A Large, Multicenter, Retrospective Study on Efficacy and Safety of Stereotactic Body Radiotherapy (SBRT) in Oligometastatic Ovarian Cancer (MITO RT1 Study): A Collaboration of MITO, AIRO GYN, and MaNGO Groups.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
02 2020
Historique:
received: 20 04 2019
accepted: 23 08 2019
entrez: 12 2 2020
pubmed: 12 2 2020
medline: 22 6 2021
Statut: ppublish

Résumé

Recent studies have reported improvement of outcomes (progression-free survival, overall survival, and prolongation of androgen deprivation treatment-free survival) with stereotactic body radiotherapy (SBRT) in non-small cell lung cancer and prostate cancer. The aim of this retrospective, multicenter study (MITO RT-01) was to define activity and safety of SBRT in a very large, real-world data set of patients with metastatic, persistent, and recurrent ovarian cancer (MPR-OC). The endpoints of the study were the rate of complete response (CR) to SBRT and the 24-month actuarial local control (LC) rate on "per-lesion" basis. The secondary endpoints were acute and late toxicities and the 24-month actuarial late toxicity-free survival. Objective response rate (ORR) included CR and partial response (PR). Clinical benefit (CB) included ORR and stable disease (SD). Toxicity was evaluated by the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC) and Common Terminology Criteria for Adverse Events (CTCAE) scales, according to center policy. Logistic and Cox regression were used for the uni- and multivariate analysis of factors predicting clinical CR and actuarial outcomes. CR, PR, and SD were observed in 291 (65.2%), 106 (23.8%), and 33 (7.4%) lesions, giving a rate of CB of 96.4%. Patient aged ≤60 years, planning target volume (PTV) ≤18 cm This study confirms the activity and safety of SBRT in patients with MPR-OC and identifies clinical and treatment parameters able to predict CR and LC rate. This study aimed to define activity and safety of stereotactic body radiotherapy (SBRT) in a very large, real life data set of patients with metastatic, persistent, recurrent ovarian cancer (MPR-OC). Patient age <60 years, PTV <18 cm

Sections du résumé

BACKGROUND
Recent studies have reported improvement of outcomes (progression-free survival, overall survival, and prolongation of androgen deprivation treatment-free survival) with stereotactic body radiotherapy (SBRT) in non-small cell lung cancer and prostate cancer. The aim of this retrospective, multicenter study (MITO RT-01) was to define activity and safety of SBRT in a very large, real-world data set of patients with metastatic, persistent, and recurrent ovarian cancer (MPR-OC).
MATERIALS AND METHODS
The endpoints of the study were the rate of complete response (CR) to SBRT and the 24-month actuarial local control (LC) rate on "per-lesion" basis. The secondary endpoints were acute and late toxicities and the 24-month actuarial late toxicity-free survival. Objective response rate (ORR) included CR and partial response (PR). Clinical benefit (CB) included ORR and stable disease (SD). Toxicity was evaluated by the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC) and Common Terminology Criteria for Adverse Events (CTCAE) scales, according to center policy. Logistic and Cox regression were used for the uni- and multivariate analysis of factors predicting clinical CR and actuarial outcomes.
RESULTS
CR, PR, and SD were observed in 291 (65.2%), 106 (23.8%), and 33 (7.4%) lesions, giving a rate of CB of 96.4%. Patient aged ≤60 years, planning target volume (PTV) ≤18 cm
CONCLUSIONS
This study confirms the activity and safety of SBRT in patients with MPR-OC and identifies clinical and treatment parameters able to predict CR and LC rate.
IMPLICATIONS FOR PRACTICE
This study aimed to define activity and safety of stereotactic body radiotherapy (SBRT) in a very large, real life data set of patients with metastatic, persistent, recurrent ovarian cancer (MPR-OC). Patient age <60 years, PTV <18 cm

Identifiants

pubmed: 32043791
doi: 10.1634/theoncologist.2019-0309
pmc: PMC7011643
doi:

Substances chimiques

Androgen Antagonists 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e311-e320

Informations de copyright

© AlphaMed Press 2019.

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Auteurs

Gabriella Macchia (G)

Fondazione "Giovanni Paolo II," Unità Operativa di Radioterapia, Università Cattolica del Sacro Cuore, Campobasso, Italy.

Roberta Lazzari (R)

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

Nicoletta Colombo (N)

Division of Medical Gynecologic Oncology, IEO European Institute of Oncology, IRCCS and University of Milan-Bicocca, Milan, Italy.

Concetta Laliscia (C)

Department of Translational Medicine, Division of Radiation Oncology, University of Pisa, Pisa, Italy.

Giovanni Capelli (G)

Department of Human Sciences, Society and Health, University of Cassino and Southern Lazio, Cassino, Italy.

Giuseppe Roberto D'Agostino (GR)

Department of Radiotherapy and Radiosurgery, Humanitas Clinical and Research Hospital, IRCSS, Rozzano, Milan, Italy.

Francesco Deodato (F)

Fondazione "Giovanni Paolo II," Unità Operativa di Radioterapia, Università Cattolica del Sacro Cuore, Campobasso, Italy.

Ernesto Maranzano (E)

Radiation Oncology Centre, S. Maria Hospital, Terni, Italy.

Edy Ippolito (E)

Department of Radiation Oncology, Campus Bio-Medico University, Rome, Italy.

Sara Ronchi (S)

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

Fabiola Paiar (F)

Department of Translational Medicine, Division of Radiation Oncology, University of Pisa, Pisa, Italy.

Marta Scorsetti (M)

Department of Radiotherapy and Radiosurgery, Humanitas Clinical and Research Hospital, IRCSS, Rozzano, Milan, Italy.
Humanitas University, Department of Biomedical Sciences, Rozzano, Milano, Italy.

Savino Cilla (S)

Fondazione "Giovanni Paolo II," Unità Operativa di Fisica Medica, Università Cattolica del Sacro Cuore, Campobasso, Italy.

Rossana Ingargiola (R)

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

Alessandra Huscher (A)

U.O. di Radioterapia Oncologica "Guido Berlucchi," Fondazione Poliambulanza, Brescia, Italy.

Anna Maria Cerrotta (AM)

Radiotherapy Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Andrei Fodor (A)

Department of Radiation Oncology, San Raffaele Scientific Institute, Milan, Italy.

Lisa Vicenzi (L)

Department of Oncology and Radiotherapy, Azienda Ospedaliera Universitaria Ospedali Riuniti, Ancona, Italy.

Donatella Russo (D)

Radiotherapy Unit, Ospedale "Vito Fazzi", Lecce, Italy.

Simona Borghesi (S)

Radiotherapy Department, Azienda USL Toscana sud est, San Donato Hospital-Arezzo, Italy.

Elisabetta Perrucci (E)

Radiation Oncology Section, University of Perugia and Perugia General Hospital, Perugia, Italy.

Sandro Pignata (S)

Istituto Nazionale Tumori di Napoli, Fondazione Pascale IRCCS, Naples, Italy.

Cynthia Aristei (C)

Radiation Oncology Section, University of Perugia and Perugia General Hospital, Perugia, Italy.

Alessio Giuseppe Morganti (AG)

Department of Experimental, Diagnostic and Specialty Medicine - DIMES, University of Bologna, S. Orsola-Malpighi Hospital, Bologna, Italy.

Giovanni Scambia (G)

Fondazione Policlinico Universitario A. Gemelli, IRCCS, Unità Operativa Complessa Ginecologia Oncologica, Dipartimento per la Salute della Donna e del Bambino e della Salute Pubblica, Roma, Italy.
Università Cattolica del Sacro Cuore, Istituto di Ginecologia e Ostetricia, Roma, Italy.

Vincenzo Valentini (V)

Fondazione "Giovanni Paolo II," Unità Operativa di Radioterapia, Università Cattolica del Sacro Cuore, Campobasso, Italy.
Fondazione Policlinico Universitario A. Gemelli, IRCCS, Unità Operativa Complessa di Radioterapia, Dipartimento di Scienze Radiologiche, Radioterapiche ed Ematologiche, Roma, Italy.
Università Cattolica del Sacro Cuore, Istituto di Radiologia, Roma, Italy.

Barbara Alicja 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.

Gabriella Ferrandina (G)

Fondazione Policlinico Universitario A. Gemelli, IRCCS, Unità Operativa Complessa Ginecologia Oncologica, Dipartimento per la Salute della Donna e del Bambino e della Salute Pubblica, Roma, Italy.
Università Cattolica del Sacro Cuore, Istituto di Ginecologia e Ostetricia, Roma, Italy.

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