Stereotactic Radiosurgery and Anti-PD-1 + CTLA-4 Therapy, Anti-PD-1 Therapy, Anti-CTLA-4 Therapy, BRAF/MEK Inhibitors, BRAF Inhibitors, or Conventional Chemotherapy for the Management of Melanoma Brain Metastases
Menée à partir de données portant sur 257 patients traités, sur la période 2011-2020, pour des métastases cérébrales ayant pour origine un mélanome (durée médiane de suivi : 42 mois après traitement), cette étude évalue l'efficacité, du point de vue de la survie globale, d'une radiochirurgie en combinaison avec une thérapie ciblée ou une immunothérapie
Background: Immunotherapy and targeted BRAF/MEK inhibitors (i) have revolutionized the systemic management of advanced melanoma. Given the role of stereotactic radiosurgery (SRS) in the local management of brain metastases, we sought to evaluate clinical outcomes in patients with melanoma brain metastases (MBM) treated with SRS and various systemic therapies. Methods: Patients were included if MBM were diagnosed and treated with SRS within 3 months of receiving anti-PD-1 + CTLA-4 therapy, anti-PD-1 therapy, anti-CTLA-4 therapy, BRAF/MEK-i, BRAF-i, or conventional chemotherapy. Comparisons between groups were made for overall survival (OS), distant MBM control, local MBM, systemic progression free survival (sPFS) and neurotoxicity. Results: In total, 257 patients with 1048 MBM treated over 368 SRS sessions between 2011 to 2020 were identified. On MVA treatment with anti-PD1 + anti-CTLA-4, anti-PD-1, and BRAF/MEK-i improved DIC over conventional chemotherapy. No significant differences were noted in local control between groups (p=0.78). Kaplan-Meier OS at 12 months for anti-PD-1 + CTLA-4 therapy, anti-PD-1 therapy, anti-CTLA-4 therapy, BRAF/MEK-i, BRAF-i, and conventional chemotherapy was 68%, 59%, 45%, 62%, 21%, and 15% respectively (p = <0.0001). The sPFS rates at 12 months were 57%, 53%, 42%, 45%, 14%, and 6% (p = <0.0001). No significant differences were noted in rates of radiation necrosis (p=0.93). Conclusions: This is among the largest series evaluating MBM treated with SRS and various systemic therapy regimens. Our analysis noted significant differences in OS, distant MBM control, and sPFS by systemic therapy. No differences in local control or radiation necrosis risk were noted.