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NCT07924969Completed

Hypofractionated Whole-Brain Radiotherapy in the Treatment of Disseminated Cutaneous and Mucosal Melanoma Patients With Multiple Brain Metastases.

Phase II Randomized Clinical Trial. Hypofractionated Whole-Brain Radiotherapy in the Treatment of Disseminated Cutaneous and Mucosal Melanoma Patients With Multiple Brain Metastases.

Source: ClinicalTrials.gov · Last updated 9 Nov 2026

Next steps

Brief summary (registry, in English)

The goal of this clinical trial is to compare an extreme hypofractionation regimen (6.5 Gy per fraction, total 26 Gy) with standard fractionation (3 Gy per fraction, total 30 Gy) for WBRT in patients with multiple melanoma brain metastases. The main questions it aims to answer are: Does hypofractionated WBRT increases OS? How effective is the hypofractionation regimen in local control compared to the standart fractionation? Will the toxicity increase? Will the quality of life increase in an experimental group?

Status (registry)
Completed
Study type
Interventional
Enrollment
50 (actual)
First submitted
16 Oct 2026
Start date
1 Jul 2022
Primary completion date
1 Apr 2026
Lead sponsor
National Medical Research Radiological Centre of the Ministry of Health of Russia
Diseases
Melanoma
NCT number
NCT07924969

What you commit to

  • Study type: Interventional
  • Participants enrolled: 50
  • From 1 Jul 2022 to the primary completion date, 1 Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • prior brain radiotherapy

Other illness

  • severe somatic condition
  • psychiatric disorders.

Other

  • pregnancy

Who the study is looking for

  • Multiple brain metastases (≥5 lesions, or fewer if stereotactic radiosurgery is not indicated)
  • Age >18 years
  • Morphologically verified primary tumor (for unknown primary, verification of metastatic lesion required)
  • Signed informed consent
  • Karnofsky Performance Status ≥60%
  • Any life expectancy (any GPA score)
  • No contraindications to external-beam radiotherapy

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
P.A. Hertsen Moscow Oncology Research Center Branch of FSBI NMRRC of the Ministry of Health of RussiaMoscowRussiaUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.