Evidence map›Paper›PMID 36650544›Full record

ReviewRespiratory research2023

Optimizing molecular testing of lung cancer needle biopsy specimens: potential solutions from an interdisciplinary qualitative study.

Florian J Fintelmann, Nikki A Martin, Ismail Tahir, Elissa M Quinn, Timothy C Allen, Lija Joseph, Boris Nikolic, Christopher Lee

Open access · goldAbstract readReview
In one paragraph

Review in Respiratory research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 7 institutions in 1 country.

Florian J FintelmannDepartment of Radiology, Division of Thoracic Imaging and Intervention, Massachusetts General Hospital, 55 Fruit Street, Boston, MA, 02114, USA. fintelmann@mgh.harvard.edu.
Nikki A MartinLUNGevity Foundation, Bethesda, MD, USA.
Ismail TahirDepartment of Radiology, Division of Thoracic Imaging and Intervention, Massachusetts General Hospital, 55 Fruit Street, Boston, MA, 02114, USA.
Elissa M QuinnBlueprint Medicines, Boston, MA, USA.
Timothy C AllenBeaumont Hospital, Royal Oak, MI, USA.
Lija JosephLowell General Hospital, Lowell, MA, USA.
Boris NikolicWyoming Valley Radiology Associates, Wilkes-Barre General Hospital, Wilkes-Barre, PA, USA.
Christopher LeeDepartment of Imaging, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Massachusetts General Hospital · USBeaumont Hospital, Royal Oak · USBlueprint Medicines (United States) · USCedars-Sinai Medical Center · USCommunity Health Systems - Wilkes-Barre General Hospital · USLowell General Hospital · USLUNGevity Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMolecular testing can detect actionable genomic alterations and tumor cell surface proteins in patients with non-small cell lung cancer (NSCLC). However, utilization remains suboptimal, representing missed treatment opportunities. This study aimed to identify challenges and potential solutions to obtaining percutaneous lung needle biopsy specimens for successful molecular testing in patients with advanced NSCLC.

methodsThis interdisciplinary qualitative study included ten radiologists and four pathologists from academic and community settings across the United States who routinely perform and analyze percutaneous lung needle biopsies. Participants underwent semi-structured one-on-one interviews (Phase 1). Interview questionnaires were constructed based on a literature review of key lines of inquiry and conducted by professional market researchers using the theoretical domains framework. Primary barriers to molecular testing were identified using thematic analysis. Subsequently, multidisciplinary focus groups were convened to identify potential solutions (Phase 2).

resultsFour themes emerged as barriers to molecular testing and were matched to the clinical workflow: (1) biopsy request, (2) biopsy procedure, (3) specimen analysis, and (4) communication. The nineteen potential solutions included adding a "checkbox" to indicate molecular testing in the biopsy request, leveraging pre-procedural imaging to guide biopsies, conserving tissue through appropriate allocation strategies and next generation sequencing panels instead of sequential single-gene assays, instituting reflex-molecular testing upon NSCLC diagnosis, tracking and communicating biopsy outcomes at multidisciplinary tumor boards, and improving integration of radiologists and pathologists into oncology care teams.

conclusionsPotential solutions exist to increase successful molecular testing of lung needle biopsy specimens in patients with advanced NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsBiopsyBiopsy, NeedleHumansMolecular Diagnostic TechniquesUnited StatesBiomarker testingGenomic analysisLung cancerLung needle biopsyMolecular analysis

Identifiers

PMID36650544
PMCPMC9847026
OpenAlexW4316814824

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.