Evidence map›Paper›PMID 40190818›Full record

ArticleJTO clinical and research reports2025

Brief Report: Real-World Treatment Patterns and Clinical Outcomes for Patients With Advanced ALK-Rearranged NSCLC in British Columbia.

Peiyao Wang, Curtis Hughesman, Stephen Yip, William W Lockwood, Sophie Sun

Abstract read
In one paragraph

Article in JTO clinical and research reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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

5 authors.

Peiyao WangDepartment of Integrative Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.
Curtis HughesmanCancer Genetics and Genomics Laboratory, BC Cancer, Vancouver, British Columbia, Canada.
Stephen YipDepartment of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
William W LockwoodDepartment of Integrative Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.
Sophie SunBritish Columbia Cancer Agency, Vancouver Centre, Vancouver, British Columbia, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: EML4-ALK rearrangements represent an oncogenic driver alteration in 5% of NSCLC cases. We aim to better understand real-world treatment patterns and outcomes of Methods: We performed a retrospective population-based chart review of ALK+ patients with locally advanced or metastatic NSCLC in British Columbia (BC), Canada. Patients diagnosed from January 2014 to May 2023 were identified through the BC Cancer Genetics Laboratory database, and data were collected up to December 2023. Results: A total of 216 patients with stage IIIB, IIIC, or IV ALK+ lung NSCLC were identified. Median age was 60 (range: 24-91) years, 151 (68.9%) had never smoked, and 95 (43.9%) were Asian. The median overall survival was 49.4 months with median follow-up time of 55.4 months. Majority of the cohort (n = 198, 91.7%) received palliative systemic therapy, all of which included at least one ALK tyrosine kinase inhibitor (TKI). The most common first-line regimen was alectinib (n = 97, 49.0%) followed by crizotinib (n = 84, 42.4%); only four and one patient received lorlatinib and brigatinib first line, respectively. Alectinib was frequently prescribed overall, with 80.3% of patients receiving it in any treatment line. Time to treatment discontinuation was significantly longer ( Conclusions: Patients with ALK+ advanced NSCLC in BC have durable responses to ALK TKIs. Despite approval of all ALK TKIs for first-line use since 2021, alectinib is largely the favored agent in BC. Further real-world investigations can refine treatment strategies and shape policies around ALK TKIs for patients with ALK+ NSCLC.

Indexed as

ALKNSCLCReal-worldTargeted therapyTreatment sequencing

Identifiers

PMID40190818
PMCPMC11968262

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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.