Evidence map›Paper›PMID 40960505›Full record

ArticleEuropean radiology2026

Outcomes following microwave ablation of 669 primary and metastatic lung malignancies.

Ruben Geevarghese, Erica S Alexander, Ahmed Elsakka, Olivier Chevallier, Luke Kelly, Vlasios S Sotirchos, Constantinos T Sofocleous, Elena N Petre, Joseph P Erinjeri, Chenyang Zhan and 7 more

Abstract read
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In one paragraph

Article in European radiology, 2026. 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
–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

8 citing papers in PubMed.

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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

17 authors.

Ruben GeevargheseDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Erica S AlexanderDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ahmed ElsakkaDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Olivier ChevallierDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Luke KellyDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Vlasios S SotirchosDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Constantinos T SofocleousDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Elena N PetreDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Joseph P ErinjeriDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Chenyang ZhanDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Fourat RidouaniDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Liwei JiangDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Krishna Nand KeshavamurthyDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Robert S SalkinDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Hooman YarmohammadiDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Stephen B SolomonDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Etay ZivDivision of Interventional Radiology, Department of Radiology, Room H118, Memorial Sloan Kettering Cancer Center, New York, NY, USA. zive@mskcc.org.ORCID http://orcid.org/0000-0002-3188-0085

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

objectivesPercutaneous ablation is a treatment modality used in the management of primary and metastatic lung malignancies. Factors affecting local control rate (LCR) following microwave ablation (MWA) are poorly understood due to inconsistent and limited reporting of histology and procedure-related outcomes. MATERIALS AND

methodsSingle-center retrospective study of patients with primary and metastatic lung malignancies who underwent MWA between January 2010 and July 2021. Patient, tumor and ablation characteristics were recorded. Outcomes evaluated included technical success, local tumor control and adverse events (AEs).

resultsA total of 669 nodules were identified from 383 patients (197 male/186 female with a median age of 59 years (IQR = 21 years)) across 459 ablation sessions. This comprised 83 primary and 586 metastatic lung tumors. One-year and two-year local LCRs (±SD) across the cohort were 90.3% (±1.1%) and 84.7% (±1.4%), respectively. Multivariable analysis identified ablation power settings, age, concomitant chemotherapy and histology as significant covariates associated with time to local recurrence (TTLR). Standard power was associated with longer TTLR, compared to low power, with no significant difference in AE rates. A significant difference in TTLR was noted between different histological groups.

conclusionMWA of primary and metastatic lung tumors is safe and effective. LCRs differ across different histologies. Standard power MWA is associated with longer TTLR without increased AEs rates. KEY POINTS: Question Reported local control rates for microwave ablation (MWA) vary widely, with limited and heterogeneous data on histology-specific and parameter-related outcomes, leaving a gap in understanding. Findings MWA achieved 90.3% and 84.7% one- and two-year local control rates, with longer time to recurrence for standard power MWA. Histology-specific differences noted in time to recurrence. Clinical relevance MWA is a safe and effective treatment for primary and secondary lung cancers, offering comparable local control rates to radiotherapy and surgical resection. Further refinement of treatment parameters may enhance outcomes and address histology-specific challenges.

Indexed as

Ablation TechniquesLung NeoplasmsMicrowavesAdultAgedFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalRetrospective StudiesTreatment OutcomeAblationLung cancerMetastaticMicrowaveNSCLC

Identifiers

What OpenQuestion holds

Textmetadata
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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.