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Real-world survival outcomes and adverse events with adjuvant osimertinib in resected EGFR mutation-positive non-small cell lung cancer.

2025· article· en· W4410823208 on OpenAlexaffabout
Vanessa Samuel, Amanda Williams Gibson, Michelle L. Dean, Yaroslav Musiiets, Erik Nohr, Vishal Navani

Bibliographic record

VenueJournal of Clinical Oncology · 2025
Typearticle
Languageen
FieldMedicine
TopicLung Cancer Treatments and Mutations
Canadian institutionsUniversity of CalgaryOccupational Cancer Research Centre
Fundersnot available
KeywordsMedicineOsimertinibAdjuvantOncologyLung cancerInternal medicineAdverse effectMutationCancerLungEpidermal growth factor receptorGeneErlotinibGeneticsBiology

Abstract

fetched live from OpenAlex

e20003 Background: Adjuvant osimertinib (AO) significantly improved disease-free survival and overall survival among patients with resected stage IB to IIIA epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC) in the phase 3 ADAURA trial. A 3-year duration of AO is now guideline recommended. Our study aimed to assess province-wide real-world outcomes of AO for patients with NSCLC harbouring canonical sensitizing EGFR mutations. Methods: A retrospective review was conducted using the Glans-Look Lung Cancer Research database, which captures patient-level demographic, clinical, and outcome data across Alberta, Canada. Patients had resected clinical stage IA-IIIA EGFR exon 19 deletion or L858R mutation and received AO in Alberta between September 2021 - November 2024. EGFR mutation status was obtained using the Agena iPLEX HS Lung panel or Oncomine Focus Assay. Disease-free survival was reported using summary statistics. Date of last follow-up was November 2024. Results: Of the 732 patients with EGFR positive NSCLC diagnosed between 2021 – 2024 in Alberta, 106 patients (14%) had early stage disease (defined as up to IIIA). A total of 25 patients received AO following resection of their NSCLC, with 24 patients (96%) having R0 resections. 11 patients (44%) received adjuvant chemotherapy prior to AO. Median follow up was 12.8 months from initiation of AO. Median duration of AO was 9.8 months (95% CI 6.7 to 16.7 months), with an average dose intensity of 92%. One patient (4%) had disease recurrence following AO, albeit this patient only received 12 days of AO due to toxicity. Disease-free survival ranged from 3.9 – 34.2 months. At the time of analysis, 24 patients (96%) were alive, with one death. Of the 29 adverse events (AE) recorded, there were 13 (45%) grade 1, 13 (45%) grade 2, 1 (3%) grade 4, and 2 (7%) AE of unknown grade. In ADAURA, of the 718 AE reported, there were 493 (69%) grade 1, 202 (28%) grade 2, and 22 (3%) grade 3 AE. Management of adverse events compared to ADAURA is outlined in Table 1. Median time to discontinuation of AO was 2.7 months. Conclusions: AEs occurred less frequently compared to ADAURA, although discontinuation of AO due to AE was higher in our experience, 28% vs. 11%, implying a poorer tolerability of AO in routine practice compared to the trial setting. Similar to ADAURA, most AE were low grade, suggesting that there may be an unmet need for more proactive symptom control to mitigate AE that may lead to discontinuation. Future studies require longer follow-up periods to better describe time to event endpoints for AO in this population. Management of adverse events in the current study compared to the ADAURA clinical trial. Management of Adverse Event Study Patients (n=25) ADAURA Patients (n=337) Dose Modification 4 (16%) 29 (9%) Treatment Break 5 (20%) 80 (24%) Hospitalization or Emergency Room Visit 2 (8%) N/A Discontinued 7 (28%) 37 (11%)

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.071
Threshold uncertainty score0.142

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.002
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.039
GPT teacher head0.475
Teacher spread0.436 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes2
Has abstractyes

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