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ArticleStrahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]2025

Myxoid liposarcoma: treatment outcomes, metastatic pattern and volumetric analysis.

Vlatko Potkrajcic, Merle Zschiegner, Maximilian Niyazi, Verena Warm, Johannes Tobias Thiel, Sandra Frantz, Christoph K W Deinzer, Franziska Szelat, Elgin Hoffmann, Frank Paulsen and 1 more

Abstract read
In one paragraph

Article in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 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
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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

11 authors.

Vlatko PotkrajcicDepartment of Radiation Oncology, University Hospital Tübingen, Eberhard-Karls-University of Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany. vlatko.potkrajcic@med.uni-tuebingen.de.ORCID 0000-0003-4393-413X
Merle ZschiegnerDepartment of Radiation Oncology, University Hospital Tübingen, Eberhard-Karls-University of Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.
Maximilian NiyaziDepartment of Radiation Oncology, University Hospital Tübingen, Eberhard-Karls-University of Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.
Verena WarmDepartment of General and Molecular Pathology and Pathologic Anatomy, University Hospital Tübingen, Liebermeisterstraße 8, 72076, Tuebingen, Germany.
Johannes Tobias ThielDepartment of Hand, Plastic, Reconstructive and Burn Surgery, BG Unfallklinik, Schnarrenbergstraße 95, 72076, Tuebingen, Germany.
Sandra FrantzDepartment of Orthopaedic Surgery, University Hospital Tübingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.
Christoph K W DeinzerDepartment of Medical Oncology and Pneumology, Medical University Hospital Tuebingen, Otfried-Mueller-Straße 10, 72076, Tuebingen, Germany.
Franziska SzelatDepartment of Radiation Oncology, University Hospital Tübingen, Eberhard-Karls-University of Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.
Elgin HoffmannDepartment of Radiation Oncology, University Hospital Tübingen, Eberhard-Karls-University of Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.
Frank PaulsenDepartment of Radiation Oncology, University Hospital Tübingen, Eberhard-Karls-University of Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.
Franziska EckertDepartment of Radiation Oncology, University Hospital Tübingen, Eberhard-Karls-University of Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyxoid liposarcoma (MLPS) is a rare subtype of soft tissue sarcoma. This entity has a specific clinical behavior, characterized with a distinct pattern of hematogenous spread, as well as with a unique radiosensitivity and chemosensitivity. Oncologic results, metastatic patterns and treatment response after multimodal therapy were evaluated in a unicentric patient cohort.

methodsPatients with myxoid liposarcoma were retrospectively analyzed in a single institution analysis (n = 31). Oncologic outcomes were evaluated in 28 patients with localized MLPS treated with multimodal therapy in curative intent. Metastatic pattern was analyzed in additional 3 patients with initially metastatic disease. In patients treated with concomitant MR-guided hyperthermia in the preoperative setting (n = 7), tumor size response was evaluated longitudinally during radio(-chemo)therapy in thermometry MRIs and before surgery (based on preoperative imaging).

resultsThe median follow-up was 4.1 ± 1.0 years. The most common anatomic localization was the lower extremity (78.6%). The 5‑year rates for oncologic outcomes in 28 patients treated in curative intent were 91.7% (± 8.0%) for overall survival (OS), 77.4% (± 11.0%) for local control (LC), 60.1% (± 10.6%) for distant metastasis-free survival (DMFS) and 55.4% (± 11.1%) for disease free survival (DFS). Excellent 5‑year LC (94.7 ± 5.1%) was demonstrated for the cohort excluding 5 patients treated for local recurrences. Most patients had good pathologic response (< 10% vital tumor tissue) following neoadjuvant treatment (82.4%, 14/17). However, this did not correlate with oncologic outcomes. A specific pattern of distant metastases has been observed, with predilection for soft tissues as the most common metastatic site. Furthermore, no isolated pulmonary metastases were observed. The MR analysis demonstrated a significant tumor size reduction (≥ 25%) of the initial tumor volume in 85.7% (n = 6/7) patients. No local recurrences and no distant metastases were observed in patients with significant MR size reduction.

conclusionSequential MRIs during preoperative radiotherapy of myxoid liposarcoma show distinct patterns of the known size reduction of this specific subentity. Our analysis of metastatic patterns demonstrate mostly soft tissue metastases, no patient experienced isolated pulmonary metastases.

Indexed as

Liposarcoma, MyxoidSoft Tissue NeoplasmsAdultAgedCombined Modality TherapyFemaleHumansHyperthermia, InducedMagnetic Resonance ImagingMaleMiddle AgedRetrospective StudiesSurvival RateTreatment OutcomeTumor BurdenHyperthermiaMetastatic patternMyxoid liposarcomaSoft tissue sarcoma

Identifiers

PMID39900817
PMCPMC12700943

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