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黑色素瘤脑转移立体定向放射治疗后放射性坏死的发生率:免疫治疗的潜在影响。

The incidence of radiation necrosis following stereotactic radiotherapy for melanoma brain metastases: the potential impact of immunotherapy.

作者信息

Kaidar-Person Orit, Zagar Timothy M, Deal Allison, Moschos Stergios J, Ewend Matthew G, Sasaki-Adams Deanna, Lee Carrie B, Collichio Frances A, Fried David, Marks Lawrence B, Chera Bhishamjit S

机构信息

aUNC Lineberger Comprehensive Cancer Center Departments of bRadiation Oncology cMedicine dNeurosurgery, University of North Carolina, Chapel Hill, North Carolina, USA.

出版信息

Anticancer Drugs. 2017 Jul;28(6):669-675. doi: 10.1097/CAD.0000000000000497.

Abstract

Stereotactic radiotherapy (SRT) is the standard treatment for patients with limited number of brain metastases. In the past few years, newer immunotherapies (immune checkpoint inhibitors) have been proven to prolong survival in patients with metastatic melanoma. The safety of the combination of SRT and immunotherapy for brain metastases is unknown. We retrospectively identified patients with melanoma brain metastases treated with SRT between 2007 and 2015. Patients who did not have at least 3 months of follow-up with imaging after SRT were excluded from the analysis. Outcomes were compared between patients who were treated with or without immunotherapy. A total of 58 patients were included; of these, 29 were treated with SRT and immunotherapy. MAPK inhibitors (BRAF, MEK inhibitors) were used more often in the immunotherapy group (nine vs. two patients). There was a higher incidence of intracranial complications in patients treated with immunotherapy and SRT. Eight patients had radiation necrosis; all occurred in patients who were treated with immunotherapy. Nine patients had hemorrhage, of which seven occurred in patients who were treated with immunotherapy (P=0.08). However, patients treated with immunotherapy and SRT had a significant overall survival advantage compared with SRT without immunotherapy (15 vs. 6 months, P=0.0013). Patients treated with SRT and immunotherapy have a higher incidence/risk of intracranial complications, but a longer overall survival.

摘要

立体定向放射治疗(SRT)是脑转移瘤数量有限患者的标准治疗方法。在过去几年中,新型免疫疗法(免疫检查点抑制剂)已被证明可延长转移性黑色素瘤患者的生存期。SRT与免疫疗法联合用于脑转移瘤的安全性尚不清楚。我们回顾性地确定了2007年至2015年间接受SRT治疗的黑色素瘤脑转移患者。SRT后未进行至少3个月影像学随访的患者被排除在分析之外。比较接受或未接受免疫疗法治疗的患者的结局。共纳入58例患者;其中29例接受了SRT和免疫疗法治疗。免疫疗法组更常使用MAPK抑制剂(BRAF、MEK抑制剂)(9例对2例)。接受免疫疗法和SRT治疗的患者颅内并发症发生率更高。8例患者发生放射性坏死;均发生在接受免疫疗法治疗的患者中。9例患者发生出血,其中7例发生在接受免疫疗法治疗的患者中(P=0.08)。然而,与未接受免疫疗法的SRT相比,接受免疫疗法和SRT治疗的患者具有显著的总生存优势(15个月对6个月,P=0.0013)。接受SRT和免疫疗法治疗的患者颅内并发症发生率/风险更高,但总生存期更长。

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