Suppr超能文献

BRAF 突变型黑色素瘤脑转移患者中 BRAF 抑制和 MEK 抑制的临床及影像学反应

Clinical and radiological response of BRAF inhibition and MEK inhibition in patients with brain metastases from BRAF-mutated melanoma.

作者信息

Geukes Foppen Marnix H, Boogerd Willem, Blank Christian U, van Thienen Johannes V, Haanen John B, Brandsma Dieta

机构信息

Departments of Medical Oncology.

Neuro-Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

Melanoma Res. 2018 Apr;28(2):126-133. doi: 10.1097/CMR.0000000000000429.

Abstract

Patients with brain metastases (BM) from melanoma have an overall survival (OS) of 2-6 months after whole-brain radiotherapy. Targeted therapy (TT) is an effective treatment for BRAF-mutated metastatic melanoma. Moreover, recent studies indicate intracranial responses of TT in patients with BM. We analyzed 146 patients with BM from BRAF-mutated melanoma treated with vemurafenib, dabrafenib, or dabrafenib+trametinib between 2010 and 2016. We determined clinical and radiological response, progression-free survival (PFS), and OS. Median OS of patients treated with dabrafenib+trametinib was 11.2 months [n=30; 95% confidence interval (CI): 6.8-15.7], 8.8 months for dabrafenib alone (n=31; 95% CI: 3.9-13.7), and 5.7 months for vemurafenib (n=85; 95% CI: 4.6-6.8). A significantly longer OS was observed in the dabrafenib+trametinib group than in the vemurafenib group (hazard ratio for death, 0.52; 95% CI: 0.30-0.89; P=0.02). Median intracranial PFS of all patients was 4.1 months. Median intracranial PFS for patients treated with dabrafenib+trametinib was 5.8 months (95% CI: 3.2-8.5), 5.7 months (95% CI: 3.0-8.4) for dabrafenib, and 3.6 months (95% CI: 3.5-3.8) for vemurafenib (P=0.54). A total of 63 (43%) patients had symptomatic BM. Intracranial disease control rate at 8 weeks in these patients was 65 versus 70% extracranially. Neurological symptoms improved in 46% of patients with symptomatic BM, whereas in 21%, they remained stable. Median OS in patients with BM from BRAF-mutated melanoma treated with dabrafenib+trametinib was significantly longer than for vemurafenib. Improvement of neurological symptoms was seen in almost half of the patients with symptomatic BM treated with TT.

摘要

黑色素瘤脑转移(BM)患者在全脑放疗后的总生存期(OS)为2至6个月。靶向治疗(TT)是BRAF突变转移性黑色素瘤的有效治疗方法。此外,最近的研究表明TT对BM患者有颅内反应。我们分析了2010年至2016年间146例接受维莫非尼、达拉非尼或达拉非尼+曲美替尼治疗的BRAF突变黑色素瘤脑转移患者。我们确定了临床和影像学反应、无进展生存期(PFS)和总生存期。接受达拉非尼+曲美替尼治疗患者的中位总生存期为11.2个月[n = 30;95%置信区间(CI):6.8 - 15.7],单独使用达拉非尼的患者为8.8个月(n = 31;95% CI:3.9 - 13.7),维莫非尼治疗的患者为5.7个月(n = 85;95% CI:4.6 - 6.8)。达拉非尼+曲美替尼组的总生存期显著长于维莫非尼组(死亡风险比,0.52;95% CI:0.30 - 0.89;P = 0.02)。所有患者的中位颅内无进展生存期为4.1个月。接受达拉非尼+曲美替尼治疗患者的中位颅内无进展生存期为5.8个月(95% CI:3.2 - 8.5),达拉非尼为5.7个月(95% CI:3.0 - 8.4),维莫非尼为3.6个月(95% CI:3.5 - 3.8)(P = 0.54)。共有63例(43%)患者有症状性脑转移。这些患者在8周时的颅内疾病控制率为65%,颅外为70%。46%有症状性脑转移的患者神经症状改善,而21%的患者神经症状保持稳定。接受达拉非尼+曲美替尼治疗的BRAF突变黑色素瘤脑转移患者的中位总生存期显著长于维莫非尼治疗的患者。在接受TT治疗的有症状性脑转移患者中,近一半患者的神经症状得到改善。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验