Evidence map›Paper›PMID 39057174›Full record

ArticleCurrent oncology (Toronto, Ont.)2024

Confirmation of Recurrent Lung Cancer Following Resection Using Liquid Biopsy, a Proof-of-Concept Real-World Study.

Julia R Naso, Stephen Yip, Curtis Hughesman, Barb Melosky, Tanner Dowhy, Melissa K McConechy, John C English, Penelope M A Brasher, James Choi, Kyle Grant and 3 more

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

13 authors.

Julia R NasoDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC V5Z 4E6, Canada.
Stephen YipDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC V5Z 4E6, Canada.ORCID 0000-0002-8514-9861
Curtis HughesmanDepartment of Pathology, BC Cancer, Vancouver, BC V5Z 4E6, Canada.
Barb MeloskyDepartment of Medical Oncology, BC Cancer, Vancouver, BC V5Z 4E6, Canada.ORCID 0000-0003-2865-659X
Tanner DowhyCanada's Michael Smith Genome Sciences Centre, Vancouver, BC V5Z 4S6, Canada.
Melissa K McConechyCanada's Michael Smith Genome Sciences Centre, Vancouver, BC V5Z 4S6, Canada.
John C EnglishDepartment of Pathology and Laboratory Medicine, Vancouver General Hospital, Vancouver, BC V5Z 1M9, Canada.ORCID 0000-0002-7442-9147
Penelope M A BrasherCentre for Clinical Epidemiology and Evaluation, Vancouver Coastal Health Research Institute, Vancouver, BC V5Z 1M9, Canada.
James ChoiDivision of Thoracic Surgery, Department of Surgery, Vancouver General Hospital, Vancouver, BC V5Z 1M9, Canada.ORCID 0000-0002-6988-8648
Kyle GrantDivision of Thoracic Surgery, Department of Surgery, Vancouver General Hospital, Vancouver, BC V5Z 1M9, Canada.
John YeeDivision of Thoracic Surgery, Department of Surgery, Vancouver General Hospital, Vancouver, BC V5Z 1M9, Canada.
Stephen LamDivision of Respirology, Department of Medicine, BC Cancer, Vancouver, BC V5Z 4E6, Canada.
Anna McGuireDivision of Thoracic Surgery, Department of Surgery, Vancouver General Hospital, Vancouver, BC V5Z 1M9, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Appropriate management requires timely and accurate confirmation of non-small cell lung cancer (NSCLC) recurrence in patients who have had curative-intent surgical resection. We assessed the association between circulating tumor DNA (ctDNA) identified using amplicon sequencing and evidence of recurrence on CT surveillance. A prospective cohort study of NSCLC patients with early-stage disease undergoing curative-intent resection was conducted. Surveillance was performed post-operatively at pre-defined intervals with both liquid biopsy and chest CT imaging. Amplicon panel next-generation sequencing was performed on DNA and RNA from tumor tissue and on plasma cell-free DNA for tumor-informed ctDNA detection. Resected tumors from 78 NSCLC patients were analyzed. Alterations were detected on the DNA assay for 65 tumors and only on the RNA assay for 4 tumors. Of the 65 patients with alterations detected on the tumor DNA assay, 29 completed post-operative liquid biopsy testing. Four of those 29 patients had evidence of recurrence on imaging, of whom two had biopsy confirmation of recurrence and detectable ctDNA at the 12-month follow-up. Molecular confirmation of NSCLC recurrence can be provided through amplicon sequencing of plasma cell-free DNA in cases with imaging evidence of recurrence. Invasive tissue diagnosis may be avoidable in patients with ctDNA confirmation of recurrence that is suspected based on imaging. Further study of ctDNA assessment technologies in the setting of suspected recurrence is necessary to inform post-operative lung cancer surveillance guidelines.

Indexed as

Carcinoma, Non-Small-Cell LungCirculating Tumor DNALung NeoplasmsNeoplasm Recurrence, LocalAgedAged, 80 and overFemaleHumansLiquid BiopsyMaleMiddle AgedProspective StudiesCirculating Tumor DNAbiomarkerlung cancernext-generation sequencingtargeted therapy

Identifiers

PMID39057174
PMCPMC11276127

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.