Evidence map›Paper›PMID 40940895›Full record

ArticleCancers2025

Oligometastatic Mesothelioma Treated with Ablative Radiotherapy (OMAR): A Multicenter Study.

Davide Franceschini, Paolo Ghirardelli, Patricia Frrokaj, Nicolaus H Andratschke, Luca Nicosia, Elisabetta Parisi, Gaia Piperno, Matteo Sepulcri, Emanuele Alì, Antonio Marco Marzo and 13 more

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Davide FranceschiniDepartment of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy.ORCID 0000-0003-1142-2439
Paolo GhirardelliDepartment of Radiotherapy, Cliniche Humanitas Gavazzeni, via Gavazzeni 21, 24125 Bergamo, Italy.
Patricia FrrokajDepartment of Radiation Oncology, University Hospital Zurich, University of Zurich, Rämistrasse 100, 8091 Zurich, Switzerland.
Nicolaus H AndratschkeDepartment of Radiation Oncology, University Hospital Zurich, University of Zurich, Rämistrasse 100, 8091 Zurich, Switzerland.
Luca NicosiaAdvanced Radiation Oncology Department, IRCCS Sacro Cuore Don Calabria Hospital, Cancer Care Center, 37034 Negrar Di Valpolicella, Italy.ORCID 0000-0002-0731-8041
Elisabetta ParisiIRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", 47014 Meldola, Italy.
Gaia PipernoDivision of Radiotherapy, IEO European Institute of Oncology IRCCS, 20141 Milan, Italy.ORCID 0000-0002-5358-1297
Matteo SepulcriRadiation Therapy Unit, Veneto Institute of Oncology IOV-IRCCS, 35128 Padova, Italy.ORCID 0000-0002-9654-5587
Emanuele AlìRadiation Oncology Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Antonio Marco MarzoDepartment of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy.ORCID 0000-0002-2549-4583
Stefano BendoniDepartment of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy.
Ruggero SpotoDepartment of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy.
Marco KrengliDipartimento di Scienze Chirurgiche, Oncologiche e Gastroenterologiche, Università di Padova e Istituto Oncologico Veneto-IRCCS, 35128 Padova, Italy.ORCID 0000-0002-2064-8379
Patrizia CiammellaRadiation Oncology Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Barbara A Jereczek-FossaDivision of Radiotherapy, IEO European Institute of Oncology IRCCS, 20141 Milan, Italy.ORCID 0000-0001-8151-3673
Antonino RomeoIRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", 47014 Meldola, Italy.
Rosario MazzolaDepartment of Radiotherapy, Cliniche Humanitas Gavazzeni, via Gavazzeni 21, 24125 Bergamo, Italy.
Filippo AlongiAdvanced Radiation Oncology Department, IRCCS Sacro Cuore Don Calabria Hospital, Cancer Care Center, 37034 Negrar Di Valpolicella, Italy.ORCID 0000-0002-6569-8628
Matthias GuckenbergerDepartment of Radiation Oncology, University Hospital Zurich, University of Zurich, Rämistrasse 100, 8091 Zurich, Switzerland.
Giovanni Luca CeresoliDepartment of Medical Oncology, Cliniche Humanitas Gavazzeni, via Gavazzeni 21, 24125 Bergamo, Italy.ORCID 0000-0001-8599-0629
Mauro LoiDepartment of Radiation Oncology, Azienda Universitaria Ospedaliera Careggi, 50134 Florence, Italy.
Paolo BorghettiRadiation Oncology Department, ASST Spedali Civili and University of Brescia, 25123 Brescia, Italy.ORCID 0000-0001-7275-7908
Marta ScorsettiDepartment of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy.ORCID 0000-0003-0320-559X

Funding

Fondazione Oxiamo ONLUS NA
6 · The paper itself

Abstract

BACKGROUND/

objectivesThis multicenter retrospective study aims to evaluate the role of Ablative Radiotherapy (RT) in patients with unresectable pleural mesothelioma (PM) who experienced radiological progression after at least one line of chemotherapy, with a maximum involvement of three pleural or extrapleural sites.

methodsAdult patients (≥18 years) with PM treated with stereotactic radiotherapy between 2011 and 2022, limited to a maximum of three pleural or extrapleural sites, were included in the analysis. Ablative RT was required to be administered with radical intent. Endpoints were time to further systemic therapy (TFST), local control (LC), progression-free survival (PFS), overall survival (OS), and acute and late radiotherapy-related toxicity.

resultsA total of 56 patients were identified from six Italian and one Swiss radiotherapy center. Treatment was generally well tolerated. Ten patients experienced grade 1 or 2 acute toxicity, while four patients reported persistent chest pain, with one case reaching grade 3 as late toxicity. The median TFST was 18.6 months, with TFST rates of 61.7% and 46.4% at 12 and 24 months, respectively. The median OS was 37.63 months, with 1- and 2-year OS rates of 85.2% and 65.6%. Local control was favorable (79% at 1 year), but most patients experienced disease recurrence outside the SABR treatment volume. The median disease progression-free survival (DPFS) was 8.17 months, with 1- and 2-year DPFS rates of 36% and 19%, respectively. Smoking history correlated with OS and DPFS in univariate analysis, while statistical significance for OS was maintained in multivariate analysis. Additionally, nodal status and PTV volume were associated with OS.

conclusionSABR is a safe and effective approach for the treatment of oligorecurrent/oligoprogressive PM. The time to further systemic therapy was extended up to 18 months. At two years, 10% of patients remained disease-free, and more than half were alive at three years, suggesting a potentially indolent biological behavior in oligometastatic PM.

Indexed as

oligometastasesoligorecurrencepleural mesotheliomastereotactic ablative radiation therapy

Identifiers

PMID40940895
PMCPMC12427324

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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.