divergent TKI resistance and outcome trajectories in

Indexed as

MutationCarcinoma, Non-Small-Cell LungErbB ReceptorsHumansLung NeoplasmsProtein-Tyrosine KinasesEGFR protein, humanErbB ReceptorsProtein-Tyrosine Kinases

Identifiers

PMID34261696
PMCPMC9401458
OpenAlexW3182408948

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.