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Melanoma (Skin Cancer)MELCYNCT07691255

MELanoma Brain Metastasis Treated With CYberknife

An observational study of Melanoma (Skin Cancer), run by European Institute of Oncology at 2 sites in Italy.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Melanoma (Skin Cancer)
How many people
50 participants
Where
2 sitesItaly
Study dates
25 Aug 2026to 1 Jan 2030
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients receiving stereotactic radiotherapy for melanoma brain metastases as first local approach. Target therapy and immunotherapy in combination or not will be permitted. Given the descriptive nature of the study, no formal sample size calculation was performed. The planned sample size was predefined according to historical data from the RT Division and reflects the expected number of eligible patients treated at our institution over the planned three-year study period. Based on these data, we anticipate enrolling approximately 50 patients.

Who may be able to join

  • Age > 18
  • Written informed consent for treatment and research purposes
  • Melanoma Brain Metastases (MBM) diagnosed with brain MRI/CT
  • MBM treatable with stereotactic radiotherapy
  • Systemic therapy (immunotherapy, target therapy, or both) is allowed, as concurrent or non-concurrent treatment with stereotactic radiotherapy

Who cannot join

  • Leptomeningeal neoplastic infiltration
  • Previous whole-brain radiotherapy or surgical removal of brain metastases
  • Patients with histological diagnosis of non-cutaneous melanoma (e.g. uveal melanoma)

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Samantha Dicuonzo, MD contact

+39 0257489037

samantha.dicuonzo@ieo.it

Lorenzo Colombi, MD contact

+39 0257489037

lorenzo.colombi@ieo.it

Italy2 sites, 2 recruiting
  • European Institute of Oncology, Milan

    Milan, Italy, 20141

    Recruiting
  • European Institute of Oncology, Milan

    Milan, Mi, 20141

    Samantha Dicuonzo, MD, +39 0257489037, samantha.dicuonzo@ieo.it

    Lorenzo Colombi, MD, +39 0257489037, lorenzo.colombi@ieo.it

    Recruiting

Other trials in Italy

About this study

Official title: Impact of Stereotactic Radiosurgery With Cyberknife In Patients With Brain Melanoma Metastases In The Era Of New Drugs

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.

Read more

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.

Read the detailed description

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.

Keywords
Stereotactic radiotherapy, Brain metastases
Medical subject headings
Melanoma, Brain Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07691255
Study groupRoleWhat they receive
Fifty patients receiving radiotherapy as first local approach for melanoma brain metastasesPatients will receive stereotactic radiotherapy as first local approach for melanoma brain metastases in combination with target therapy and/or immunotherapy. Patients will be followed every three months after the end of radiotherapy in order to collect oncological outcome, side effects and Quality of life data.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Intracranial in-field progression-free survival (IIFPFS)

    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%).

    Measured: From the end of radiotherapy through study completion, every three months.

Secondary outcomes (9)
  1. Overall survival (OS)

    Defined as the time from the end of radiotherapy to death

    Measured: From the end of radiotherapy through study completion, every three months.

  2. Progression-free survival (PFS)

    Defined as the time from the end of radiotherapy to disease progression (either global intracranial or extracranial) or death, whichever occurred first.

    Measured: From the end of radiotherapy through study completion, every three months.

  3. Intracranial out-field progression free survival (IOFPFS)

    defined as the time from the end of radiotherapy to intracranial out-field progression

    Measured: From the end of radiotherapy through study completion, every three months.

  4. Overall intracranial progression free survival (OIPFS)

    defined as the time from the end of radiotherapy to the global intracranial progression

    Measured: From the end of radiotherapy through study completion, every three months.

  5. Extracranial progression free survival (EPFS)

    defined as the time from the end of radiotherapy to the extracranial progression

    Measured: From the end of radiotherapy through study completion, every three months.

  6. Local control (LC)

    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).

    Measured: From the end of radiotherapy through study completion, every three months.

  7. Adverse events

    Stereotactic radiotherapy related adverse events according CTCAE V5.0 and data about radionecrosis will be systematically collected allong the follow up (every trhee months)

    Measured: From the end of radiotherapy through study completion, every three months.

  8. Quality of Life data (QoL) - EORTC QLQ BN20

    For EORTC QLQ BN20, 20 items will be completed (score 1-4)

    Measured: From the baseline (start of radiotehrapy), to the end of study (12 months), every three months.

  9. Quality of Life data (QoL) - EORTC QLQ C30 questionnaires.

    For EORTC QLQ C30, 30 items will be completed (score 1-4).

    Measured: From the baseline (start of radiotehrapy), to the end of study (12 months), every three months.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Jul 2026
  2. Study start25 Aug 2026
  3. Primary completion1 Jan 2030 (estimated)
  4. Study completion1 Jan 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07691255
Sponsor's protocol ID
UID 4996
Other IDs
L2-594
Acronym
MELCY
Status last verified
Aug 2026
First submitted
14 May 2026
Last updated
10 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Melanoma (Skin Cancer), run by European Institute of Oncology at 2 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 10 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Samantha Dicuonzo, MD (+39 0257489037, samantha.dicuonzo@ieo.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Intracranial in-field progression-free survival (IIFPFS) (time frame: From the end of radiotherapy through study completion, every three months.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Sep 2026.

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