Evidence map›Paper›PMID 39971592›Full record

ArticleBMJ open quality2025

Reduced wait times for molecular-biomarker testing among patients with advanced lung cancer using parallel sample processing and closed-loop communication: the Continuous Oncopanel and ALK Status Tracking (COAST) Project.

Sarah Yeo, Jane Sun, Kelly Zibrik, Tawimas Shaipanich, Hannah Carolan, Barbara Melosky, Diana Ionescu, Deepu Alex, Stephen Yip, Ying Wang

Abstract read
In one paragraph

Article in BMJ open quality, 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. Article
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

10 authors.

Sarah YeoThe University of British Columbia, Vancouver, British Columbia, Canada.ORCID http://orcid.org/0009-0008-1455-8167
Jane SunBC Cancer-Vancouver, Vancouver, British Columbia, Canada.
Kelly ZibrikBC Cancer-Vancouver, Vancouver, British Columbia, Canada.
Tawimas ShaipanichDivision of Respiratory Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.
Hannah CarolanRadiation Oncology, BC Cancer-Vancouver, Vancouver, British Columbia, Canada.
Barbara MeloskyThe University of British Columbia, Vancouver, British Columbia, Canada.
Diana IonescuDepartment of Pathology, BC Cancer-Vancouver, Vancouver, British Columbia, Canada.
Deepu AlexDepartment of Pathology, BC Cancer-Vancouver, Vancouver, British Columbia, Canada.
Stephen YipDepartment of Pathology, BC Cancer-Vancouver, Vancouver, British Columbia, Canada.
Ying WangThe University of British Columbia, Vancouver, British Columbia, Canada Ying.Wang@bccancer.bc.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGiven how crucial molecular-biomarker testing is to treatment decisions for advanced non-small cell lung cancer (NSCLC), guidelines recommend a turnaround time (TAT) of 14 calendar days from receiving specimen to test result, and 3 days to receive a specimen from outside pathology lab. Current TAT for molecular-biomarker testing in British Columbia (BC), Canada frequently exceeds these recommendations. Thus, we launched a quality improvement (QI) initiative to improve TAT of molecular-biomarker testing.

methodsWe assembled a multidisciplinary team to identify areas contributing to delays in molecular-biomarker testing. We designed and conducted three Plan-Do-Study-Act (PDSA) cycles. Cycles 1 and 2 involved changing requisition delivery method from fax to email between BC Cancer Vancouver Centre (BCCV) and two outside hospitals with the highest volume of specimens. Cycle 3 introduced parallel processing of specimens at BCCV pathology lab and concurrent molecular-biomarker testing. TAT was evaluated before and after these process changes along with staff satisfaction via survey.

resultsThe average TAT from test request to specimen received by BCCV was reduced from 6.4 days prechange to 4.6 days postchange. The TAT from specimen receipt by BCCV to report availability was reduced from a median of 22-16 days. Report availability for initial medical oncology consultation increased from a median of 13%-29%. The staff satisfaction survey revealed an enhanced experience with the new process, particularly for our nurse navigator.

conclusionThe TAT for molecular-biomarker testing is an ongoing and complex challenge for healthcare systems worldwide. This QI project is a step towards addressing province-wide reduction in wait times for molecular-biomarker testing results in BC. We continue to explore further ideas to improve workflow metrics and patient care among patients with advanced NSCLC.

Indexed as

Lung NeoplasmsSpecimen HandlingWaiting ListsAnaplastic Lymphoma KinaseBiomarkers, TumorBritish ColumbiaCarcinoma, Non-Small-Cell LungHumansQuality ImprovementSurveys and QuestionnairesTime FactorsALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorContinuous quality improvementHealthcare quality improvementPDSA

Identifiers

PMID39971592
PMCPMC11840910

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.