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The study's primary objective is the evaluation of toxicities reported during RS or HFSRT in patients with brain metastases from NSCLC undergoing immunotherapy (Safety), with particular reference to the rate of symptomatic radionecrosis and intralesional hemorrhage. Others primary objectives of the study are the Feasibility and the intracranial control of the disease, both local (site radiotherapy treatment) and at a distance (intracranial, but at a distance from the site of the disease treated with stereotaxic radiotherapy). The secondary objectives concern quality assessment of life of the patients under study (Quality Of Life, QoL).
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Inclusion criteria
Age> 18 years
Histological or cytological diagnosis (possibility of PDL-1 determination) of NSCLC
Brain disease assessable according to iRANO criteria
Radiation therapy on brain metastases within 4 weeks before or after infusion of immunotherapy in the following settings
brain metastases at initio brain metastases treated with RS + 1st line therapy
Brain metastases as I progression after I line of systemic therapy CHT, IT or CHTIT regardless of whether or not the same line is continued (treatment Beyond progression) or shift to the next line;
Brain metastases as II progression after II line of systemic therapy (CHT, IT) regardless of whether it is continued or not of the same line (treatment beyond progression) or shift to the next line.
Diagnostic brain MRI for brain metastases within one month of treatment stereotactic
Esclusion criteria:
Exclusion criteria
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Data sourced from clinicaltrials.gov
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