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BRAF和MEK联合抑制与立体定向放射外科治疗BRAF突变型黑色素瘤脑转移的初步经验。

Initial experience with combined BRAF and MEK inhibition with stereotactic radiosurgery for BRAF mutant melanoma brain metastases.

作者信息

Patel Bindiya G, Ahmed Kamran A, Johnstone Peter A S, Yu Hsiang-Hsuan Michael, Etame Arnold B

机构信息

aMorsani College of Medicine, University of South Florida Departments of bRadiation Oncology cNeuro-Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.

出版信息

Melanoma Res. 2016 Aug;26(4):382-6. doi: 10.1097/CMR.0000000000000250.

Abstract

The combined use of the BRAF inhibitor dabrafenib and MEK inhibitor trametinib has been found to improve survival over dabrafenib alone. The management of melanoma brain metastases continues to present challenges. In this study, we report our initial experience in the management of melanoma brain metastases with stereotactic radiosurgery (SRS) with the use of BRAF and MEK inhibitors. We identified six patients treated with SRS for 17 brain metastases within 3 months of BRAF and MEK inhibitor administration. The median planning target volume was 0.42 cm (range: 0.078-2.08 cm). The median treatment dose was 21 Gy (range 18-24 Gy). The median follow-up of all lesions from SRS was 10.6 months (range 5.8-28.5 months). One lesion was found to undergo local failure 21.7 months following SRS treatment. The median overall survival was 20.0 months (range 6.1-31.8 months) from the time of SRS treatment and 23.1 months (range: 12.1-30.9 months) from the date of BRAFi and MEKi administration. There was no evidence of increased nor unexpected toxicity with the two modalities combined. In this initial experience of melanoma brain metastases treated with BRAF and MEK inhibition with SRS, we find the two modalities can be combined safely. These outcomes should be assessed further in prospective evaluations.

摘要

已发现BRAF抑制剂达拉非尼和MEK抑制剂曲美替尼联合使用比单独使用达拉非尼能提高生存率。黑色素瘤脑转移的管理仍然面临挑战。在本研究中,我们报告了使用BRAF和MEK抑制剂进行立体定向放射外科治疗(SRS)管理黑色素瘤脑转移的初步经验。我们确定了6例在使用BRAF和MEK抑制剂后3个月内接受SRS治疗17个脑转移灶的患者。计划靶体积中位数为0.42 cm(范围:0.078 - 2.08 cm)。治疗剂量中位数为21 Gy(范围18 - 24 Gy)。SRS治疗后所有病灶的中位随访时间为10.6个月(范围5.8 - 28.5个月)。发现1个病灶在SRS治疗后21.7个月出现局部复发。从SRS治疗时起的中位总生存期为20.0个月(范围6.1 - 31.8个月),从BRAF抑制剂和MEK抑制剂给药日期起为23.1个月(范围:12.1 - 30.9个月)。没有证据表明两种方法联合使用会增加毒性或出现意外毒性。在使用BRAF和MEK抑制剂联合SRS治疗黑色素瘤脑转移的这一初步经验中,我们发现这两种方法可以安全联合使用。这些结果应在前瞻性评估中进一步评估。

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