Evidence map›Paper›PMID 39028931›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2024

Neoadjuvant Osimertinib for the Treatment of Stage I-IIIA Epidermal Growth Factor Receptor-Mutated Non-Small Cell Lung Cancer: A Phase II Multicenter Study.

Collin M Blakely, Anatoly Urisman, Matthew A Gubens, Claire K Mulvey, Greg M Allen, Stephen C Shiboski, Julia K Rotow, Turja Chakrabarti, D Lucas Kerr, Jacqueline V Aredo and 14 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 3 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

57 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Neoadjuvant Osimertinib for ResectableJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Trial
  6. Trial
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Targeting ClassicalCancers · 2026
    Review
  15. Observational
  16. Article
  17. Article
  18. Article
  19. Review
  20. Targeted therapy for stage IA non-small cell lung cancer withTranslational lung cancer research · 2026
    Review
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

24 authors.

Collin M BlakelyDepartment of Medicine, University of California, San Francisco, San Francisco, CA.ORCID 0000-0001-8134-3651
Anatoly UrismanHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.ORCID 0000-0001-8364-5303
Matthew A GubensDepartment of Medicine, University of California, San Francisco, San Francisco, CA.
Claire K MulveyDepartment of Medicine, University of California, San Francisco, San Francisco, CA.
Greg M AllenDepartment of Medicine, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-0032-8140
Stephen C ShiboskiDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-9257-2609
Julia K RotowLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.
Turja ChakrabartiDepartment of Medicine, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-2966-3102
D Lucas KerrDepartment of Medicine, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-0557-8341
Jacqueline V AredoDepartment of Medicine, University of California, San Francisco, San Francisco, CA.ORCID 0000-0003-0559-3565
Bianca BacaltosHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-0824-6246
Megan GeeHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.
Lisa TanHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.
Kirk D JonesDepartment of Pathology, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-0275-3503
W Patrick DevineDepartment of Pathology, University of California, San Francisco, San Francisco, CA.
Robert C DoebeleDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO.
Dara L AisnerDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0001-5203-5932
Tejas PatilDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0003-4389-1010
Erin L SchenkDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0001-9418-9948
Trever G BivonaDepartment of Medicine, University of California, San Francisco, San Francisco, CA.ORCID 0000-0001-5734-4128
Jonathan W RiessDepartment of Medicine, University of California Davis, Sacramento, CA.
Melissa ColemanHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.
Johannes R KratzHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.ORCID 0000-0003-0696-4073
David M JablonsHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
UCSF Project 1U54CA224081 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Trever G Bivona, Jack Roth · 2017 to 2026
$12.9M
Stress responses drive resistance and shape tumor evolution in EGFR mutant lung cancerR01CA238236 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BIVONA, TREVER G · 2020 to 2024
$2.5M
NCI NIH HHS P30 CA093373NCI NIH HHS R01 CA238236NCI NIH HHS U54 CA224081
6 · The paper itself

Abstract

purposeTo assess the safety and efficacy of the third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor osimertinib as neoadjuvant therapy in patients with surgically resectable stage I-IIIA PATIENTS AND

methodsThis was a multi-institutional phase II trial of neoadjuvant osimertinib for patients with surgically resectable stage I-IIIA (American Joint Committee on Cancer [AJCC] V7)

resultsA total of 27 patients were enrolled and treated with neoadjuvant osimertinib for a median 56 days before surgical resection. Twenty-four (89%) patients underwent subsequent surgery; three (11%) patients were converted to definitive chemoradiotherapy. The MPR rate was 14.8% (95% CI, 4.2 to 33.7). No pathological complete responses were observed. The ORR was 52%, and the median DFS was 40.9 months. One treatment-related serious adverse event (AE) occurred (3.7%). No patients were unable to undergo surgical resection or had surgery delayed because of an AE. The most common co-occurring tumor genomic alterations were in

conclusionTreatment with neoadjuvant osimertinib in surgically resectable (stage IA-IIIA, AJCC V7)

Indexed as

AcrylamidesAniline CompoundsCarcinoma, Non-Small-Cell LungErbB ReceptorsLung NeoplasmsMutationNeoadjuvant TherapyAdultAgedAntineoplastic AgentsFemaleHumansIndolesMaleMiddle AgedNeoplasm StagingAcrylamidesAniline CompoundsAntineoplastic AgentsEGFR protein, humanErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidines

Identifiers

PMID39028931
PMCPMC11379363

What OpenQuestion holds

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Registered trials

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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.