European Institute of Oncology, Milan
Milan, Mi, 20141, Italy
Location contact
Lorenzo Colombi, MD
CONTACT
Samantha Dicuonzo, MD
CONTACT
NCT Number: NCT07691255
Melanoma is a type of cancer that can spread to the brain, making the disease harder to treat and worsening both survival and quality of life.
In recent years, treatments have improved significantly thanks to advances in surgery, radiotherapy, immunotherapy, and targeted therapy. These new treatments have greatly increased survival rates for patients with metastatic melanoma.
This study focuses on stereotactic radiosurgery, a highly precise form of radiotherapy used to treat brain metastases. Researchers want to better understand how this treatment works when combined with immunotherapy or targeted therapy, and whether the timing and sequence of treatments can improve outcomes.
Between 2026 and 2028, patients treated at the IEO for melanoma brain metastases will be observed and their clinical data collected. The goal is to improve future treatment strategies and help doctors choose the best therapeutic approach for each patient.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Milan, Mi, 20141, Italy
Lorenzo Colombi, MD
CONTACT
Samantha Dicuonzo, MD
CONTACT
The therapeutic landscape of metastatic melanoma has undergone a radical transformation in the last decade, largely due to the recent introduction of immune checkpoint inhibitors (IT) and targeted therapies (TTs), and advances in surgery and radiotherapy (RT), which have changed the outlook of patients with melanoma brain metastasis.
Radiation therapy has been and remains an important component of treatment for patients with melanoma brain metastases.
Particularly, stereotactic radiosurgery (SRS), highly precise RT technique, for single or a small number of metastases, has emerged as a crucial component in the management of melanoma brain metastases, with whole brain RT usually reserved for selected patients who have widespread intracranial metastatic disease. SRS relies on the delivery of concentrated, high doses of radiation to one or more metastatic brain lesions of otherwise radio-resistant tumors such as melanoma, providing effective local control (LC) of the disease while minimizing damage to surrounding healthy tissue. SRS can be employed both as an independent primary local therapy, allowing a swifter transition to systemic therapy compared to classic surgical resection and as a salvage procedure after ineffective systemic treatment when the number of MBMs remains below 5-10 and their size is below 3 cm.
A recent systematic review of RT alone for MBMs reported a median survival of 7.5 months (IQR-6.7-9.0-months) after SRS and 3.5 months (IQR-2.4-4.0-months) after whole brain RT.
Although these advances have successfully improved the outcomes of patients with metastatic melanoma, its management remains challenging and complex, requiring a multidisciplinary approach that integrates surgery, systemic therapy, and RT to optimize patient outcomes.
Ongoing investigations in this field are now focused on determining the best strategies to combine RT modalities with systemic therapies (IT and TT), emphasizing the potential for synergistic effects that enhance treatment efficacy. However, data on optimal sequencing and toxicity management, particularly in the context of radiosurgery, remain limited and require careful evaluation. The approach of combining RT with IT or TT has therefore become established in practice but this strategy has not been evaluated in randomized controlled trials. Clinical guidelines vary in the strength of their recommendations for combining different treatments. Studies differ in terms of patient selection, the extent of extracranial disease, the number of lesions treated, and the definitions of concurrent versus non-concurrent therapies. These differences make it challenging to draw definitive conclusions about the optimal treatment strategy for melanoma brain metastases.
In this prospective observational study, the investigators aim to analyse the impact of RT in a well selected population of patient receiving SRS at the European Institute of Oncology- IRCCS- Milan- as first local approach for MBMs, in combination with different type and timing of systemic treatment.
By analysing data from patients treated with CyberKnife from 2026 to 2028, the investigatorsseek to provide insights into the effectiveness of SRS according LC, overall survival (OS) and progression-free survival (PFS) in this patient population.
The investigators aim to investigate also potential prognostic factors including demographic, clinical, and therapeutic factors, with a focus on the influence of concurrent versus non-concurrent systemic therapies.
Through this prospective observational study, the investigators aim both to contribute to the growing body of evidence supporting the use of SRS as a viable treatment option for patients with MBMs and to identify factors that may enhance treatment efficacy and improve patient outcomes.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From the end of radiotherapy through study completion, every three months.
The primary objective of the study is to estimate the 1-year intracranial in-field progression-free survival (IIFPFS). Based on results from a retrospective analysis conducted on patients treated at our institution, we expect a 1-year IIFPFS of approximately 57%. With a sample size of 50 patients, the 95% confidence interval (CI) for the 1-year IIFPFS is expected to have an approximate width of 27% (i.e. 43.5-70.5%).
Time frame: From the end of radiotherapy through study completion, every three months.
Defined as the time from the end of radiotherapy to death
Time frame: From the end of radiotherapy through study completion, every three months.
Defined as the time from the end of radiotherapy to disease progression (either global intracranial or extracranial) or death, whichever occurred first.
Time frame: From the end of radiotherapy through study completion, every three months.
defined as the time from the end of radiotherapy to intracranial out-field progression
Time frame: From the end of radiotherapy through study completion, every three months.
defined as the time from the end of radiotherapy to the global intracranial progression
Time frame: From the end of radiotherapy through study completion, every three months.
defined as the time from the end of radiotherapy to the extracranial progression
Time frame: From the end of radiotherapy through study completion, every three months.
Defined as the absence of local progression (complete response, partial response, or stable disease) at the last radiological assessment. The LC rate was calculated among evaluable lesions and reported as a proportion with its 95% confidence interval (CI).
Time frame: From the end of radiotherapy through study completion, every three months.
Stereotactic radiotherapy related adverse events according CTCAE V5.0 and data about radionecrosis will be systematically collected allong the follow up (every trhee months)
Time frame: From the baseline (start of radiotehrapy), to the end of study (12 months), every three months.
For EORTC QLQ BN20, 20 items will be completed (score 1-4)
Time frame: From the baseline (start of radiotehrapy), to the end of study (12 months), every three months.
For EORTC QLQ C30, 30 items will be completed (score 1-4).
Contact information is provided by the study sponsor or research team.
Lorenzo Colombi, MD
CONTACT
Samantha Dicuonzo, MD
CONTACT
European Institute of Oncology
Other
Impact of Stereotactic Radiosurgery With Cyberknife In Patients With Brain Melanoma Metastases In The Era Of New Drugs
Acronym: MELCY
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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