Intermuscular extremity myxoid liposarcoma can be managed by marginal resection following neoadjuvant radiotherapy.


Journal

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
ISSN: 1532-2157
Titre abrégé: Eur J Surg Oncol
Pays: England
ID NLM: 8504356

Informations de publication

Date de publication:
02 2023
Historique:
received: 25 07 2022
revised: 10 09 2022
accepted: 12 09 2022
pubmed: 16 10 2022
medline: 3 3 2023
entrez: 15 10 2022
Statut: ppublish

Résumé

Compared with other soft tissue sarcomas, myxoid liposarcoma (MLS) occurs in younger patients, has a propensity for intermuscular locations and is highly radiosensitive. With pre-operative radiotherapy, intermuscular MLS demonstrates substantial volume reduction and can be easily separated from surrounding tissues during resection. However, it is unclear whether marginal excision of MLS is oncologically safe. This study aimed to assess the association between margins and survival in irradiated, intermuscular MLS. The study identified 198 patients from seven sarcoma centres with a first presentation of localized, extremity, intermuscular MLS that received pre-operative radiotherapy and was diagnosed between 1990 and 2017. Patient and treatment characteristics, radiological and histological responses to neoadjuvant treatment and clinical surveillance were recorded. Margins were microscopically positive in 11% (n = 22), <1.0 mm in 15% (n = 29) and ≥1.0 mm in 72% (n = 143). There was no association between margin status and local recurrence-free, metastasis-free or overall survival. This finding held true even in patients at higher risk of worse overall survival based on multivariable analysis (% round cell≥5%, percentage ellipsoid tumour volume change ≤ -60.1%). Irradiated, extremity, intermuscular myxoid liposarcoma can safely undergo marginal resection without compromising oncologic control.

Sections du résumé

BACKGROUND
Compared with other soft tissue sarcomas, myxoid liposarcoma (MLS) occurs in younger patients, has a propensity for intermuscular locations and is highly radiosensitive. With pre-operative radiotherapy, intermuscular MLS demonstrates substantial volume reduction and can be easily separated from surrounding tissues during resection. However, it is unclear whether marginal excision of MLS is oncologically safe. This study aimed to assess the association between margins and survival in irradiated, intermuscular MLS.
METHODS
The study identified 198 patients from seven sarcoma centres with a first presentation of localized, extremity, intermuscular MLS that received pre-operative radiotherapy and was diagnosed between 1990 and 2017. Patient and treatment characteristics, radiological and histological responses to neoadjuvant treatment and clinical surveillance were recorded.
RESULTS
Margins were microscopically positive in 11% (n = 22), <1.0 mm in 15% (n = 29) and ≥1.0 mm in 72% (n = 143). There was no association between margin status and local recurrence-free, metastasis-free or overall survival. This finding held true even in patients at higher risk of worse overall survival based on multivariable analysis (% round cell≥5%, percentage ellipsoid tumour volume change ≤ -60.1%).
CONCLUSION
Irradiated, extremity, intermuscular myxoid liposarcoma can safely undergo marginal resection without compromising oncologic control.

Identifiants

pubmed: 36243649
pii: S0748-7983(22)00659-X
doi: 10.1016/j.ejso.2022.09.008
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

362-367

Informations de copyright

Copyright © 2022. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Jonathan R Perera (JR)

Orthopaedic Oncology, Royal National Orthopaedic Hospital, London, United Kingdom. Electronic address: Jonathan.Perera@nhs.net.

Meshal AlFaraidy (M)

University Musculoskeletal Oncology Unit, Sinai Health System, Division of Orthopaedic Surgery, Department of Surgery, University of Toronto, Toronto, ON, Canada.

Izuchukwu Ibe (I)

Orthopaedic Oncology, University of Mississippi Medical Center, USA.

Ahmed Aoude (A)

Orthopaedic Oncology, McGill University, Montreal, QC, Canada.

Ibtissam Acem (I)

Surgical Oncology and Gastrointestinal Surgery Erasmus MC Cancer Institute, Rotterdam, the Netherlands; Orthopaedic Oncology Leiden University Medical Centre, Leiden, the Netherlands.

Michiel A J van de Sande (MAJ)

Orthopaedic Oncology Leiden University Medical Centre, Leiden, the Netherlands.

Mireille Dessureault (M)

Orthopaedic Oncology, McGill University, Montreal, QC, Canada.

Robert E Turcotte (RE)

Orthopaedic Oncology, McGill University, Montreal, QC, Canada.

Sophie Mottard (S)

Orthopaedic Oncology Université de Montreal, Montreal, QC, Canada.

Georges Basile (G)

Orthopaedic Oncology Université de Montreal, Montreal, QC, Canada.

Marc Isler (M)

Orthopaedic Oncology Université de Montreal, Montreal, QC, Canada.

Hugo Saint-Yves (H)

Orthopaedic Oncology Université de Montreal, Montreal, QC, Canada.

Nicholas Eastley (N)

Orthopaedic Oncology, Royal Orthopaedic Hospital, Birmingham, United Kingdom.

Jonathan Stevenson (J)

Orthopaedic Oncology, Royal Orthopaedic Hospital, Birmingham, United Kingdom.

Matthew T Houdek (MT)

Orthopaedic Oncology, Mayo Clinic, Rochester, MN, USA.

Peter W M Chung (PWM)

Radiation Oncology, Princess Margaret Hospital, University of Toronto, Toronto, ON, Canada.

Anthony M Griffin (AM)

University Musculoskeletal Oncology Unit, Sinai Health System, Division of Orthopaedic Surgery, Department of Surgery, University of Toronto, Toronto, ON, Canada.

Peter Ferguson (P)

University Musculoskeletal Oncology Unit, Sinai Health System, Division of Orthopaedic Surgery, Department of Surgery, University of Toronto, Toronto, ON, Canada.

Jay S Wunder (JS)

University Musculoskeletal Oncology Unit, Sinai Health System, Division of Orthopaedic Surgery, Department of Surgery, University of Toronto, Toronto, ON, Canada.

Kim M Tsoi (KM)

University Musculoskeletal Oncology Unit, Sinai Health System, Division of Orthopaedic Surgery, Department of Surgery, University of Toronto, Toronto, ON, Canada.

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Classifications MeSH