Systemic therapy of skin metastatic melanoma with BRAF gene mutation

Y.S. Shakh-Paronyants, S. Cheporov, N. P. Shiryaev, A. V. Ukgarskiy, P. Nesterov, N. Korzina
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Abstract

Purpose of the study. To conduct a comparative analysis of the effectiveness of the use of mono‑mode immuno‑oncological and targeted drugs in the first line of therapy in patients with metastatic melanoma of the skin (SMM) in patients with BRAF mutation.Patients and methods. To achieve this goal, a retrospective analysis of the treatment results was carried out in 61 patients diagnosed with metastatic melanoma of the skin and the presence of a mutation in the BRAF gene who were treated at the Yaroslavl regional oncology hospital. The patients were divided into two groups: the first group (n = 18) included patients who received mono‑mode immunotherapy in the first line of treatment; the second group (n = 43) included patients who underwent targeted first-line therapy.Standard regimens of monotherapy with BRAF inhibitors (vemurafenib, dabrafenib) or combination therapy with BRAF and MEK inhibitors (dabrafenib + trametinib) were chosen as treatment. Immunotherapy was performed using the following drugs: pembrolizumab, nivolumab and prolgolimab. An intergroup comparative analysis of one‑year, three‑year and five‑year survival rates was carried out. Progression‑free survival rates and the frequency of objective responses were also studied.Results. The median follow–up period in the first group was 14.2 months, in the second – 15.7 months. The indicators of one‑year, three-year and five‑year overall survival in patients receiving immunotherapy in the first line were 88.8 %, 55.5 % and 33.3 %, respectively. The same indicators in patients in the first‑line targeted therapy group were 90.7 %, 46.5 % and 23.2 %, respectively. The median overall survival in the first group was 39.1 months, in the second group it was 30.4 months. Progression–free survival in the group of patients with targeted therapy was 8.7 months, in the immunotherapy group – 9.8 months. In the first group, stabilization of the disease was observed in 77.8 % of patients, while a complete response was noted in 5.6 %, a partial response was not registered. In the second group of patients, stabilization was noted in 39.6 % of patients, partial response in 25.6 % of patients, complete response was absent.Conclusion. The use of cancer immunotherapy drugs in the first line of treatment in patients with metastatic melanoma of the skin and the presence of BRAF mutation in the short term is not inferior in effectiveness to the use of targeted drugs, and in the medium and long term exceeds targeted drugs.
BRAF基因突变皮肤转移性黑色素瘤的全身治疗
研究目的:对BRAF突变的皮肤转移性黑色素瘤(SMM)患者一线治疗中使用单模免疫肿瘤药物和靶向药物的有效性进行比较分析。患者和方法。为了实现这一目标,对在雅罗斯拉夫尔地区肿瘤医院接受治疗的61例被诊断为皮肤转移性黑色素瘤并存在BRAF基因突变的患者的治疗结果进行了回顾性分析。患者被分为两组:第一组(n = 18)包括在一线接受单模免疫治疗的患者;第二组(n = 43)包括接受靶向一线治疗的患者。选择BRAF抑制剂(vemurafenib, dabrafenib)单药治疗或BRAF和MEK抑制剂(dabrafenib + trametinib)联合治疗的标准方案作为治疗。使用以下药物进行免疫治疗:派姆单抗,纳武单抗和prolgolimab。对1年、3年和5年生存率进行组间比较分析。对无进展生存率和客观反应频率也进行了研究。第一组的中位随访时间为14.2个月,第二组为15.7个月。一线接受免疫治疗患者的1年、3年和5年总生存率指标分别为88.8%、55.5%和33.3%。一线靶向治疗组患者的相同指标分别为90.7%、46.5%和23.2%。第一组的中位总生存期为39.1个月,第二组为30.4个月。靶向治疗组患者的无进展生存期为8.7个月,免疫治疗组为9.8个月。在第一组中,77.8%的患者病情稳定,5.6%的患者出现完全缓解,未出现部分缓解。在第二组患者中,39.6%的患者出现稳定,25.6%的患者出现部分缓解,没有完全缓解。对于存在BRAF突变的皮肤转移性黑色素瘤患者,在一线治疗中使用肿瘤免疫治疗药物,短期疗效不逊于使用靶向药物,中长期疗效超过靶向药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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