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Pigment Cell Melanoma Res ; 32(4): 553-563, 2019 07.
Article in English | MEDLINE | ID: mdl-30767428

ABSTRACT

BACKGROUND: Brain radiotherapy is used in the management of melanoma brain metastases (MBM) and can result in radionecrosis. Anti-PD-1 is active in the brain and may increase the risk of radionecrosis when combined with radiotherapy. We studied the incidence, associated factors and management of radionecrosis in longer-term survivors with MBM treated with this combination. METHODS: Patients with MBM treated with radiotherapy and anti-PD-1 who survived >1 year were identified to determine radionecrosis incidence (Cohort A, n = 135). Cohort A plus additional radionecrosis cases were examined for factors associated with radionecrosis and management (Cohort B, n = 148). RESULTS: From Cohort A, 17% developed radionecrosis, with a cumulative incidence at 2 years of 18%. Using Cohort B, multivariable analysis confirmed an association between radionecrosis and elevated lactate dehydrogenase (p = 0.0496) and prior treatment with ipilimumab (p = 0.0319). Radionecrosis was diagnosed based on MRI (100%), symptoms (69%) and pathology (56%). Treatment included corticosteroids, bevacizumab and neurosurgery. CONCLUSIONS: Radionecrosis is a significant toxicity in longer-term melanoma survivors with MBM treated with anti-PD-1 and radiotherapy. Identification of those at risk of radionecrosis who may avoid radiotherapy is required.


Subject(s)
Antibodies/therapeutic use , Brain/radiation effects , Melanoma/immunology , Melanoma/radiotherapy , Programmed Cell Death 1 Receptor/immunology , Radiation Injuries/epidemiology , Radiation Injuries/etiology , Cohort Studies , Female , Humans , Incidence , Magnetic Resonance Imaging , Male , Melanoma/diagnostic imaging , Middle Aged , Multivariate Analysis , Necrosis , Radiation Injuries/diagnostic imaging , Radiation Injuries/surgery , Risk Factors , Survival Analysis
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