Evidence map›Paper›PMID 35552929›Full record

ArticleAnnals of surgical oncology2022

Prognostic Factors for Leiomyosarcoma with Isolated Metastases to the Lungs: Impact of Metastasectomy.

Theresa Stork, Balazs Hegedüs, Wiebke Guder, Rainer Hamacher, Jendrik Hardes, Moritz Kaths, Till Plönes, Christoph Pöttgen, Hans-Ulrich Schildhaus, Arne Streitbürger and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of surgical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Theresa StorkDepartment of Thoracic Surgery, Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
Balazs HegedüsDepartment of Thoracic Surgery, Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
Wiebke GuderGerman Cancer Consortium (DKTK), Center Essen, Germany.
Rainer HamacherGerman Cancer Consortium (DKTK), Center Essen, Germany.
Jendrik HardesGerman Cancer Consortium (DKTK), Center Essen, Germany.
Moritz KathsGerman Cancer Consortium (DKTK), Center Essen, Germany.
Till PlönesDepartment of Thoracic Surgery, Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
Christoph PöttgenGerman Cancer Consortium (DKTK), Center Essen, Germany.
Hans-Ulrich SchildhausGerman Cancer Consortium (DKTK), Center Essen, Germany.
Arne StreitbürgerGerman Cancer Consortium (DKTK), Center Essen, Germany.
Juergen TreckmannGerman Cancer Consortium (DKTK), Center Essen, Germany.
Sebastian BauerGerman Cancer Consortium (DKTK), Center Essen, Germany.
Clemens Aigner *Department of Thoracic Surgery, Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany. clemens.aigner@rlk.uk-essen.de.ORCID http://orcid.org/0000-0002-7787-991X
Stéphane Collaud *Department of Thoracic Surgery, Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
Deutschen Konsortium für Translationale Krebsforschung · DERuhrlandklinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeiomyosarcoma (LMS) most frequently metastasizes to the lung. Metastatic LMS is considered incurable. Selected patients may benefit from pulmonary metastasectomy (PM) within multimodal therapy. This study analyzed the prognostic relevance of clinicopathologic factors in these patients.

methodsPatients with metastatic LMS to the lung treated in our center from 2004 to 2020 were included in this single-center retrospective study. Overall survival (OS), progression-free survival (PFS), and prognostic factors were analyzed.

resultsThe study had 64 patients (33 males, 52%) with metastatic LMS to the lung. The 5-year OS was 55% after the diagnosis of pulmonary metastases. Age older than 60 years at the primary tumor diagnosis, primary tumor larger than 70 mm, and five or more lung metastases were associated with poorer OS. Of the 64 patients, 44 underwent PM. The postoperative mortality rate was 0%. The patients selected for PM were younger and had smaller primary tumors, fewer metastases, and metastases that more often were metachronous. Metastasis grade (G1 vs. G2/3) and size (20-mm cutoff) were significant prognostic factors for OS (p = 0.05) and PFS (p = 0.028) after PM, respectively. The 44 patients who underwent PM had a survival benefit compared with the patients who were selected but did not undergo PM (n = 6) and the patients who were not selected for PM (n = 14). Three patients (7%) were alive and free of disease at the last follow-up visit respectively 5.5, 9, and 12 years after PM.

conclusionsFor patients with leiomyosarcoma, PM is safe. Despite aggressive multimodal treatment, most patients will experience recurrence and eventually die of their disease. However, a small subgroup of patients could potentially be cured after PM.

Identifiers

PMID35552929
PMCPMC9174305
OpenAlexW4280558778

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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.