Evidence map›Paper›PMID 39444426›Full record

ArticleTherapeutic advances in medical oncology2024

BLU-945, a potent and selective next-generation EGFR TKI, has antitumor activity in models of osimertinib-resistant non-small-cell lung cancer.

Sun Min Lim, Stefanie S Schalm, Eun Ji Lee, Sewon Park, Chiara Conti, Yves A Millet, Rich Woessner, Zhuo Zhang, Luz E Tavera-Mendoza, Faith Stevison and 10 more

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2024. 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
–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

15 citing papers in PubMed.

  1. Targeting ClassicalCancers · 2026
    Review
  2. Article
  3. JIN-A02, a Mutant-Selective Fourth-Generation EGFR Inhibitor, Overcomes C797S-Mediated Resistance and Demonstrates Intracranial Activity in NSCLC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  4. Review
  5. Fourth-generation EGFR-TKI to overcome C797S mutation: past, present, and future.Journal of enzyme inhibition and medicinal chemistry · 2025
    Review
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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

20 authors.

Sun Min LimDivision of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-7694-1593
Stefanie S SchalmBlueprint Medicines Corporation, Cambridge, MA, USA.
Eun Ji LeeDepartment of Biomedical Science Institute, Graduated School of Medical Science, Brain Korea 21 FOUR Project for Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-4362-939X
Sewon ParkJEUK Institute for Cancer Research, JEUK Co. Ltd., Seoul, Republic of Korea.
Chiara ContiBlueprint Medicines Corporation, Cambridge, MA, USA.
Yves A MilletBlueprint Medicines Corporation, Cambridge, MA, USA.
Rich WoessnerBlueprint Medicines Corporation, Cambridge, MA, USA.
Zhuo ZhangBlueprint Medicines Corporation, Cambridge, MA, USA.
Luz E Tavera-MendozaBlueprint Medicines Corporation, Cambridge, MA, USA.
Faith StevisonBlueprint Medicines Corporation, Cambridge, MA, USA.
Faris AlbayyaBlueprint Medicines Corporation, Cambridge, MA, USA.
Thomas A DineenBlueprint Medicines Corporation, Cambridge, MA, USA.
John HsiehBlueprint Medicines Corporation, Cambridge, MA, USA.
Seung Yeon OhDepartment of Biomedical Science Institute, Graduated School of Medical Science, Brain Korea 21 FOUR Project for Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea.
Alena ZalutskayaBlueprint Medicines Corporation, Cambridge, MA, USA.
Julia RotowDana-Farber Cancer Institute, Boston, MA, USA.
Koichi GotoDepartment of Thoracic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Dae-Ho LeeDepartment of Oncology, Asan Medical Center University of Ulsan College of Medicine, Seoul, Republic of Korea.
Mi Ran YunSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Byoung Chul ChoDivision of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea.ORCID https://orcid.org/0000-0002-5562-270X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Despite the availability of several epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs), most patients with non-small-cell lung cancer (NSCLC) eventually develop resistance to these agents. Notably, Methods: In vitro activity of BLU-945 as a single agent and in combination with osimertinib was tested in engineered Results: In vitro BLU-945 demonstrated inhibited cell viability and growth of Conclusion: Our findings demonstrate the preclinical and early clinical activity of BLU-945 in

Indexed as

BLU-945clinical trial designdrug resistanceEGFREGFR inhibitorsNSCLCosimertinibpatient-derived xenograftTKI

Identifiers

PMID39444426
PMCPMC11497503

What OpenQuestion holds

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LicenceCC BY-NC
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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.