Oligometastatic Sarcoma treated with Curative intent Ablative Radiotherapy (OSCAR): a multicenter study on behalf of AIRO (Italian Association of Radiotherapy and clinical Oncology).

oligometastasis soft tissue sarcoma stereotactic ablative radiation therapy

Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
30 Dec 2023
Historique:
received: 01 09 2023
revised: 18 12 2023
accepted: 29 12 2023
medline: 2 1 2024
pubmed: 2 1 2024
entrez: 1 1 2024
Statut: aheadofprint

Résumé

Stereotactic Ablative Radiotherapy (SABR) is emerging as a valid alternative to surgery in the oligometastatic setting in soft tissue sarcomas (STS), although robust data are lacking. The aim of this study is to evaluate toxicity and efficacy of SABR in oligometastatic STS. This is a retrospective multicenter study including adult patients affected by stage IV STS, treated with SABR for a maximum of 5 cranial or extracranial metastases in up to 3 different organs. SABR was delivered with ablative purposes. Study endpoints were overall survival (OS), local control (LC), distant progression free survival (DPFS), time to polymetastatic progression (TTPP), time to new systemic therapy (TTNS) and toxicity. From 10 Italian RT centers, 138 patients (202 metastases) treated between 2010 and 2022 were enrolled in the study. Treatment was generally well tolerated, no acute or late toxicity ≥ G3 was recorded. Median follow up was 42.5 months. Median OS was 39.7 months. Actuarial OS at 1 and 2 years was 91.5% and 72.7%. Actuarial LC at 1 and 2 years was 94.8% and 88.0%. Median DPFS was 9.7 months. Actuarial DPFS at 1 and 2 years was 40.8% and 19.4%. CONCLUSION SABR is a safe and effective approach for the treatment of oligometastatic sarcoma. One out of 5 patients is free of progression at 2-years.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Stereotactic Ablative Radiotherapy (SABR) is emerging as a valid alternative to surgery in the oligometastatic setting in soft tissue sarcomas (STS), although robust data are lacking. The aim of this study is to evaluate toxicity and efficacy of SABR in oligometastatic STS.
MATERIALS AND METHODS METHODS
This is a retrospective multicenter study including adult patients affected by stage IV STS, treated with SABR for a maximum of 5 cranial or extracranial metastases in up to 3 different organs. SABR was delivered with ablative purposes. Study endpoints were overall survival (OS), local control (LC), distant progression free survival (DPFS), time to polymetastatic progression (TTPP), time to new systemic therapy (TTNS) and toxicity.
RESULTS RESULTS
From 10 Italian RT centers, 138 patients (202 metastases) treated between 2010 and 2022 were enrolled in the study. Treatment was generally well tolerated, no acute or late toxicity ≥ G3 was recorded. Median follow up was 42.5 months. Median OS was 39.7 months. Actuarial OS at 1 and 2 years was 91.5% and 72.7%. Actuarial LC at 1 and 2 years was 94.8% and 88.0%. Median DPFS was 9.7 months. Actuarial DPFS at 1 and 2 years was 40.8% and 19.4%. CONCLUSION SABR is a safe and effective approach for the treatment of oligometastatic sarcoma. One out of 5 patients is free of progression at 2-years.

Identifiants

pubmed: 38163485
pii: S0167-8140(23)09385-4
doi: 10.1016/j.radonc.2023.110078
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110078

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

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

D Franceschini (D)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy. Electronic address: davide.franceschini@humanitas.it.

D Greto (D)

Radiation Oncology Unit, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.

S Dicuonzo (S)

Division of Radiotherapy, IEO, European Institute of Oncology IRCCS, Milan, Italy.

F Navarria (F)

Radiation Oncology Department, IRCCS Centro di Riferimento Oncologico, Aviano, Italy.

M Federico (M)

Radiotherapy Unit, Casa di Cura Macchiarella, Palermo, Italy.

M La Vecchia (M)

Radiotherapy Unit, Casa di Cura Macchiarella, Palermo, Italy.

C Sangalli (C)

Department of Radiation Therapy, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

A Allajbej (A)

Department of Radiation Therapy, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

L Di Cristina (L)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, 20090 Milan, Italy.

R Mazzola (R)

Advanced Radiation Oncology Department, IRCCS Sacro Cuore Don Calabria Hospital, Cancer Care Center, 37034, Negrar Di Valpolicella, Verona, Italy.

A Pontoniero (A)

Radiation Oncology Unit, A.O.U. "G. Martino", Messina, Italy; Department of Biomedical, Dental Science and Morphological and Functional Images, University of Messina, Messina, Italy.

G Montesi (G)

Radiation Therapy Unit ULSS5 Veneto, Rovigo, Italy.

P Navarria (P)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy.

D Baldaccini (D)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy.

E Clerici (E)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy.

L Lo Faro (L)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, 20090 Milan, Italy.

C Franzese (C)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, 20090 Milan, Italy.

S Di Biase (S)

Radiation Therapy Unit ULSS5 Veneto, Rovigo, Italy.

S Pergolizzi (S)

Radiation Oncology Unit, A.O.U. "G. Martino", Messina, Italy; Department of Biomedical, Dental Science and Morphological and Functional Images, University of Messina, Messina, Italy.

F Alongi (F)

Advanced Radiation Oncology Department, IRCCS Sacro Cuore Don Calabria Hospital, Cancer Care Center, 37034, Negrar Di Valpolicella, Verona, Italy; University of Brescia, Brescia, Italy.

M Bignardi (M)

Department of Radiation Oncology, Fondazione Poliambulanza, 25124 Brescia, Italy.

I Fazio (I)

Radiotherapy Unit, Casa di Cura Macchiarella, Palermo, Italy.

M Mascarin (M)

Radiation Oncology Department, IRCCS Centro di Riferimento Oncologico, Aviano, Italy; AYA Oncology and Pediatric Radiotherapy Unit, IRCCS Centro di Riferimento Oncologico, Aviano, Italy.

B A Jereczek-Fossa (BA)

Division of Radiotherapy, IEO, European Institute of Oncology IRCCS, Milan, Italy; Department of Oncology and Hemato-oncology, University of Milan, Milan, Italy.

L Livi (L)

Radiation Oncology Unit, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy; Department of Biomedical, Experimental and Clinical Sciences, Serio" University of Florence, Florence, Italy.

M Scorsetti (M)

Department of Radiotherapy and Radiosurgery, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, 20090 Milan, Italy.

Classifications MeSH