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Clinical Trial · NCT05111197
Overview
At present, it is recommended to continue immunotherapy until progression or unacceptable toxicity. However, only a minority of patients benefits from a durable response and most see the disease progress despite several months of control under immunotherapy. Multimodal approaches have been developed to improve their prognosis. This study, randomized, open-label study aims to evaluate the impact of addition of ablative radiotherapy on OS of patients with NSCLC and oligometastatic lesions and treated by immunotherapy in first line (potentially associated with chemotherapy) or beyond. Stereotactic radiotherapy will be performed on a maximum of 5 residual hypermetabolic lesions seen on 18F-FDG PET / CT, in patients responding to immunotherapy (or with a stable disease) for at least 6 months.
Sponsor
Institut Cancerologie de l'Ouest
Phase
Phase 3
Contacts
Sandrine HIRET, MD
sandrine.hiret@ico.unicancer.fr
+33 (0)2 40 67 99 78
Emilie DEBEAUPUIS
emilie.debeaupuis@ico.unicancer.fr
ClinicalTrials.gov
NCT05111197Drug / Compound
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