This is a prospective, multicenter, Phase II study aimed at defining the activity and safety of SBRT in MPR-OC. Clinical and imaging data as well as SBRT parameters would be analyzed with the aim to identify potential predictors of response to treatment and clinical outcome.
Stereotactic Body Radiotherapy (SBRT) represents the cutting edge within high conformal and modulated radiotherapy techniques; it can provide high local control (LC) for curative-intent of low burden metastatic, persistent and metastatic lesions in face of minimal acute and late toxicities. SBRT is amenable even in patients who had already been managed by radiotherapy. In addition, SBRT has been shown to be active in chemoresistant disease, and potentially able to mount immune response through the release of tumor neoantigens after cell killing, thus allowing to synergize with immunotherapeutic approaches. SBRT has been widely adopted in the clinical setting of oligometastatic/persistent/recurrent (MPR) disease (up to \<5 lesions) in several malignancies including also ovarian cancer (OC); the recently published retrospective, multicenter Italian study (MITO-RT1) has confirmed the activity and safety of SBRT in MPR OC, thus providing a model able to predict the higher chance of complete response of tumor lesions to SBRT, and local control rate. The MITO-RT3/RAD trial is a prospective, Italian multicenter Phase II study aimed at evaluating the activity and safety of SBRT in MPR-OC patients. Clinical and imaging data, as well as SBRT technical parameters, would be analyzed with the aim to identify potential predictors of response to treatment and clinical outcome: in this context, additional insights into the tissue features of tumor lesions would be of clinical interest in the context of the personalized treatment, as testified by studies demonstrating that image-based quantitative features from pre-treatment imaging could predict clinical outcomes in several malignancies. Furthermore, given the crucial role played by the mutational status of BRCA 1/2 genes in this disease, the assessment of BRCA gene status was considered mandatory, thus representing inclusion criteria. The study will include patients with oligo-metastatic/persistent/recurrent lesions (MPR) from OC patients for which salvage surgery or other local therapies resulted not feasible, as per relative contraindication to further systemic therapy because of serious comorbidities, as per previous severe toxicity, unavailability of potentially active chemotherapy, or patient refusal of systemic therapy
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
376
All patients accrued will be treated with SBRT to all sites of active metastatic disease as per CT scan or PET/CT and/or MRI. A range of schedules and doses are provided, it is advised that the maximum dose that can be achieved whilst meeting the organs at risk planning constraints is prescribed.
Responsible Research Hospital
Campobasso, CB, Italy
S.C. di Radioterapia Oncologica-Azienda Sanitaria locale
Biella, Italy
Azienda Ospedaliera "Cannizzaro"
Catania, Italy
Clinical complete response to SBRT by imaging
Radiologic response will be evaluated by morphological (contrast-enhanced CT scan and/or MRI) or functional imaging modalities (18F-fluorodeoxyglucose-PET) and classified according to the RECIST (version 1.1) or PERCIST criteria.
Time frame: Assessment of Clinical complete response at six months
2-yr actuarial LC rate
progression of disease inside SBRT field on a per lesion basis
Time frame: 2 years
2-yr progression-free survival
progression of disease out of SBRT field
Time frame: 2 years
2-yr overall survival
patient survival
Time frame: 2 years
treatment free interval
time without any new treatment start after SBRT
Time frame: 2 years
rate of toxicity
SBRT acute and late toxicity rate
Time frame: 2 years
2-yr actuarial late toxicity free survival
actuarial evaluation of late toxicity
Time frame: 2 years
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Azienda sanitaria locale Lanciano Vasto Chieti
Chieti, Italy
Ospedale Vito Fazzi
Lecce, Italy
Department of Radiation Oncology, IRCCS San Raffaele Scientific Institute
Milan, Italy
Humanitas Clinical and Research Center-IRCCS
Milan, Italy
Azienda USL - IRCCS di Reggio Emilia
Reggio Emilia, Italy
Campus Biomedico
Roma, Italy
Policlinico A. Gemelli, IRCCS
Roma, Italy
...and 4 more locations