Extrameningeal solitary fibrous tumors-surgery alone or surgery plus perioperative radiotherapy: A retrospective study from the global solitary fibrous tumor initiative in collaboration with the Sarcoma Patients EuroNet.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 29 11 2019
revised: 26 03 2020
accepted: 30 03 2020
pubmed: 22 4 2020
medline: 14 5 2021
entrez: 22 4 2020
Statut: ppublish

Résumé

Solitary fibrous tumor (SFT) is a rare mesenchymal malignancy. Although surgery is potentially curative, the local relapse risk is high after marginal resections. Given the lack of prospective clinical trial data, the objective of the current study was to better define the role of perioperative radiotherapy (RT) in various SFT presentations by location. This was retrospective study performed across 7 sarcoma centers. Clinical information was retrieved from all adult patients with extrameningeal, primary, localized SFT who were treated between 1990 and 2018 with surgery alone (S) compared with those who also received perioperative RT (S+RT). Differences in treatment characteristics between subgroups were tested using analysis of variance statistics and propensity score matching. Local control and overall survival rates were calculated from the start of treatment until progression or death from any cause. Of all 549 patients, 428 (78%) underwent S, and 121 (22%) underwent S+RT. The median follow-up was 52 months. After correction for mitotic count and surgical margins, S+RT was significantly associated with a lower risk of local progression (hazard ratio, 0.19: P = .029), an observation further confirmed by propensity score matching (P = .012); however, this association did not translate into an overall survival benefit. The results from this retrospective study investigating perioperative RT in patients with primary extrameningeal SFT suggest that combining RT with surgery in the management of this patient population is significantly associated with a reduced risk of local failures, especially in patients who have less favorable resection margins and in those who have tumors with a high mitotic count.

Sections du résumé

BACKGROUND
Solitary fibrous tumor (SFT) is a rare mesenchymal malignancy. Although surgery is potentially curative, the local relapse risk is high after marginal resections. Given the lack of prospective clinical trial data, the objective of the current study was to better define the role of perioperative radiotherapy (RT) in various SFT presentations by location.
METHODS
This was retrospective study performed across 7 sarcoma centers. Clinical information was retrieved from all adult patients with extrameningeal, primary, localized SFT who were treated between 1990 and 2018 with surgery alone (S) compared with those who also received perioperative RT (S+RT). Differences in treatment characteristics between subgroups were tested using analysis of variance statistics and propensity score matching. Local control and overall survival rates were calculated from the start of treatment until progression or death from any cause.
RESULTS
Of all 549 patients, 428 (78%) underwent S, and 121 (22%) underwent S+RT. The median follow-up was 52 months. After correction for mitotic count and surgical margins, S+RT was significantly associated with a lower risk of local progression (hazard ratio, 0.19: P = .029), an observation further confirmed by propensity score matching (P = .012); however, this association did not translate into an overall survival benefit.
CONCLUSIONS
The results from this retrospective study investigating perioperative RT in patients with primary extrameningeal SFT suggest that combining RT with surgery in the management of this patient population is significantly associated with a reduced risk of local failures, especially in patients who have less favorable resection margins and in those who have tumors with a high mitotic count.

Identifiants

pubmed: 32315454
doi: 10.1002/cncr.32911
pmc: PMC7318349
doi:

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

3002-3012

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.

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Auteurs

Rick L Haas (RL)

Department of Radiotherapy, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Radiation Oncology, The Leiden University Medical Center, Leiden, The Netherlands.

Iris Walraven (I)

Department of Radiotherapy, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Estelle Lecointe-Artzner (E)

Sarcoma Patients EuroNet Association (SPAEN), Friedberg, Germany.

Winan J van Houdt (WJ)

Department of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Dirk Strauss (D)

Sarcoma Unit, Department of Surgery, The Royal Marsden Hospital, London, United Kingdom.

Yvonne Schrage (Y)

Department of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Sarcoma Unit, Department of Surgery, The Royal Marsden Hospital, London, United Kingdom.
Department of Surgical Oncology, The Leiden University Medical Center, Leiden, The Netherlands.

Andrew J Hayes (AJ)

Sarcoma Unit, Department of Surgery, The Royal Marsden Hospital, London, United Kingdom.

Chandrajit P Raut (CP)

Division of Surgical Oncology, Department of Surgery, Brigham and Women's Hospital, Boston, Massachusetts.
Center for Sarcoma and Bone Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.

Mark Fairweather (M)

Division of Surgical Oncology, Department of Surgery, Brigham and Women's Hospital, Boston, Massachusetts.
Center for Sarcoma and Bone Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.

Elizabeth H Baldini (EH)

Center for Sarcoma and Bone Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.
Department of Radiation Oncology, Brigham and Women's Hospital, Boston, Massachusetts.

Alessandro Gronchi (A)

Department of Surgical Oncology, IRCCS Foundation, National Cancer Institute, Milan, Italy.

Laura De Rosa (L)

Department of Surgical Oncology, IRCCS Foundation, National Cancer Institute, Milan, Italy.

Anthony M Griffin (AM)

Department of Orthopedic Surgery, Sarcoma Unit, Mount Sinai Hospital, Toronto, Ontario, Canada.

Peter C Ferguson (PC)

Department of Orthopedic Surgery, Sarcoma Unit, Mount Sinai Hospital, Toronto, Ontario, Canada.

Jay Wunder (J)

Department of Orthopedic Surgery, Sarcoma Unit, Mount Sinai Hospital, Toronto, Ontario, Canada.

Michiel A J van de Sande (MAJ)

Department of Orthopedic Oncology, The Leiden University Medical Center, Leiden, The Netherlands.

Augustinus D G Krol (ADG)

Department of Radiation Oncology, The Leiden University Medical Center, Leiden, The Netherlands.

Jacus Skoczylas (J)

Department of Surgical Oncology, The Maria Sklodowska-Curie Institute Oncology Center, Warsaw, Poland.

Claudia Sangalli (C)

Radiation Oncology, IRCCS Foundation, National Cancer Institute, Milan, Italy.

Silvia Stacchiotti (S)

Adult Mesenchymal and Rare Tumor Unit, Medical Oncology, IRCCS Foundation, National Cancer Institute, Milan, Italy.

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Classifications MeSH