Evidence map›Paper›PMID 36865932›Full record

ReviewBreathe (Sheffield, England)2022

Idiopathic pulmonary fibrosis and lung cancer: future directions and challenges.

Ahmad Abu Qubo, Jamil Numan, Juan Snijder, Maria Padilla, John H M Austin, Kathleen M Capaccione, Monica Pernia, Jean Bustamante, Timothy O'Connor, Mary M Salvatore

Open access · diamondAbstract readReview
In one paragraph

Review in Breathe (Sheffield, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
7.1field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Lung cancer risk and occupational pulmonary fibrosis: systematic review and meta-analysis.European respiratory review : an official journal of the European Respiratory Society · 2024
    Pooled it
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  13. Long non-coding RNAMolecular therapy. Nucleic acids · 2025
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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

10 authors at 5 institutions in 2 countries.

Ahmad Abu QuboDepartment of Pathology, Faculty of Medicine, Hashemite University, Zarqa, Jordan.ORCID https://orcid.org/0000-0001-8584-2407
Jamil NumanDepartment of Radiology, Columbia University Medical Center, New York, NY, USA.
Juan SnijderDepartment of Pediatrics, Einstein Medical Center, Philadelphia, PA, USA.
Maria PadillaDepartment of Pulmonary Medicine, Mount Sinai, New York, NY, USA.
John H M AustinDepartment of Radiology, Columbia University Medical Center, New York, NY, USA.
Kathleen M CapaccioneDepartment of Radiology, Columbia University Medical Center, New York, NY, USA.ORCID https://orcid.org/0000-0002-6536-2673
Monica PerniaDepartment of Medicine, Metropolitan Hospital, New York, NY, USA.
Jean BustamanteDepartment of Oncology, West Virginia University, Morgantown, WV, USA.
Timothy O'ConnorDepartment of Radiology, Columbia University Medical Center, New York, NY, USA.
Mary M SalvatoreDepartment of Radiology, Columbia University Medical Center, New York, NY, USA.
Columbia University Irving Medical Center · USEinstein Medical Center Philadelphia · USHashemite University · JOMetropolitan Hospital Center · USWest Virginia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive disease of pulmonary scarring. New treatments slow disease progression and allow pulmonary fibrosis patients to live longer. Persistent pulmonary fibrosis increases a patient's risk of developing lung cancer. Lung cancer in patients with IPF differs from cancers that develop in the non-fibrotic lung. Peripherally located adenocarcinoma is the most frequent cell type in smokers who develop lung cancer, while squamous cell carcinoma is the most frequent in pulmonary fibrosis. Increased fibroblast foci in IPF are associated with more aggressive cancer behaviour and shorter doubling times. Treatment of lung cancer in fibrosis is challenging because of the risk of inducing an exacerbation of fibrosis. In order to improve patient outcomes, modifications of current lung cancer screening guidelines in patients with pulmonary fibrosis will be necessary to avoid delays in treatment. 2-fluoro-2-deoxy-d-glucose (FDG) positron emission tomography (PET) computed tomography (CT) imaging can help identify cancer earlier and more reliably than CT alone. Increased use of wedge resections, proton therapy and immunotherapy may increase survival by decreasing the risk of exacerbation, but further research will be necessary.

Identifiers

PMID36865932
PMCPMC9973524
OpenAlexW4313907232

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.