Evidence map›Paper›PMID 41175446›Full record

ArticleCancer treatment and research communications2025

Osimertinib retreatment for patients with advanced EGFR-mutated non-small cell lung cancer.

Kevin M Levine, Natalie F Uy, Ted A Gooley, Jenna Voutsinas, Micah Tratt, Keith D Eaton, Rafael Santana-Davila, Alice H Berger, Christina S Baik

Abstract read
In one paragraph

Article in Cancer treatment and research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

9 authors.

Kevin M LevineUniversity of Washington, Seattle, WA, USA; Fred Hutchinson Cancer Center, Seattle, WA, USA.
Natalie F UyUniversity of Washington, Seattle, WA, USA; Fred Hutchinson Cancer Center, Seattle, WA, USA.
Ted A GooleyFred Hutchinson Cancer Center, Seattle, WA, USA.
Jenna VoutsinasFred Hutchinson Cancer Center, Seattle, WA, USA.
Micah TrattFred Hutchinson Cancer Center, Seattle, WA, USA.
Keith D EatonUniversity of Washington, Seattle, WA, USA; Fred Hutchinson Cancer Center, Seattle, WA, USA.
Rafael Santana-DavilaUniversity of Washington, Seattle, WA, USA; Fred Hutchinson Cancer Center, Seattle, WA, USA.
Alice H BergerFred Hutchinson Cancer Center, Seattle, WA, USA.
Christina S BaikUniversity of Washington, Seattle, WA, USA; Fred Hutchinson Cancer Center, Seattle, WA, USA. Electronic address: cbaik2@uw.edu.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
TRAINING IN CANCER BIOLOGY &TRANSPLANTATIONT32CA009515 · NCI · UNIVERSITY OF WASHINGTON · PI NANCY ELLEN DAVIDSON, Effie W Petersdorf · 1985 to 2026
$16.2M
NCI NIH HHS P30 CA015704NCI NIH HHS T32 CA009515
6 · The paper itself

Abstract

Resistance to osimertinib, a third-generation EGFR tyrosine kinase inhibitor, remains a key challenge in the treatment of EGFR-mutated non-small cell lung cancer (NSCLC). Although retreatment with earlier-generation EGFR tyrosine kinase inhibitors has been studied, data on osimertinib rechallenge are limited. We conducted a single institution retrospective analysis of patients with EGFR-mutated NSCLC who were rechallenged with osimertinib following progression on prior osimertinib and interim systemic therapy, including chemotherapy. Seventeen patients met inclusion criteria, all with adenocarcinoma histology and either EGFR exon 19 deletions or L858R mutations. Median interval between osimertinib treatments was 10.5 months. Osimertinib retreatment resulted in a partial response in 18 % (3/17) and stable disease in 35 % of patients (6/17), for a disease control rate of 53 % (9/17). Median retreatment duration was 4.3 months, and median overall survival following retreatment initiation was 8.9 months. Among patients with central nervous system involvement, several experienced intracranial stability without additional radiation. Duration of initial osimertinib therapy did not strongly predict retreatment benefit. These findings suggest that osimertinib rechallenge may provide clinically meaningful disease control in a subset of patients, especially given its tolerability and oral formulation. Further research is needed to identify biomarkers of sensitivity and to optimize patient selection for osimertinib retreatment following interval chemotherapy.

Indexed as

AcrylamidesAniline CompoundsCarcinoma, Non-Small-Cell LungLung NeoplasmsProtein Kinase InhibitorsAdultAgedAged, 80 and overErbB ReceptorsFemaleHumansIndolesMaleMiddle AgedMutationPyrimidinesAcrylamidesAniline CompoundsEGFR protein, humanErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidinesLung cancerOsimertinibRechallengeRetreatmentTargeted therapy

Identifiers

PMID41175446
PMCPMC12758605

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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.