Phase
Condition
Melanoma
Treatment
Radiation Therapy
Quality-of-Life Assessment
Immunotherapy
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Must be planned for post-operative immunotherapy
No evidence of distant metastasis as determined by clinical examination and any formof imaging
No evidence of clinically involved lymph nodes prior to SLNB
Pathologically confirmed sentinel lymph node positive melanoma with high riskfeatures (extracapsular extension [ECE] or 0.5 mm+ nodal tumor implant or 2+involved nodes or lymphovascular invasion of the primary tumor)
Has provided written informed consent for participation in this trial
Eastern Cooperative Oncology Group (ECOG) performance status of 3 or less
Life expectancy greater than 6 months
Patients capable of childbearing are using adequate contraception
Available for follow-up
Exclusion
Exclusion Criteria:
Complete lymph node dissection (CLND) of the nodal basin containing the positive SLN
Distant metastasis
Previous radiation therapy (RT) to the nodal area planned for RT such that the priorRT field would be included in the current treatment field. In other words, treatmenton this trial would require re-irradiation of tissues
Women who are pregnant
Adults unable to consent, individuals who are not yet adults, pregnant women andprisoners will be excluded from this study
Study Design
Study Description
Connect with a study center
Baptist - MD Anderson Cancer Center
Jacksonville, Florida 32207
United StatesActive - Recruiting
Cooper Hospital UNIV MED CTR.
Camden, New Jersey 08103
United StatesActive - Recruiting
M D Anderson Cancer Center
Houston, Texas 77030
United StatesActive - Recruiting
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