Evidence map›Paper›PMID 41522099›Full record

ReviewJournal of thoracic disease2025

Bronchoscopic ablation for non-small cell lung cancer.

Kanishka Rangamuwa, Daniel Steinfort

Abstract readReview
In one paragraph

Review in Journal of thoracic disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

2 authors.

Kanishka RangamuwaDepartment of Respiratory Medicine, Royal Melbourne Hospital, Parkville, Australia.ORCID https://orcid.org/0000-0001-6459-7764
Daniel SteinfortDepartment of Respiratory Medicine, Royal Melbourne Hospital, Parkville, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bronchoscopic ablation is an emerging minimally invasive treatment option for patients with non-small cell lung cancer (NSCLC). Techniques including radiofrequency ablation (RFA), microwave ablation (MWA), pulsed electric field (PEF) ablation, and cryoablation have been evaluated in several feasibility and early clinical studies. These approaches demonstrate technical success with encouraging safety profiles and reduced complication rates compared to percutaneous methods. Bronchoscopic RFA and MWA have shown effective tumour ablation, though isolated mortality events underscore the need for further safety evaluation. PEF ablation has gained attention for its ability to preserve surrounding structures, with early signals of favourable immune activation. Cryoablation, though tested in small cohorts, has demonstrated feasibility with minimal major adverse events. Beyond local control, an emerging theme across modalities is the potential for these treatments to stimulate systemic anti-cancer immunity, with early evidence suggesting enhanced immune responses and possible synergy with immunotherapy. Despite these advances, most studies remain small, with limited follow-up and heterogeneous endpoints, leaving long-term efficacy and optimal technique unresolved. Larger prospective trials are needed to establish safety, durability of tumour control, and comparative outcomes versus established therapies. Nonetheless, the growing body of data highlights bronchoscopic ablation as a developing therapeutic option with the potential to expand lung-sparing treatment strategies and complement evolving immunotherapy paradigms.

Indexed as

ablationBronchoscopynon-small cell lung cancer (NSCLC)thermal ablation

Identifiers

PMID41522099
PMCPMC12780388

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.