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Stereotactic radiosurgery combined with nivolumab or Ipilimumab for patients with melanoma brain metastases: evaluation of brain control and toxicity
by
Cappellini, Gian Carlo Antonini
, Minniti, Giuseppe
, Reverberi, Chiara
, Bozzao, Alessandro
, Marchetti, Luca
, Esposito, Vincenzo
, Osti, Mattia
, Anzellini, Dimitri
, Bianciardi, Federico
, Gentile, Pier Carlo
in
Brain cancer
/ Cancer
/ Cancer metastasis
/ Cancer treatment
/ Care and treatment
/ checkpoint inhibitors
/ Clinical/Translational Cancer Immunotherapy
/ Dosage and administration
/ Edema
/ fractionated stereotactic radiosurgery
/ Immunology
/ Immunotherapy
/ Ipilimumab
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Melanoma
/ melanoma brain metastases
/ Metastasis
/ Monoclonal antibodies
/ Multivariate analysis
/ Necrosis
/ Nivolumab
/ Oncology
/ Patients
/ Radiation
/ Radiation (Physics)
/ Radiosurgery
/ Radiotherapy
/ Research Article
/ stereotactic radiosurgery
/ Surgery
/ Targeted cancer therapy
/ Toxicity
/ Tumors
/ Variables
2019
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Stereotactic radiosurgery combined with nivolumab or Ipilimumab for patients with melanoma brain metastases: evaluation of brain control and toxicity
by
Cappellini, Gian Carlo Antonini
, Minniti, Giuseppe
, Reverberi, Chiara
, Bozzao, Alessandro
, Marchetti, Luca
, Esposito, Vincenzo
, Osti, Mattia
, Anzellini, Dimitri
, Bianciardi, Federico
, Gentile, Pier Carlo
in
Brain cancer
/ Cancer
/ Cancer metastasis
/ Cancer treatment
/ Care and treatment
/ checkpoint inhibitors
/ Clinical/Translational Cancer Immunotherapy
/ Dosage and administration
/ Edema
/ fractionated stereotactic radiosurgery
/ Immunology
/ Immunotherapy
/ Ipilimumab
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Melanoma
/ melanoma brain metastases
/ Metastasis
/ Monoclonal antibodies
/ Multivariate analysis
/ Necrosis
/ Nivolumab
/ Oncology
/ Patients
/ Radiation
/ Radiation (Physics)
/ Radiosurgery
/ Radiotherapy
/ Research Article
/ stereotactic radiosurgery
/ Surgery
/ Targeted cancer therapy
/ Toxicity
/ Tumors
/ Variables
2019
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Stereotactic radiosurgery combined with nivolumab or Ipilimumab for patients with melanoma brain metastases: evaluation of brain control and toxicity
by
Cappellini, Gian Carlo Antonini
, Minniti, Giuseppe
, Reverberi, Chiara
, Bozzao, Alessandro
, Marchetti, Luca
, Esposito, Vincenzo
, Osti, Mattia
, Anzellini, Dimitri
, Bianciardi, Federico
, Gentile, Pier Carlo
in
Brain cancer
/ Cancer
/ Cancer metastasis
/ Cancer treatment
/ Care and treatment
/ checkpoint inhibitors
/ Clinical/Translational Cancer Immunotherapy
/ Dosage and administration
/ Edema
/ fractionated stereotactic radiosurgery
/ Immunology
/ Immunotherapy
/ Ipilimumab
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Melanoma
/ melanoma brain metastases
/ Metastasis
/ Monoclonal antibodies
/ Multivariate analysis
/ Necrosis
/ Nivolumab
/ Oncology
/ Patients
/ Radiation
/ Radiation (Physics)
/ Radiosurgery
/ Radiotherapy
/ Research Article
/ stereotactic radiosurgery
/ Surgery
/ Targeted cancer therapy
/ Toxicity
/ Tumors
/ Variables
2019
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Stereotactic radiosurgery combined with nivolumab or Ipilimumab for patients with melanoma brain metastases: evaluation of brain control and toxicity
Journal Article
Stereotactic radiosurgery combined with nivolumab or Ipilimumab for patients with melanoma brain metastases: evaluation of brain control and toxicity
2019
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Overview
Purpose
To investigate the efficacy and safety of concurrent stereotactic radiosurgery (SRS) and ipilimumab or nivolumab in patients with untreated melanoma brain metastases.
Patients and Methods
Eighty consecutive patients with 326 melanoma brain metastases receiving SRS in combination with ipilimumab or nivolumab were identified from an institutional database and retrospectively evaluated. Patients started systemic treatment with intravenous nivolumab or ipilimumab within one week of receiving SRS. Nivolumab was given at doses of 3 mg/kg every two weeks. Ipilimumab was administered up to four doses of 10 mg/kg, one every 3 weeks, then patients had a maintenance dose of 10 mg/kg every 12 weeks, until disease progression or inacceptable toxicity. Primary endpoint of the study was intracranial progression-free survival (PFS). Secondary endpoints were extracranial PFS, overall survival (OS), and neurological toxicity.
Results
Eighty patients were analyzed. Forty-five patients received SRS and ipilimumab, and 35 patients received SRS and nivolumab. With a median follow-up of 15 months, the 6-month and 12-month intracranial PFS rates were 69% (95%CI,54–87%) and 42% (95%CI,24–65%) for patients receiving SRS and nivolumab and 48% (95%CI,34–64%) and 17% (95%CI,5–31%) for those treated with SRS and ipilimumab (p = 0.02), respectively. Extracranial PFS and OS were 37 and 78% in SRS and nivolumab group, respectively, and 17 and 68% in SRS and ipilimumab group, respectively, at 12 months. Sub-group analysis showed significantly better intracranial PFS for patients receiving multi-fraction SRS (3 × 9 Gy) compared to single-fraction SRS (70% versus 46% at 6 months,
p
= 0.01), especially in combination with nivolumab. Grade 3 treatment-related adverse events occurred in 11 (24%) patients treated with SRS and ipilimumab and 6 (17%) patients who received SRS and nivolumab. Radiation-induced brain necrosis (RN) occurred in 15% of patients.
Conclusions
Concurrent SRS and ipilimumab or nivolumab show meaningful intracranial activity in patients with either asymptomatic and symptomatic melanoma brain metastases, although a subset of patients may develop symptomatic RN. The combination of nivolumab with SRS is associated with better intracranial control.
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