Stera Susanne, Balermpas Panagiotis, Blanck Oliver, Wolff Robert, Wurster Stefan, Baumann Rene, Szücs Marcella, Loutfi-Krauss Britta, Wilhelm Maria-Lisa, Seifert Volker, Rades Dirk, Rödel Claus, Dunst Jürgen, Hildebrandt Guido, Arnold Andreas, Meissner Markus, Kähler Katharina C
Departments of Radiation Oncology.
Saphir Radiosurgery Center, Frankfurt and Northern Germany, Güstrow, Germany.
Melanoma Res. 2019 Apr;29(2):187-195. doi: 10.1097/CMR.0000000000000542.
The aim was to evaluate toxicity and oncological outcome of combined stereotactic radiosurgery (SRS) and immunotherapy or targeted therapy in patients with multiple brain metastases originating from malignant melanoma. Despite the fact that both SRS and kinase inhibitors or immune checkpoint inhibitors are considered standard treatment options for this indication, the optimal combination and sequence of these modalities remains largely unknown, especially for patients with a high number of brain metastases. For this retrospective analysis, conducted in two large SRS dedicated centers, we identified patients with brain metastases from malignant melanoma and simultaneous application of immunotherapy or targeted therapy within 30 days of SRS. Forty-eight patients with a total of 250 lesions (median: 3) were treated in 65 single fraction SRS sessions from 2012 to 2018. After a median follow-up of 8.3 months (range: 1.2-43.6 months), the 6-month and 1-year overall survival rates were 75.3 and 50.8%, respectively. The local control rate at one year was 89.5%. Immunotherapy and the application of systemic treatment directly before or concomitant to SRS were both associated with improved overall survival (P=0.037 and 0.045, respectively). We observed four grade III toxicities, of which only two can be clearly attributed to the combined treatment. Various combinations of SRS and kinase inhibitors or immune checkpoint inhibitors appear feasible and provide promising oncological results and safety profiles for treating few (n=1-4) and also multiple (n≥5) melanoma brain metastases.
目的是评估立体定向放射外科(SRS)联合免疫疗法或靶向疗法对恶性黑色素瘤多发脑转移患者的毒性和肿瘤学结局。尽管SRS与激酶抑制剂或免疫检查点抑制剂均被视为该适应症的标准治疗选择,但这些治疗方式的最佳组合和顺序仍 largely unknown,尤其是对于脑转移数量较多的患者。在两个大型SRS专门中心进行的这项回顾性分析中,我们确定了患有恶性黑色素瘤脑转移且在SRS后30天内同时应用免疫疗法或靶向疗法的患者。2012年至2018年期间,共48例患者(总计250个病灶,中位数:3个)接受了65次单次分割SRS治疗。中位随访8.3个月(范围:1.2 - 43.6个月)后,6个月和1年的总生存率分别为75.3%和50.8%。1年时的局部控制率为89.5%。免疫疗法以及在SRS之前或同时进行全身治疗均与总生存率提高相关(分别为P = 0.037和0.045)。我们观察到4例3级毒性反应,其中仅有2例可明确归因于联合治疗。SRS与激酶抑制剂或免疫检查点抑制剂的各种组合似乎可行,并为治疗少数(n = 1 - 4)以及多发(n≥5)黑色素瘤脑转移提供了有前景的肿瘤学结果和安全性概况。