Evidence map›Paper›PMID 39319506›Full record

ArticleInternational journal of cancer2025

Oligometastatic non-small cell lung cancer: Impact of local and contemporary systemic treatment approaches on clinical outcome.

Marcel Wiesweg, Claudia Küter, Johannes Schnorbach, Julius Keyl, Martin Metzenmacher, Jelena Cvetkovic, Felix Carl Saalfeld, Franziska Glanemann, Wilfried Eberhardt, Filiz Oezkan and 14 more

Abstract readMulticenter Study
In one paragraph

Article in International journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
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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

24 authors.

Marcel WieswegDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.ORCID 0000-0002-9698-9559
Claudia KüterDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Johannes SchnorbachDepartment of Thoracic Oncology, Thoraxklinik, Heidelberg University Hospital, Heidelberg, Germany.
Julius KeylInstitute of Pathology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Martin MetzenmacherDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Jelena CvetkovicDepartment of Thoracic Oncology, Thoraxklinik, Heidelberg University Hospital, Heidelberg, Germany.
Felix Carl SaalfeldClinic for Internal Medicine I, University Hospital, Technische Universität Dresden, Dresden, Germany.
Franziska GlanemannDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Wilfried EberhardtDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.ORCID 0000-0003-4284-3586
Filiz OezkanDepartment of Pulmonary Medicine, Section of Interventional Pneumology, West German Cancer Center, University Medicine Essen-Ruhrlandklinik, University Duisburg-Essen, Essen, Germany.
Dirk TheegartenInstitute of Pathology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Albrecht StenzingerInstitute of Pathology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.ORCID 0000-0003-1001-103X
Kaid DarwicheDepartment of Pulmonary Medicine, Section of Interventional Pneumology, West German Cancer Center, University Medicine Essen-Ruhrlandklinik, University Duisburg-Essen, Essen, Germany.
Dirk KoschelDepartment of Pneumology, Fachkrankenhaus Coswig, Lung Center, Coswig and Division of Pneumology, Medical Department I, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Felix HerthDepartment of Pneumology and Critical Care Medicine, Heidelberg University Hospital, Heidelberg University, Heidelberg, Germany.
Servet BölükbasNational Center for Tumor Diseases (NCT), NCT West, Essen, Germany.
Hauke WinterNational Center for Tumor Diseases (NCT), NCT Heidelberg, a partnership between DKFZ and Heidelberg University Hospital, Heidelberg, Germany.
Fabian WeykampDepartment of Radiation Oncology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
Martin WermkeClinic for Internal Medicine I, University Hospital, Technische Universität Dresden, Dresden, Germany.
Martin StuschkeNational Center for Tumor Diseases (NCT), NCT West, Essen, Germany.
Till PlönesNational Center for Tumor Diseases (NCT/UCC), Dresden, and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Michael ThomasDepartment of Thoracic Oncology, Thoraxklinik, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-9511-055X
Martin SchulerDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Petros ChristopoulosDepartment of Thoracic Oncology, Thoraxklinik, Heidelberg University Hospital, Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oligometastatic (OMD) non-small cell lung cancer (NSCLC) is a distinct but heterogeneous entity. Current guidelines recommend systemic therapy and consolidation with local ablative therapy (LAT). However, evidence regarding the optimal choice of multimodal treatment approaches is lacking, in particular with respect to the integration of immunotherapy. This real-world study identified 218 patients with OMD NSCLC (2004-2023, prespecified criteria: ≤5 metastases in ≤2 organ systems) from three major German comprehensive cancer centers. Most patients had one (72.5%) or two (17.4%) metastatic lesions in a single (89.9%) organ system. Overall survival (OS) was significantly longer with a single metastatic lesion (HR 0.54, p = .003), and female gender (HR 0.4, p < .001). Median OS of the full cohort was 27.8 months, with 29% survival at 5 years. Patients who had completed LAT to all NSCLC sites, typically excluding patients with early progression, had a median OS of 34.4 months (37.7% 5-year OS rate) with a median recurrence-free survival (RFS) of 10.9 months (13.3% at 5 years). In those patients, systemic treatment as part of first-line therapy was associated with doubling of RFS (12.3 vs. 6.4 months, p < .001). Despite limited follow-up of patients receiving chemo-immunotherapy (EU approval 2018/2019), RFS was greatly improved by adding checkpoint inhibitors to chemotherapy (HR 0.44, p = .008, 2-year RFS 51.4% vs. 15.1%). In conclusion, patients with OMD NSCLC benefitted from multimodality approaches integrating systemic therapy and local ablation of all cancer sites. A substantial proportion of patients achieved extended OS, suggesting a potential for cure that can be further augmented with the addition of immunotherapy.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAdultAgedAged, 80 and overCombined Modality TherapyFemaleHumansImmunotherapyMaleMiddle AgedNeoplasm MetastasisRetrospective StudiesTreatment Outcomeimmunotherapylocally ablative treatmentmultimodal conceptsobservational studyoligometastatic NSCLC

Identifiers

PMID39319506
PMCPMC11661509

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Registered trials

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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.