NCT05522660Recruiting
Immunotherapy or Targeted Therapy With or Without Stereotactic Radiosurgery for Patients With Brain Metastases From Melanoma or Non-small Cell Lung Cancer
Summary
The primary objective of the study is to assess the efficacy in terms of CNS-specific PFS of the combination of standard systemic treatment plus SRS vs. standard systemic treatment alone in patients with newly diagnosed and untreated (except for surgery) asymptomatic or oligosymptomatic brain metastases from melanoma or NSCLC. This proposed randomised phase III clinical study addresses one of the most controversial issues in the current approach to patients with brain mets: the timing of SRS in patients eligible for systemic immune checkpoint inhibition or targeted therapy in order to guide therapeutic options as to what strategy allows the best compromise between best survival and best QoL.
Inclusion criteria
• Newly diagnosed, previously untreated (except for surgery, see below) asymptomatic or oligo-symptomatic brain metastases, e.g., controlled symptomatic seizure disorder. Note: patients with neurological symptoms or signs that require more than a stable dose of 4 mg dexamethasone equivalent for more than one week are not considered oligo-symptomatic. • Requirements for brain metastases: • Brain metastases must be previously untreated, except for surgery. • Prior surgery (including biopsies, resection, and cyst aspiration) for brain metastases is allowed. Residual and measurable disease after surgery is not required, but surgery must have confirmed the diagnosis. An MRI performed within 72 hours post-surgery should be available. • Number and size of metastases at diagnosis of brain metastases: • Maximum 1-10 brain metastases at screening • At least one brain metastasis must be of ≥5 mm in diameter • In case of 1-4 brain metastases: • Longest diameter of largest brain metastasis must be ≤30 mm • In case of 5-10 brain metastases: • Largest metastasis must be ≤10 mL in volume and longest diameter must be ≤30 mm • Maximum cumulative brain metastases volume must be ≤30 mL • Primary disease of histologically confirmed (from primary tumour or from a metastatic lesion, including in the brain) melanoma or NSCLC • Requirements for patients with melanoma: • Prior treatment, including treatment with immune-checkpoint inhibitors is permitted, but brain metastases must be newly diagnosed and previously untreated (except for surgery). • BRAF-mutation status, locally assessed, should be known (previous adjuvant BRAF-targeted therapy is allowed). • Requirements for patients with NSCLC: • Newly diagnosed, treatment-naïve (except for prior surgery) metastatic NSCLC, with or without a targetable oncogenic driver alteration. • Known PD-L1 expression status (from primary tumour or from a metastatic lesion, including brain) • Known driver mutation status (from primary tumour or from a metastatic lesion, including brain). • Age of 18 years or older • Karnofsky performance status of 60 or more • Life expectancy \>12 weeks • Patients must be candidates for systemic treatment, within the defined cohorts (melanoma: cohorts 1a and 1b; NSCLC: cohorts 2a and 2b). • Women of childbearing potential, including women who had their last menstruation in the last 2 years, must have a negative urinary or serum pregnancy test within 7 days before randomisation. • Written IC for study participation must be signed and dated by the patient and the investigator prior to any study-related intervention.
Exclusion criteria
• Confirmed or probable leptomeningeal metastases according to EANO ESMO criteria • Symptomatic brain metastases at time of randomisation, e.g., neurological symptoms or signs that require more than a stable dose of 4 mg dexamethasone equivalent for more than one week. • Patients must be off steroids or on a stable dose of ≤4 mg dexamethasone equivalent at randomisation. • Patients experiencing seizures controlled by anti-epileptic drugs are eligible. • Prior whole brain irradiation or focal radiation therapy to the brain • Prior systemic treatment for brain metastases • Contra-indication for SRS • Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements. • Women who are pregnant or in the period of lactation. • Sexually active men and women of childbearing potential who are not willing to use an effective contraceptive method during the study.
Contacts
The trial team's contact details are shown on request.
See the official trial record- Status
- Recruiting
- Phase
- Phase 3
- Study type
- Interventional
- Countries
- Switzerland, Italy, Netherlands, Spain, United Kingdom
- Sponsor
- ETOP IBCSG Partners Foundation(Network / cooperative)
- Protocol no.
- ETOP 19-21
- Conditions
- Non-Small Cell Lung Cancer, Melanoma
- Interventions
- Radiation, Drug
Treatments studied
- Stereotactic radiosurgery
- Immune checkpoint inhibitor
Collaborators
USZ Foundation
Locations · 14
- Bern, SwitzerlandInselspitalRecruiting at this site
- Winterthur, SwitzerlandKantonsspital WinterthurRecruiting at this site
- Zurich, SwitzerlandUniversitätsspital ZürichRecruiting at this site
- Naples, ItalyIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale"Recruiting at this site
- Perugia, ItalySanta Maria della Misericordia HospitalRecruiting at this site
- Roma, ItalyIstituto Nazionale Tumori "Regina Elena"Recruiting at this site
- Rome, ItalyPoliclinico Umberto 1Recruiting at this site
- Siena, ItalyAzienda ospedaliero-universitaria Senese SienaRecruiting at this site
- Amsterdam, NetherlandsNKI-AVLRecruiting at this site
- Barcelona, SpainVall Hebron Institute of Oncology (VHIO)Recruiting at this site
- Majadahonda, SpainHospital Puerta de HierroRecruiting at this site
- Valencia, SpainHospital La FeRecruiting at this site
- London, United KingdomRoyal Marsden (Sutton)Recruiting at this site
- Manchester, United KingdomChristie NHS ManchesterRecruiting at this site
In total, worldwide, 14 of the 15 sites listed in the registry are recruiting; the other one is not currently recruiting.
Site status per the ClinicalTrials.gov registry (last update posted: April 27, 2026).
This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.
See also
Other versions
These results are indicative and do not replace medical advice — discuss them with your doctor.